Architecture for Health Initiative (Arch4Health): Computational Challenges in Health-Related Applications and the Role of Computer Architecture in Addressing Them Nika Mansouri Ghiasi* ETH Zürich Switzerland
Konstantina Koliogeorgi* ETH Zürich Switzerland
arXiv:2606.22685v1 [cs.AR] 21 Jun 2026
Abstract Recent biotechnological advances enable high-throughput, lowcost, and accurate biological data generation. This wealth of data enables unique opportunities for advancing healthcare. Despite these opportunities, efficiently analyzing large-scale biological data poses significant challenges for conventional computing systems. These systems often cannot keep up with the high-throughput rate at which data is generated, and they face additional constraints related to energy efficiency, scalability, privacy, and security. Therefore, to facilitate the wide adoption of recent advances in healthcare, there is a need to optimize the computing systems to enable highperformance, energy-efficient, low-cost, private, and secure analysis of biological data. We introduce the Architecture for Health (Arch4Health) initiative, which aims to (i) identify and analyze key computational challenges in current and future health- and life science-related applications and (ii) explore how computer architects and computing system designers can advance healthcare by addressing these challenges. In this short paper, we first present the motivations behind the Arch4Health initiative and, second, elaborate on its vision and goals, related topics, Arch4Health workshops, and future outlooks.
1
Motivation
Recent advances in biotechnology and sensing technologies have enabled high-throughput, low-cost, and accurate biological data generation. Modern sequencing platforms [1–33] and other omics technologies [34] can generate massive amounts of biological data (genomics [35–88, 88–109], transcriptomics [110–121], proteomics [122–127], and metabolomics [128–132]) at rapidly decreasing costs. Similarly, multimodal medical imaging technologies [133–138] produce high-resolution data that capture complex physiological and pathological processes. Wearable and implantable sensing devices [139–143] continuously monitor physiological signals such as heart activity, glucose levels, oxygen saturation in real time. Together, these advances have created an unprecedented volume of heterogeneous health- and life science-related data. This wealth of data creates unique opportunities for advancing healthcare and biomedical discovery, such as precision medicine [144–151], where treatments and therapeutic strategies can be tailored to the genetic and physiological characteristics of individual patients. Large-scale genomic and clinical datasets also advance personalized medicine [144–146, 148–172], tracking outbreaks of communicable diseases [173–198], cancer research [199– 245], bedside personalized care [246], agriculture [247–262], ensuring food safety [263, 264], scientific discovery [265–267], biodiversity conservation [268, 269], evolutionary biology [270–287]. Continuous physiological monitoring via wearable sensors further ∗ Both authors contributed equally to this paper.
Onur Mutlu ETH Zürich Switzerland
enables proactive and preventive healthcare by enabling early detection of anomalies [288] and timely clinical intervention [289, 290]. Despite these opportunities, efficiently analyzing large-scale biological data poses significant challenges for conventional computing systems. First, these systems often cannot keep up with the highthroughput rate at which data is generated. For example, modern sequencing platforms can generate data at rates that create substantial computational bottlenecks in downstream analysis, including sequence alignment and variant calling [36, 291–296]. Similarly, images are generated at a pace that exceeds the throughput of image reconstruction analytics and machine learning-based inference. High-throughput processing is crucial in clinical settings, where real-time data processing can significantly impact patient outcomes by improving both response times in time-critical scenarios and the decision-making processes for therapeutic schemes [297]. Second, health- and life science-related applications suffer from data movement overheads [36, 37, 43–48, 79–84, 298–317]. These workloads frequently involve irregular memory access patterns [309, 318–320], massive data transfer overheads [91, 321], complex graph and statistical computations [322, 323], and often rely on computationally intensive machine learning models [324]. As a result, data movement often dominates execution time and energy consumption. As datasets continue to grow in size and complexity, this bottleneck is further exacerbated [325]. Growing adoption of deep learning models is also expected to amplify these challenges by requiring frequent movement of large model parameters and intermediate data across the computing stack [326]. Third, systems must process sensitive patient data while satisfying strict privacy and regulatory requirements for health applications [327, 328]. Hospitals, portable diagnostic devices and wearable platforms need to meet such requirements through secure data storage, trusted computation, federated learning, and privacy-preserving analytics [329–332]. These challenges motivate the need for a closer collaboration between the health- and life science-related domain (e.g., clinical and precision medicine, omics research, genetics, computational biology, drug discovery, public health, and epidemiology), computer architecture, and computing systems design communities. Advancing healthcare applications requires rethinking computing system design across the entire stack, including hardware accelerators, memory hierarchies, storage systems, data movement mechanisms, distributed infrastructures, and privacy-aware architectures. Prior work has already demonstrated the promise of this direction. A growing body of computer architecture research has proposed algorithmic optimizations (e.g., [88, 94–109, 333–351]) or hardware accelerators (e.g., [35–93, 304, 309, 346, 352–380]), and/or reducing data movement overheads [313–316, 381] via near-data processing
(e.g., in main memory [43–48, 79–84, 298–304, 382–385] or storage [81, 305–311, 386–391]) for workloads such as genome sequence analysis, metagenomic profiling, medical imaging, real-time physiological monitoring and biological simulation, providing substantial improvements in performance, energy efficiency, and scalability over conventional CPU- and GPU-based pipelines. Despite these promising advances, significant challenges remain unresolved and even bigger strides are necessary. Computer architecture research, done collaboratively with experts in healthcare and life sciences, can play a key role in addressing these challenges and in enabling high-performance, energy-efficient, secure, and scalable computing systems for healthcare and life sciences.
2
The Arch4Health Initiative
Vision and Goals. We introduce the Architecture for Health (Arch4Health) initiative, which aims to (i) identify key computational challenges in current and future health- and life sciencerelated applications and (ii) explore how computer architects and computing system designers can advance healthcare by addressing these challenges. Since cross-disciplinary discussions are crucial for better identifying and solving challenges in real-world health- and life science-related applications, we aim to foster open discussions and cooperation between researchers with diverse backgrounds (i.e., from both computer architecture and health sciences communities, industry, and academia). Topics. Arch4Health invites contributions and collaborations on a broad range of topics at the intersection of computer architecture and health- and life science-related applications. These topics include, but are not limited to, computational biology (e.g., genomics, metagenomics, transcriptomics, single-cell analysis, spatial omics, proteomics, drug design and discovery, gene editing, and other areas in precision medicine and public health), neuroscience (e.g., brain-machine interfaces and prosthetics), wearable systems for health, medical robotics (e.g., surgery and haptics), mental health, medical imaging (e.g., brain scans, radiology, and single-cell analysis), computational and digital pathology, artificial intelligence and foundation models for biology and health (e.g., protein language models, cell foundation models, and large language models for clinical applications), agent-based simulations, medical privacy, and bio-sensors. We particularly welcome contributions that identify computational challenges in these domains and propose new ideas (architectures and systems together with algorithms) to improve performance, energy efficiency, cost-effectiveness, and privacy. Arch4Health Workshops. The primary instrument through which Arch4Health currently pursues its goals is a series of workshops co-located with various computer architecture and computing systems conferences. These workshops are designed to bring together researchers and practitioners from both the computer architecture and systems community and the broader biomedical and healthcare communities in a single venue, and to encourage substantive technical exchange and visibility. To this end, each workshop combines two complementary components. First, the workshops provide invited talks and keynotes that summarize (i) a series of research in computing system designs for healthcare applications and (ii) new ideas and directions in data-intensive healthcare applications. Second, the workshops invite researchers to submit their
ongoing work on these topics, with a focus on new ideas. Third, all workshops are livestreamed and available on YouTube [392–394] to enable online, broad and unrestricted access to the entire world. The first two editions of Arch4Health were held in conjunction with the IEEE/ACM International Symposium on Microarchitecture (MICRO) 2025 in Seoul and the IEEE International Symposium on High-Performance Computer Architecture (HPCA) 2026 in Sydney, and together they engaged a broad community spanning computer architecture, bioinformatics, and biomedical research. The MICRO 2025 edition [393, 395] featured ten invited talks covering new algorithms, software, and hardware designs for brain-computer interfaces, medical wearables, genomics, metagenomics, proteomics, and agent-based simulation in life sciences. The HPCA 2026 edition [394, 396] expanded the program to a full-day format with ten talks covering new algorithms, software, and hardware designs for genomics and metagenomics, electrical signals in genomics, AI and algorithms in biology, and indexing and querying petabyte-scale biological sequences. Across both editions, speakers came from a diverse set of academic and research institutions around the world. The next edition of Arch4Health [397] will be held in conjunction with the ACM International Conference on Supercomputing (ICS) 2026 in Belfast, Northern Ireland, United Kingdom. This edition further expands the workshop series by fostering interdisciplinary collaboration among computer architecture, high-performance computing, and health and life science communities. The workshop program features invited talks and discussions on emerging algorithms for genome analysis, scalable architectures, hardware-software codesign for proteomics and genomics and real-time monitoring in clinical environments. We hope this edition will further solidify the importance of the initiative and lead to exciting synergies and research directions. Building on the success of the Arch4Health [395, 396] workshop series, we are expanding the scope toward the system software and system design domain by organizing the Sys4Health workshop [398], co-located with the 32nd Symposium on Operating Systems Principles conference (SOSP 2026). Sys4Health aims to bring together the systems and health and life sciences communities to explore how systems and software infrastructure can enable scalable, secure, and efficient health and life science applications. Future Outlook and a Call to Action. The challenges and opportunities at the intersection of computer architecture and healthand life science-related domains are broad and pressing. Therefore, realizing the vision and goals of Arch4Health requires diverse and cross-disciplinary discussions. We invite computer architects and computing system designers to view health-related applications as a rich and important domain for architectural innovation, and we invite biomedical researchers and clinicians to engage with the architecture community in shaping the systems that will support the next generation of healthcare. Arch4Health is intended to grow as an open and inclusive initiative. We welcome contributions, ideas, and collaborations across multiple communities. Engagement and synergy between both academia and industry is essential to identify key challenges and pave the way toward impactful, practical solutions. Through continued workshops, joint research efforts, and community-building activities, we hope Arch4Health will help grow architecture for
health as a key area of computer architecture, whose advances translate into substantial impact in advancing healthcare and life sciences.
Acknowledgments This paper reflects the vision, objectives, and activities of the Architecture for Health (Arch4Health) workshop initiative. We thank the SAFARI Research Group members for providing a stimulating intellectual and scientific environment. We acknowledge the generous gifts from our industrial partners, including Google, Huawei, Intel, and Microsoft. This work, along with our broader work in studying and accelerating health- and life-science-related applications (e.g., [36, 37, 40, 79, 81, 82, 92, 93, 259, 292, 304, 307, 311, 313, 314, 346, 348–351, 381, 382, 384, 386, 390, 399–421]), is supported in part by the European Union’s Horizon Program for research and innovation under Grant No. 101047160 (project BioPIM), the Swiss National Science Foundation (SNSF) under Grant No. 213084, the Semiconductor Research Corporation (SRC), the ETH Future Computing Laboratory (EFCL), ACCESS – AI Chip Center for Emerging Smart Systems, and the Microsoft Swiss Joint Research Center. No AI or LLM help was used in creating this work.
References [1] David R. Bentley, Shankar Balasubramanian, Harold P. Swerdlow, and others. Accurate whole human genome sequencing using reversible terminator chemistry. In Nature 2008. [2] Marcel Margulies, Michael Egholm, William E. Altman, and others. Genome sequencing in microfabricated high-density picolitre reactors. In Nature 2005. [3] Jay Shendure, Gregory J. Porreca, Nikos B. Reppas, and others. Accurate Multiplex Polony Sequencing of an Evolved Bacterial Genome. In Science 2005. [4] Timothy D. Harris, Phillip R. Buzby, Hazen Babcock, and others. Single-Molecule DNA Sequencing of a Viral Genome. In Science 2008. [5] Gerardo Turcatti, Anthony Romieu, Milan Fedurco, and Ana-Paula Tairi. A new class of cleavable fluorescent nucleotides: synthesis and optimization as reversible terminators for DNA sequencing by synthesis †. In Nucleic Acids Research 2008. [6] Weidong Wu, Brian P. Stupi, Vladislav A. Litosh, and others. Termination of DNA synthesis by N6 -alkylated, not 3’- O -alkylated, photocleavable 2’deoxyadenosine triphosphates. In Nucleic Acids Research 2007. [7] Carl W Fuller. Rapid parallel nucleic acid analysis. US Patent US7264934B2. 2007. [8] Kevin McKernan, Alan Blanchard, Lev Kotler, and Gina Costa. Reagents, methods, and libraries for bead-based sequencing. US Patent US20090181860A1. 2008. [9] Carl W Fuller and John R Nelson. Method for nucleic acid analysis. US Patent US7871771B2. 2011. [10] John Eid, Adrian Fehr, Jeremy Gray, and others. Real-Time DNA Sequencing from Single Polymerase Molecules. In Science 2009. [11] Gianfranco Menestrina. Ionic channels formed byStaphylococcus aureus alphatoxin: Voltage-dependent inhibition by divalent and trivalent cations. In The Journal of Membrane Biology 1986. [12] Gerald M Cherf, Kate R Lieberman, Hytham Rashid, and others. Automated forward and reverse ratcheting of DNA in a nanopore at 5-Å precision. In Nature Biotechnology 2012. [13] Elizabeth A Manrao, Ian M Derrington, Andrew H Laszlo, and others. Reading DNA at single-nucleotide resolution with a mutant MspA nanopore and phi29 DNA polymerase. In Nature Biotechnology 2012. [14] Andrew H Laszlo, Ian M Derrington, Brian C Ross, and others. Decoding long nanopore sequencing reads of natural DNA. In Nature Biotechnology 2014. [15] David Deamer, Mark Akeson, and Daniel Branton. Three decades of nanopore sequencing. In Nature Biotechnology 2016. [16] John J. Kasianowicz, Eric Brandin, Daniel Branton, and David W. Deamer. Characterization of individual polynucleotide molecules using a membrane channel. In Proceedings of the National Academy of Sciences 1996. [17] Amit Meller, Lucas Nivon, Eric Brandin, and others. Rapid nanopore discrimination between single polynucleotide molecules. In Proceedings of the National Academy of Sciences 2000.
[18] David Stoddart, Andrew J. Heron, Ellina Mikhailova, and others. Singlenucleotide discrimination in immobilized DNA oligonucleotides with a biological nanopore. In Proceedings of the National Academy of Sciences 2009. [19] Andrew H. Laszlo, Ian M. Derrington, Henry Brinkerhoff, and others. Detection and mapping of 5-methylcytosine and 5-hydroxymethylcytosine with nanopore MspA. In Proceedings of the National Academy of Sciences 2013. [20] Jacob Schreiber, Zachary L. Wescoe, Robin Abu-Shumays, and others. Error rates for nanopore discrimination among cytosine, methylcytosine, and hydroxymethylcytosine along individual DNA strands. In Proceedings of the National Academy of Sciences 2013. [21] Tom Z. Butler, Mikhail Pavlenok, Ian M. Derrington, and others. Single-molecule DNA detection with an engineered MspA protein nanopore. In Proceedings of the National Academy of Sciences 2008. [22] Ian M. Derrington, Tom Z. Butler, Marcus D. Collins, and others. Nanopore DNA sequencing with MspA. In Proceedings of the National Academy of Sciences 2010. [23] Langzhou Song, Michael R. Hobaugh, Christopher Shustak, and others. Structure of Staphylococcal a-Hemolysin, a Heptameric Transmembrane Pore. In Science 1996. [24] Barbara Walker, John Kasianowicz, Musti Krishnasastry, and Hagan Bayley. A pore-forming protein with a metal-actuated switch. In Protein Engineering, Design and Selection 1994. [25] Zachary L. Wescoe, Jacob Schreiber, and Mark Akeson. Nanopores Discriminate among Five C5-Cytosine Variants in DNA. In Journal of the American Chemical Society 2014. [26] Kate R. Lieberman, Gerald M. Cherf, Michael J. Doody, and others. Processive Replication of Single DNA Molecules in a Nanopore Catalyzed by phi29 DNA Polymerase. In Journal of the American Chemical Society 2010. [27] Sergey M. Bezrukov, Igor Vodyanoy, Rafik A. Brutyan, and John J. Kasianowicz. Dynamics and Free Energy of Polymers Partitioning into a Nanoscale Pore. In Macromolecules 1996. [28] Mark Akeson, Daniel Branton, John J. Kasianowicz, and others. Microsecond Time-Scale Discrimination Among Polycytidylic Acid, Polyadenylic Acid, and Polyuridylic Acid as Homopolymers or as Segments Within Single RNA Molecules. In Biophysical Journal 1999. [29] David Stoddart, Andrew J. Heron, Jochen Klingelhoefer, and others. Nucleobase Recognition in ssDNA at the Central Constriction of the a-Hemolysin Pore. In Nano Letters 2010. [30] Nurit Ashkenasy, Jorge Sánchez-Quesada, Hagan Bayley, and M. Reza Ghadiri. Recognizing a Single Base in an Individual DNA Strand: A Step Toward DNA Sequencing in Nanopores. In Angewandte Chemie International Edition 2005. [31] David Stoddart, Giovanni Maglia, Ellina Mikhailova, and others. Multiple BaseRecognition Sites in a Biological Nanopore: Two Heads are Better than One. In Angewandte Chemie International Edition 2010. [32] Sergey M. Bezrukov and John J. Kasianowicz. Current noise reveals protonation kinetics and number of ionizable sites in an open protein ion channel. In Physical Review Letters 1993. [33] Jia-Yuan Zhang, Yuning Zhang, Lele Wang, and others. A single-molecule nanopore sequencing platform. In bioRxiv 2024. [34] Xiaofeng Dai and Li Shen. Advances and trends in omics technology development. In Frontiers in Medicine 2022. [35] Max Doblas, Po Jui Shih, Oscar Lostes-Cazorla, and others. Smx: Heterogeneous architecture for universal sequence alignment acceleration. In MICRO 2025. [36] Onur Mutlu and Can Firtina. Accelerating Genome Analysis via AlgorithmArchitecture Co-Design. In DAC 2023. [37] Mohammed Alser, Joel Lindegger, Can Firtina, and others. From molecules to genomic variations: Accelerating genome analysis via intelligent algorithms and architectures. In Computational and Structural Biotechnology Journal 2022. [38] Qian Lou, Sarath Chandra Janga, and Lei Jiang. Helix: Algorithm/architecture co-design for accelerating nanopore genome base-calling. In PACT 2020. [39] Qian Lou and Lei Jiang. Brawl: A spintronics-based portable basecalling-inmemory architecture for nanopore genome sequencing. In IEEE CAL 2018. [40] Taha Shahroodi, Gagandeep Singh, Mahdi Zahedi, and others. Swordfish: A Framework for Evaluating Deep Neural Network-based Basecalling using Computation-In-Memory with Non-Ideal Memristors. In MICRO 2023. [41] Ryan Marcus, Andreas Kipf, Alexander van Renen, and others. Benchmarking learned indexes. In PVLDB 2020. [42] Arun Subramaniyan, Jack Wadden, Kush Goliya, and others. Accelerated seeding for genome sequence alignment with enumerated radix trees. In ISCA 2021. [43] Wenqin Huangfu, Shuangchen Li, Xing Hu, and Yuan Xie. RADAR: A 3D-ReRAM based DNA Alignment Accelerator Architecture. In DAC 2018. [44] S Karen Khatamifard, Zamshed Chowdhury, Nakul Pande, and others. GeNVoM: Read Mapping Near Non-Volatile Memory. In IEEE/ACM TCBB 2021. [45] Saransh Gupta, Mohsen Imani, Behnam Khaleghi, and others. RAPID: A ReRAM Processing In-memory Architecture for DNA Sequence Alignment. In ISLPED 2019. [46] Xue-Qi Li, Guang-Ming Tan, and Ning-Hui Sun. PIM-Align: A Processing-inMemory Architecture for FM-Index Search Algorithm. In Journal of Computer
Science and Technology 2021. [47] Shaahin Angizi, Jiao Sun, Wei Zhang, and Deliang Fan. Aligns: A Processing-inmemory Accelerator for DNA Short Read Alignment Leveraging SOT-MRAM. In DAC 2019. [48] Farzaneh Zokaee, Hamid R Zarandi, and Lei Jiang. AligneR: A Process-inmemory Architecture for Short Read Alignment in ReRAMs. In IEEE CAL 2018. [49] Yatish Turakhia, Gill Bejerano, and William J Dally. Darwin: A Genomics Coprocessor Provides up to 15,000 x Acceleration on Long Read Assembly. In ASPLOS 2018. [50] Daichi Fujiki, Arun Subramaniyan, Tianjun Zhang, and others. GenAx: A Genome Sequencing Accelerator. In ISCA 2018. [51] Advait Madhavan, Timothy Sherwood, and Dmitri Strukov. Race Logic: A Hardware Acceleration for Dynamic Programming Algorithms. In ACM SIGARCH Computer Architecture News 2014. [52] Haoyu Cheng, Yong Zhang, and Yun Xu. Bitmapper2: A GPU-accelerated All-mapper Based on The Sparse Q-gram Index. In IEEE/ACM TCBB 2018. [53] Ernst Joachim Houtgast, Vlad-Mihai Sima, Koen Bertels, and Zaid Al-Ars. Hardware Acceleration of BWA-MEM Genomic Short Read Mapping for Longer Read Lengths. In Computational Biology and Chemistry 2018. [54] Ernst Joachim Houtgast, VladMihai Sima, Koen Bertels, and Zaid AlArs. An Efficient GPU-accelerated Implementation of Genomic Short Read Mapping with BWA-MEM. In ACM SIGARCH Computer Architecture News 2017. [55] Alberto Zeni, Giulia Guidi, Marquita Ellis, and others. Logan: High-performance GPU-based X-drop Long-read Alignment. In IPDPS 2020. [56] Nauman Ahmed, Jonathan Lévy, Shanshan Ren, and others. GASAL2: A GPU Accelerated Sequence Alignment Library for High-Throughput NGS Data. In BMC Bioinformatics 2019. [57] Takahiro Nishimura, Jacir L Bordim, Yasuaki Ito, and Koji Nakano. Accelerating the Smith-waterman Algorithm Using Bitwise Parallel Bulk Computation Technique on GPU. In IPDPSW 2017. [58] Edans Flavius de Oliveira Sandes, Guillermo Miranda, Xavier Martorell, and others. CUDAlign 4.0: Incremental Speculative Traceback for Exact Chromosomewide Alignment in GPU Clusters. In IEEE TPDS 2016. [59] Yongchao Liu and Bertil Schmidt. GSWABE: Faster GPU-accelerated Sequence Alignment with Optimal Alignment Retrieval for Short DNA Sequences. In Concurrency and Computation: Practice and Experience 2015. [60] Yongchao Liu, Adrianto Wirawan, and Bertil Schmidt. CUDASW++ 3.0: Accelerating Smith-Waterman Protein Database Search by Coupling CPU and GPU SIMD Instructions. In BMC Bioinformatics 2013. [61] Yongchao Liu, Douglas L Maskell, and Bertil Schmidt. CUDASW++: Optimizing Smith-Waterman Sequence Database Searches for CUDA-enabled Graphics Processing Units. In BMC Research Notes 2009. [62] Yongchao Liu, Bertil Schmidt, and Douglas L Maskell. CUDASW++ 2.0: Enhanced Smith-Waterman Protein Database Search on CUDA-enabled GPUs Based on SIMT and Virtualized SIMD Abstractions. In BMC Research Notes 2010. [63] Richard Wilton, Tamas Budavari, Ben Langmead, and others. Arioc: Highthroughput Read Alignment with GPU-accelerated Exploration of The Seedand-extend Search Space. In PeerJ 2015. [64] Amit Goyal, Hyuk Jung Kwon, Kichan Lee, and others. Ultra-fast Next Generation Human Genome Sequencing Data Processing Using DRAGENTM Bio-IT Processor for Precision Medicine. In Open Journal of Genetics 2017. [65] Yu-Ting Chen, Jason Cong, Zhenman Fang, and others. When Spark Meets FPGAs: A Case Study for Next-Generation DNA Sequencing Acceleration. In USENIX HotCloud 2016. [66] Peng Chen, Chao Wang, Xi Li, and Xuehai Zhou. Accelerating the Next Generation Long Read Mapping with the FPGA-based System. In IEEE/ACM TCBB 2014. [67] Yen-Lung Chen, Bo-Yi Chang, Chia-Hsiang Yang, and Tzi-Dar Chiueh. A HighThroughput FPGA Accelerator for Short-Read Mapping of the Whole Human Genome. In IEEE TPDS 2021. [68] Daichi Fujiki, Shunhao Wu, Nathan Ozog, and others. SeedEx: A Genome Sequencing Accelerator for Optimal Alignments in Subminimal Space. In MICRO 2020. [69] Subho Sankar Banerjee, Mohamed El-Hadedy, Jong Bin Lim, and others. ASAP: Accelerated Short-read Alignment on Programmable Hardware. In IEEE TC 2019. [70] Xia Fei, Zou Dan, Lu Lina, and others. FPGASW: Accelerating Large-scale Smith–Waterman Sequence Alignment Application with Backtracking on FPGA Linear Systolic Array. In Interdisciplinary Sciences: Computational Life Sciences 2018. [71] Hasitha Muthumala Waidyasooriya and Masanori Hariyama. Hardwareacceleration of Short-read Alignment Based on the Burrows-wheeler Transform. In IEEE TPDS 2015. [72] Yu-Ting Chen, Jason Cong, Jie Lei, and Peng Wei. A Novel High-throughput Acceleration Engine for Read Alignment. In FCCM 2015.
[73] Enzo Rucci, Carlos Garcia, Guillermo Botella, and others. SWIFOLD: SmithWaterman Implementation on FPGA with OpenCL for Long DNA Sequences. In BMC Systems Biology 2018. [74] Abbas Haghi, Santiago Marco-Sola, Lluc Alvarez, and others. An FPGA Accelerator of the Wavefront Algorithm for Genomics Pairwise Alignment. In FPL 2021. [75] Luyi Li, Jun Lin, and Zhongfeng Wang. PipeBSW: A Two-Stage Pipeline Structure for Banded Smith-Waterman Algorithm on FPGA. In ISVLSI 2021. [76] Tae Jun Ham, David Bruns-Smith, Brendan Sweeney, and others. Genesis: A Hardware Acceleration Framework for Genomic Data Analysis. In ISCA 2020. [77] Tae Jun Ham, Yejin Lee, Seong Hoon Seo, and others. Accelerating Genomic Data Analytics With Composable Hardware Acceleration Framework. In IEEE Micro 2021. [78] Lisa Wu, David Bruns-Smith, Frank A. Nothaft, and others. FPGA Accelerated Indel Realignment in the Cloud. In HPCA 2019. [79] Damla Senol Cali, Gurpreet S. Kalsi, Zülal Bingöl, and others. GenASM: A High-Performance, Low-Power Approximate String Matching Acceleration Framework for Genome Sequence Analysis. In MICRO 2020. [80] Fan Zhang, Shaahin Angizi, Jiao Sun, and others. Aligner-D: Leveraging InDRAM Computing to Accelerate DNA Short Read Alignment. In IEEE JETCAS 2023. [81] Melina Soysal, Konstantina Koliogeorgi, Can Firtina, and others. MARS: Processing-in-memory acceleration of raw signal genome analysis inside the storage subsystem. In ICS 2025. [82] Jeremie S Kim, Damla Senol Cali, Hongyi Xin, and others. GRIM-Filter: Fast Seed Location Filtering in DNA Read Mapping Using Processing-in-memory Technologies. In BMC Genomics 2018. [83] Roman Kaplan, Leonid Yavits, and Ran Ginosasr. BioSEAL: In-memory biological sequence alignment accelerator for large-scale genomic data. In SYSTOR 2020. [84] Haiyu Mao, Mohammed Alser, Mohammad Sadrosadati, and others. GenPIP: InMemory Acceleration of Genome Analysis via Tight Integration of Basecalling and Read Mapping. In MICRO 2022. [85] Yingqi Cao, Anshu Guta, Jason Liang, and Yatish Turakhia. DP-HLS: A HighLevel Synthesis Framework for Accelerating Dynamic Programming Algorithms in Bioinformatics. In HPCA 2026. [86] Zhehong Wang, Tianjun Zhang, Daichi Fujiki, and others. A 2.46 M Reads/s seed-extension accelerator for next-generation sequencing using a stringindependent PE array. In IEEE JSSC 2020. [87] Sumit Walia, Cheng Ye, Arkid Bera, and others. TALCO: Tiling Genome Sequence Alignment Using Convergence of Traceback Pointers. In HPCA 2024. [88] Harisankar Sadasivan, Artur Klauser, Juergen Hench, and others. The Genomic Computing Revolution: Defining the Next Decades of Accelerating Genomics. In HPEC 2024. [89] Yatish Turakhia. Toward a Generalized Accelerator for Genome Sequence Analysis. In Commun. ACM 2025. [90] Yatish Turakhia, Sneha D. Goenka, Gill Bejerano, and WIlliam J. Dally. DarwinWGA: A Co-processor Provides Increased Sensitivity in Whole Genome Alignments with High Speedup. In HPCA 2019. [91] William Andrew Simon, Leonid Yavits, Konstantina Koliogeorgi, and others. Processing-in-memory for genomics workloads. In IEEE Micro 2026. [92] Julien Eudine, Chu Li, Zhuo Cheng, and others. GenPairX: A HardwareAlgorithm Co-Designed Accelerator for Paired-End Read Mapping. In HPCA 2026. [93] Joël Lindegger, Damla Senol Cali, Mohammed Alser, and others. Scrooge: a fast and memory-frugal genomic sequence aligner for CPUs, GPUs, and ASICs. In Bioinformatics 2023. [94] Zheng Zhang, Scott Schwartz, Lukas Wagner, and Webb Miller. A Greedy Algorithm for Aligning DNA Sequences. In Journal of Computational Biology 2000. [95] Guy St C Slater and Ewan Birney. Automated Generation of Heuristics for Biological Sequence Comparison. In BMC Bioinformatics 2005. [96] Heng Li. Minimap2: Pairwise Alignment for Nucleotide Sequences. In Bioinformatics 2018. [97] Gene Myers. A Fast Bit-vector Algorithm for Approximate String Matching Based on Dynamic Programming. In JACM 1999. [98] Santiago Marco-Sola, Juan Carlos Moure, Miquel Moreto, and Antonio Espinosa. Fast Gap-affine Pairwise Alignment Using the Wavefront Algorithm. In Bioinformatics 2021. [99] Santiago Marco-Sola, Jordan M Eizenga, Andrea Guarracino, and others. Optimal gap-affine alignment in O(s) space. In Bioinformatics 2023. [100] Ragnar Groot Koerkamp. A*PA2: Up to 19× Faster Exact Global Alignment. In WABI 2024. [101] Hongyi Xin, Donghyuk Lee, Farhad Hormozdiari, and others. Accelerating Read Mapping with FastHASH. In BMC Genomics 2013. [102] Hongyi Xin, John Greth, John Emmons, and others. Shifted Hamming Distance: A Fast and Accurate SIMD-friendly Filter to Accelerate Alignment Verification in Read Mapping. In Bioinformatics 2015.
[103] Yu-Hsiang Tseng, Sumit Walia, and Yatish Turakhia. Ultrafast and ultralarge multiple sequence alignments using TWILIGHT. In Bioinformatics 2025. [104] Sumit Walia, Zexing Chen, Yu-Hsiang Tseng, and Yatish Turakhia. Ultrafast and Ultralarge Distance-Based Phylogenetics Using DIPPER. In bioRxiv 2025. [105] Jeremie S Kim, Can Firtina, Meryem Banu Cavlak, and others. FastRemap: a tool for quickly remapping reads between genome assemblies. In Bioinformatics 2022. [106] Akmuhammet Ashyralyyev, Ege Sirvan, Ecem İlgün, and others. GenCore: Genomic distance estimation using Locally Consistent Parsing. In bioRxiv 2026. [107] Akmuhammet Ashyralyyev, Zülal Bingöl, Begüm Filiz Öz, and others. LCPan: efficient variation graph construction using Locally Consistent Parsing. In arXiv 2026. [108] Ahmet Cemal Alıcıoğlu and Can Alkan. Pairwise sequence alignment with block and character edit operations. In arXiv 2024. [109] Udi Manber and Gene Myers. Suffix arrays: a new method for on-line string searches. In Siam Journal on Computing 1993. [110] Zhong Wang, Mark Gerstein, and Michael Snyder. RNA-Seq: a revolutionary tool for transcriptomics. In Nature Reviews Genetics 2009. [111] Rohan Lowe, Neil Shirley, Mark Bleackley, and others. Transcriptomics technologies. In PLOS Computational Biology 2017. [112] Philipp Angerer, Lukas Simon, Sophie Tritschler, and others. Single cells make big data: New challenges and opportunities in transcriptomics. In Current Opinion in Systems Biology 2017. [113] Rory Stark, Marta Grzelak, and James Hadfield. RNA sequencing: the teenage years. In Nature Reviews Genetics 2019. [114] Jiung-Wen Chen, Lisa Shrestha, George Green, and others. The hitchhikers’ guide to RNA sequencing and functional analysis. In Briefings in Bioinformatics 2023. [115] Jason L Weirather, Mariateresa de Cesare, Yunhao Wang, and others. Comprehensive Comparison of Pacific Biosciences and Oxford Nanopore Technologies and Their Applications to Transcriptome Analysis. In F1000Research 2017. [116] Jonas A. Sibbesen, Jordan M. Eizenga, Adam M. Novak, and others. Haplotypeaware pantranscriptome analyses using spliced pangenome graphs. In Nature Methods 2023. [117] Cordula Haas, Jacqueline Neubauer, Andrea Patrizia Salzmann, and others. Forensic transcriptome analysis using massively parallel sequencing. In Forensic Science International: Genetics 2021. [118] Bo Liu, Yadong Liu, Junyi Li, and others. deSALT: fast and accurate long transcriptomic read alignment with de Bruijn graph-based index. In Genome Biology 2019. [119] Alexander Lachmann, Denis Torre, Alexandra B. Keenan, and others. Massive mining of publicly available RNA-seq data from human and mouse. In Nature Communications 2018. [120] Emily Clough, Tanya Barrett, Stephen E Wilhite, and others. NCBI GEO: archive for gene expression and epigenomics data sets: 23-year update. In Nucleic Acids Research 2023. [121] Nicolas L Bray, Harold Pimentel, Páll Melsted, and Lior Pachter. Near-optimal probabilistic RNA-seq quantification. In Nature Biotechnology 2016. [122] Parag Mallick and Bernhard Kuster. Proteomics: a pragmatic perspective. In Nature Biotechnology 2010. [123] Bilal Aslam, Madiha Basit, Muhammad Atif Nisar, and others. Proteomics: technologies and their applications. In Journal of Chromatographic Science 2016. [124] William CS Cho. Proteomics technologies and challenges. In Genomics, Proteomics & Bioinformatics 2007. [125] Scott D Patterson and Ruedi H Aebersold. Proteomics: the first decade and beyond. In Nature Genetics 2003. [126] Paul R Graves and Timothy AJ Haystead. Molecular biologist’s guide to proteomics. In Microbiology and Molecular Biology Reviews 2002. [127] Akhilesh Pandey and Matthias Mann. Proteomics to study genes and genomes. In Nature 2000. [128] Saleh Alseekh et al. Mass spectrometry-based metabolomics: a guide for annotation, quantification and best reporting practices. In Nature Methods 2021. [129] Yasset Perez-Riverol et al. Quantifying the impact of public omics data. In Nature Communications 2019. [130] Xiaojing Liu and Jason W Locasale. Metabolomics: a primer. In Trends in Biochemical Sciences 2017. [131] Aihua Zhang, Hui Sun, Ping Wang, and others. Modern analytical techniques in metabolomics analysis. In Analyst 2012. [132] Caroline H Johnson and Frank J Gonzalez. Challenges and opportunities of metabolomics. In Journal of Cellular Physiology 2012. [133] Luis Martí-Bonmatí, Ramón Sopena, Paula Bartumeus, and Pablo Sopena. Multimodality imaging techniques. In Contrast Media & Molecular Imaging 2010. [134] Hany Kasban et al. A comparative study of medical imaging techniques. In International Journal of Information Science and Intelligent System 2015. [135] K Kirk Shung, Michael Smith, and Benjamin MW Tsui. 2012. Principles of Medical Imaging.
[136] Gary H Glover. Overview of functional magnetic resonance imaging. In Neurosurgery Clinics of North America 2011. [137] Vibhu Kapoor, Barry M McCook, and Frank S Torok. An introduction to PET-CT imaging. In Radiographics 2004. [138] DW Townsend et al. Physical principles and technology of clinical PET imaging. In Annals-Academy of Medicine Singapore 2004. [139] Changhyun Pang, Chanseok Lee, and Kahp-Yang Suh. Recent advances in flexible sensors for wearable and implantable devices. In Journal of Applied Polymer Science 2013. [140] Hatice Ceylan Koydemir and Aydogan Ozcan. Wearable and implantable sensors for biomedical applications. In Annual Review of Analytical Chemistry 2018. [141] Marie Chan, Daniel Estève, Jean-Yves Fourniols, and others. Smart wearable systems: Current status and future challenges. In Artificial Intelligence in Medicine 2012. [142] Paul Lukowicz, Tnde Kirstein, and Gerhard Tröster. Wearable systems for health care applications. In Methods of Information in Medicine 2004. [143] Paolo Bonato. Wearable sensors and systems. In IEMBDE 2010. [144] Michelle M. Clark, Amber Hildreth, Sergey Batalov, and others. Diagnosis of Genetic Diseases in Seriously Ill Children by Rapid Whole-genome Sequencing and Automated Phenotyping and Interpretation. In Science Translational Medicine 2019. [145] Lauge Farnaes, Amber Hildreth, Nathaly M. Sweeney, and others. Rapid Wholegenome Sequencing Decreases Infant Morbidity and Cost of Hospitalization. In NPJ Genomic Medicine 2018. [146] Nathaly M. Sweeney, Shareef A. Nahas, Shimul Chowdhury, and others. Rapid Whole Genome Sequencing Impacts Care and Resource Utilization in Infants with Congenital Heart Disease. In NPJ Genomic Medicine 2021. [147] Can Alkan, Jeffrey M Kidd, Tomas Marques-Bonet, and others. Personalized Copy Number and Segmental Duplication Maps Using Next-Generation Sequencing. In Nature Genetics 2009. [148] Mauricio Flores, Gustavo Glusman, Kristin Brogaard, and others. P4 Medicine: How Systems Medicine Will Transform the Healthcare Sector and Society. In Personalized Medicine 2013. [149] Geoffrey S Ginsburg and Huntington F Willard. Genomic and Personalized Medicine: Foundations and Applications. In Translational Research 2009. [150] Lynda Chin, Jannik N Andersen, and P Andrew Futreal. Cancer Genomics: From Discovery Science to Personalized Medicine. In Nature Medicine 2011. [151] Euan A Ashley. Towards Precision Medicine. In Nature Reviews Genetics 2016. [152] Can Alkan, Jeffrey M Kidd, Tomas Marques-Bonet, and others. Personalized copy number and segmental duplication maps using next-generation sequencing. In Nature Genetics 2009. [153] Gaye Lightbody, Valeriia Haberland, Fiona Browne, and others. Review of applications of high-throughput sequencing in personalized medicine: barriers and facilitators of future progress in research and clinical application. In Briefings in Bioinformatics 2019. [154] Stefania Morganti, Paolo Tarantino, Emanuela Ferraro, and others. Next Generation Sequencing (NGS): A Revolutionary Technology in Pharmacogenomics and Personalized Medicine in Cancer. In Translational Research and Onco-Omics Applications in the Era of Cancer Personal Genomics. 2019. [155] Iuliia Branco and Altino Choupina. Bioinformatics: new tools and applications in life science and personalized medicine. In Applied Microbiology and Biotechnology 2021. [156] Sameer Quazi. Artificial intelligence and machine learning in precision and genomic medicine. In Medical Oncology 2022. [157] Samuel J. Aronson and Heidi L. Rehm. Building the foundation for genomics in precision medicine. In Nature 2015. [158] Hannah F. Löchel and Dominik Heider. Comparative analyses of error handling strategies for next-generation sequencing in precision medicine. In Scientific Reports 2020. [159] Eirini Papadopoulou, Dimitra Bouzarelou, George Tsaousis, and others. Application of next generation sequencing in cardiology: current and future precision medicine implications. In Frontiers in Cardiovascular Medicine 2023. [160] Alireza Tafazoli, Henk-Jan Guchelaar, Wojciech Miltyk, and others. Applying Next-Generation Sequencing Platforms for Pharmacogenomic Testing in Clinical Practice. In Frontiers in Pharmacology 2021. [161] Valentina Gambardella, Noelia Tarazona, Juan M. Cejalvo, and others. Personalized Medicine: Recent Progress in Cancer Therapy. In Cancers 2020. [162] Rebecca J. Leary, Isaac Kinde, Frank Diehl, and others. Development of Personalized Tumor Biomarkers Using Massively Parallel Sequencing. In Science Translational Medicine 2010. [163] Hamburg Margaret A. and Collins Francis S. The Path to Personalized Medicine. In New England Journal of Medicine 2010. [164] Maaike van der Lee, Marjolein Kriek, Henk-Jan Guchelaar, and Jesse J. Swen. Technologies for Pharmacogenomics: A Review. In Genes 2020. [165] Dabin Moon, Hye W. Park, Dongheon Surl, and others. Precision Medicine through Next-Generation Sequencing in Inherited Eye Diseases in a Korean Cohort. In Genes 2022.
[166] Sumitra Mohan, Victoria Foy, Mahmood Ayub, and others. Profiling of Circulating Free DNA Using Targeted and Genome-wide Sequencing in Patients with SCLC. In Journal of Thoracic Oncology 2020. [167] Claudia C.Y. Chung, Gordon K.C. Leung, Christopher C.Y. Mak, and others. Rapid whole-exome sequencing facilitates precision medicine in paediatric rare disease patients and reduces healthcare costs. In The Lancet Regional Health – Western Pacific 2020. [168] Suzette J. Bielinski, Janet E. Olson, Jyotishman Pathak, and others. Preemptive Genotyping for Personalized Medicine: Design of the Right Drug, Right Dose, Right Time—Using Genomic Data to Individualize Treatment Protocol. In Mayo Clinic Proceedings 2014. [169] Dean Ho, Stephen R. Quake, Edward R.B. McCabe, and others. Enabling Technologies for Personalized and Precision Medicine. In Trends in Biotechnology 2020. [170] Bashdar Mahmud Hussen, Sara Tharwat Abdullah, Abbas Salihi, and others. The emerging roles of NGS in clinical oncology and personalized medicine. In Pathology - Research and Practice 2022. [171] Laura E. Russell, Yitian Zhou, Ahmed A. Almousa, and others. Pharmacogenomics in the era of next generation sequencing – from byte to bedside. In Drug Metabolism Reviews 2021. [172] Renu Verma, Kesia Esther da Silva, Neesha Rockwood, and others. A Nanopore Sequencing-based Pharmacogenomic Panel to Personalize Tuberculosis Drug Dosing. In American Journal of Respiratory and Critical Care Medicine 2024. [173] Tim Dunn, Harisankar Sadasivan, Jack Wadden, and others. SquiggleFilter: An accelerator for portable virus detection. In MICRO 2021. [174] C. Bertelli and G. Greub. Rapid bacterial genome sequencing: methods and applications in clinical microbiology. In Clinical Microbiology and Infection 2013. [175] Armando Arias, Simon J. Watson, Danny Asogun, and others. Rapid outbreak sequencing of Ebola virus in Sierra Leone identifies transmission chains linked to sporadic cases. In Virus Evolution 2016. [176] Jessica Comin, Armando Chaure, Alberto Cebollada, and others. Investigation of a rapidly spreading tuberculosis outbreak using whole-genome sequencing. In Infection, Genetics and Evolution 2020. [177] Joshua Quick, Nicholas J. Loman, Sophie Duraffour, and others. Real-time, portable genome sequencing for Ebola surveillance. In Nature 2016. [178] Esther R. Robinson, Timothy M. Walker, and Mark J. Pallen. Genomics and outbreak investigation: from sequence to consequence. In Genome Medicine 2013. [179] Pierre-Edouard Fournier, Gregory Dubourg, and Didier Raoult. Clinical detection and characterization of bacterial pathogens in the genomics era. In Genome Medicine 2014. [180] Claudio U. Köser, Matthew J. Ellington, Edward J. P. Cartwright, and others. Routine Use of Microbial Whole Genome Sequencing in Diagnostic and Public Health Microbiology. In PLOS Pathogens 2012. [181] Marc Eloit and marc lecuit. The diagnosis of infectious diseases by whole genome next generation sequencing: a new era is opening. In Frontiers in Cellular and Infection Microbiology 2014. [182] Gardy Jennifer L., Johnston James C., Sui Shannan J. Ho, and others. WholeGenome Sequencing and Social-Network Analysis of a Tuberculosis Outbreak. In New England Journal of Medicine 2011. [183] Taylor Angela J., Lappi Victoria, Wolfgang William J., and others. Characterization of Foodborne Outbreaks of Salmonella enterica Serovar Enteritidis with Whole-Genome Sequencing Single Nucleotide Polymorphism-Based Analysis for Surveillance and Outbreak Detection. In Journal of Clinical Microbiology 2015. [184] Quainoo Scott, Coolen Jordy P. M., van Hijum Sacha A. F. T., and others. WholeGenome Sequencing of Bacterial Pathogens: the Future of Nosocomial Outbreak Analysis. In Clinical Microbiology Reviews 2017. [185] Goldberg Brittany, Sichtig Heike, Geyer Chelsie, and others. Making the Leap from Research Laboratory to Clinic: Challenges and Opportunities for NextGeneration Sequencing in Infectious Disease Diagnostics. In mBio 2015. [186] John M. Besser, Heather A. Carleton, Eija Trees, and others. Interpretation of Whole-Genome Sequencing for Enteric Disease Surveillance and Outbreak Investigation. In Foodborne Pathogens and Disease 2019. [187] Weiwei Li, Qingpo Cui, Li Bai, and others. Application of Whole-Genome Sequencing in the National Molecular Tracing Network for Foodborne Disease Surveillance in China. In Foodborne Pathogens and Disease 2021. [188] Yinhua Deng, Min Jiang, Patrick S.L. Kwan, and others. Integrated WholeGenome Sequencing Infrastructure for Outbreak Detection and Source Tracing of Salmonella enterica Serotype Enteritidis. In Foodborne Pathogens and Disease 2021. [189] J.C. Kwong, N. Mccallum, V. Sintchenko, and B.P. Howden. Whole genome sequencing in clinical and public health microbiology. In Pathology 2015. [190] Ruud H. Deurenberg, Erik Bathoorn, Monika A. Chlebowicz, and others. Application of next generation sequencing in clinical microbiology and infection prevention. In Journal of Biotechnology 2017.
[191] Patrick Tang, Matthew A. Croxen, Mohammad R. Hasan, and others. Infection control in the new age of genomic epidemiology. In American Journal of Infection Control 2017. [192] Nicholas J Croucher and Xavier Didelot. The application of genomics to tracing bacterial pathogen transmission. In Host–microbe interactions: bacteria • Genomics 2015. [193] Joshua S. Bloom, Laila Sathe, Chetan Munugala, and others. Massively Scaled-up Testing for SARS-CoV-2 RNA via Next-generation Sequencing of Pooled and Barcoded Nasal and Saliva Samples. In Nature Biomedical Engineering 2021. [194] Ramesh Yelagandula, Aleksandr Bykov, Alexander Vogt, and others. Multiplexed Detection of SARS-CoV-2 and Other Respiratory Infections in High Throughput by SARSeq. In Nature Communications 2021. [195] Vien Thi Minh Le and Binh An Diep. Selected Insights from Application of Whole Genome Sequencing for Outbreak Investigations. In Current Opinion in Critical Care 2013. [196] Vlad Nikolayevskyy, Katharina Kranzer, Stefan Niemann, and Francis Drobniewski. Whole Genome Sequencing of Mycobacterium Tuberculosis for Detection of Recent Transmission and Tracing Outbreaks: A Systematic Review. In Tuberculosis 2016. [197] Shaofu Qiu, Peng Li, Hongbo Liu, and others. Whole-genome Sequencing for Tracing the Transmission Link between Two ARD Outbreaks Caused by A Novel HAdV Serotype 7 Variant, China. In Scientific Reports 2015. [198] Carol A Gilchrist, Stephen D Turner, Margaret F Riley, and others. Wholegenome Sequencing in Outbreak Analysis. In Clinical Microbiology Reviews 2015. [199] Michael S. Lawrence, Petar Stojanov, Paz Polak, and others. Mutational heterogeneity in cancer and the search for new cancer-associated genes. In Nature 2013. [200] Bert Vogelstein, Nickolas Papadopoulos, Victor E. Velculescu, and others. Cancer Genome Landscapes. In Science 2013. [201] Daniel Ramsköld, Shujun Luo, Yu-Chieh Wang, and others. Full-length mRNASeq from single-cell levels of RNA and individual circulating tumor cells. In Nature Biotechnology 2012. [202] Timour Baslan and James Hicks. Unravelling biology and shifting paradigms in cancer with single-cell sequencing. In Nature Reviews Cancer 2017. [203] Ehud Shapiro, Tamir Biezuner, and Sten Linnarsson. Single-cell sequencingbased technologies will revolutionize whole-organism science. In Nature Reviews Genetics 2013. [204] Yoshitaka Sakamoto, Sarun Sereewattanawoot, and Ayako Suzuki. A new era of long-read sequencing for cancer genomics. In Journal of Human Genetics 2020. [205] Qingzhu Jia, Han Chu, Zheng Jin, and others. High-throughput single-cell sequencing in cancer research. In Signal Transduction and Targeted Therapy 2022. [206] Devon A. Lawson, Kai Kessenbrock, Ryan T. Davis, and others. Tumour heterogeneity and metastasis at single-cell resolution. In Nature Cell Biology 2018. [207] Chuang Liu, Qiangqiang Shi, Xiangang Huang, and others. mRNA-based cancer therapeutics. In Nature Reviews Cancer 2023. [208] Bram Van de Sande, Joon Sang Lee, Euphemia Mutasa-Gottgens, and others. Applications of single-cell RNA sequencing in drug discovery and development. In Nature Reviews Drug Discovery 2023. [209] Debyani Chakravarty and David B. Solit. Clinical cancer genomic profiling. In Nature Reviews Genetics 2021. [210] Isidro Cortés-Ciriano, Doga C. Gulhan, Jake June-Koo Lee, and others. Computational analysis of cancer genome sequencing data. In Nature Reviews Genetics 2022. [211] Ira W. Deveson, Binsheng Gong, Kevin Lai, and others. Evaluating the analytical validity of circulating tumor DNA sequencing assays for precision oncology. In Nature Biotechnology 2021. [212] Wenming Xiao, Luyao Ren, Zhong Chen, and others. Toward best practice in cancer mutation detection with whole-genome and whole-exome sequencing. In Nature Biotechnology 2021. [213] Kelly L. Bolton, Ryan N. Ptashkin, Teng Gao, and others. Cancer therapy shapes the fitness landscape of clonal hematopoiesis. In Nature Genetics 2020. [214] Joseph D. Szustakowski, Suganthi Balasubramanian, Erika Kvikstad, and others. Advancing human genetics research and drug discovery through exome sequencing of the UK Biobank. In Nature Genetics 2021. [215] Nicholas Navin and James Hicks. Future medical applications of single-cell sequencing in cancer. In Genome Medicine 2011. [216] Mingye Hong, Shuang Tao, Ling Zhang, and others. RNA sequencing: new technologies and applications in cancer research. In Journal of Hematology & Oncology 2020. [217] Yalan Lei, Rong Tang, Jin Xu, and others. Applications of single-cell sequencing in cancer research: progress and perspectives. In Journal of Hematology & Oncology 2021. [218] Yingying Han, Dan Wang, Lushan Peng, and others. Single-cell sequencing: a promising approach for uncovering the mechanisms of tumor metastasis. In Journal of Hematology & Oncology 2022.
[219] Giulia Federici and Silvia Soddu. Variants of uncertain significance in the era of high-throughput genome sequencing: a lesson from breast and ovary cancers. In Journal of Experimental & Clinical Cancer Research 2020. [220] Yijie Zhang, Dan Wang, Miao Peng, and others. Single-cell RNA sequencing in cancer research. In Journal of Experimental & Clinical Cancer Research 2021. [221] Xianwen Ren, Boxi Kang, and Zemin Zhang. Understanding tumor ecosystems by single-cell sequencing: promises and limitations. In Genome Biology 2018. [222] Liqing Tian, Yongjin Li, Michael N. Edmonson, and others. CICERO: a versatile method for detecting complex and diverse driver fusions using cancer RNA sequencing data. In Genome Biology 2020. [223] Eoghan R. Malone, Marc Oliva, Peter J. B. Sabatini, and others. Molecular profiling for precision cancer therapies. In Genome Medicine 2020. [224] Xiaoning Tang, Yongmei Huang, Jinli Lei, and others. The single-cell sequencing: new developments and medical applications. In Cell & Bioscience 2019. [225] Darrell L. Ellsworth, Heather L. Blackburn, Craig D. Shriver, and others. Singlecell sequencing and tumorigenesis: improved understanding of tumor evolution and metastasis. In Clinical and Translational Medicine 2017. [226] Yiming Zhong, Feng Xu, Jinhua Wu, and others. Application of Next Generation Sequencing in Laboratory Medicine. In Annals of Laboratory Medicine 2021. [227] Zsofia K. Stadler, Anna Maio, Debyani Chakravarty, and others. Therapeutic Implications of Germline Testing in Patients With Advanced Cancers. In Journal of Clinical Oncology 2021. [228] Aaron C. Tan and Daniel S.W. Tan. Targeted Therapies for Lung Cancer Patients With Oncogenic Driver Molecular Alterations. In Journal of Clinical Oncology 2022. [229] Andrea Degasperi, Xueqing Zou, Tauanne Dias Amarante, and others. Substitution mutational signatures in whole-genome–sequenced cancers in the UK population. In Science 2022. [230] Junfen Xu, Yifeng Fang, Kelie Chen, and others. Single-Cell RNA Sequencing Reveals the Tissue Architecture in Human High-Grade Serous Ovarian Cancer. In Clinical Cancer Research 2022. [231] Peter Horak, Christoph Heining, Simon Kreutzfeldt, and others. Comprehensive Genomic and Transcriptomic Analysis for Guiding Therapeutic Decisions in Patients with Rare Cancers. In Cancer Discovery 2021. [232] Xiaoyan Zhang, Sadie L. Marjani, Zhaoyang Hu, and others. Single-Cell Sequencing for Precise Cancer Research: Progress and Prospects. In Cancer Research 2016. [233] Rossella Bruno and Gabriella Fontanini. Next Generation Sequencing for Gene Fusion Analysis in Lung Cancer: A Literature Review. In Diagnostics 2020. [234] Antonella De Luca, Riziero Esposito Abate, Anna M. Rachiglio, and others. FGFR Fusions in Cancer: From Diagnostic Approaches to Therapeutic Intervention. In International Journal of Molecular Sciences 2020. [235] Michael R. Waarts, Aaron J. Stonestrom, Young C. Park, and Ross L. Levine. Targeting mutations in cancer. In The Journal of Clinical Investigation 2022. [236] Bora Lim, Yiyun Lin, and Nicholas Navin. Advancing Cancer Research and Medicine with Single-Cell Genomics. In Cancer Cell 2020. [237] Ramon Colomer, Rebeca Mondejar, Nuria Romero-Laorden, and others. When should we order a next generation sequencing test in a patient with cancer? In eClinicalMedicine 2020. [238] Assieh Saadatpour, Shujing Lai, Guoji Guo, and Guo-Cheng Yuan. Single-Cell Analysis in Cancer Genomics. In Trends in Genetics 2015. [239] Nazli Dizman, Zeynep E. Arslan, Matthew Feng, and Sumanta K. Pal. Sequencing Therapies for Metastatic Renal Cell Carcinoma. In Urologic Clinics 2020. [240] Anton Buzdin, Maxim Sorokin, Andrew Garazha, and others. RNA sequencing for research and diagnostics in clinical oncology. In Seminars in Cancer Biology 2020. [241] Yi Xiao and Dihua Yu. Tumor microenvironment as a therapeutic target in cancer. In Pharmacology & Therapeutics 2021. [242] Arun Nandwani, Shalu Rathore, and Malabika Datta. LncRNAs in cancer: Regulatory and therapeutic implications. In Cancer Letters 2021. [243] Francesco Marchetti, Renato Cardoso, Connie L. Chen, and others. Errorcorrected next generation sequencing – Promises and challenges for genotoxicity and cancer risk assessment. In Mutation Research/Reviews in Mutation Research 2023. [244] Xiao Chen, Han Zhu, Chun Qiao, and others. Next-generation sequencing reveals gene mutations landscape and clonal evolution in patients with acute myeloid leukemia. In Hematology 2021. [245] Nicholas E. Navin. The first five years of single-cell cancer genomics and beyond. In Genome Research 2015. [246] Augusto Dulanto Chiang and John P Dekker. From the Pipeline to the Bedside: Advances and Challenges in Clinical Metagenomics. In The Journal of Infectious Diseases 2019. [247] The Arabidopsis Genome Initiative. Analysis of the genome sequence of the flowering plant Arabidopsis thaliana. In Nature 2000. [248] Haocheng Zhu, Chao Li, and Caixia Gao. Applications of CRISPR–Cas in agriculture and plant biotechnology. In Nature Reviews Molecular Cell Biology 2020.
[249] Jae Young Choi, Zoe N. Lye, Simon C. Groen, and others. Nanopore sequencingbased genome assembly and evolutionary genomics of circum-basmati rice. In Genome Biology 2020. [250] Kristian A Stevens, Jill L Wegrzyn, Aleksey Zimin, and others. Sequence of the Sugar Pine Megagenome. In Genetics 2016. [251] Maria Doroteia Campos, Maria do Rosário Félix, Mariana Patanita, and others. High throughput sequencing unravels tomato-pathogen interactions towards a sustainable plant breeding. In Horticulture Research 2021. [252] Caixia Gao. Genome engineering for crop improvement and future agriculture. In Cell 2021. [253] Aalt Dirk Jan van Dijk, Gert Kootstra, Willem Kruijer, and Dick de Ridder. Machine learning in plant science and plant breeding. In iScience 2021. [254] Yanqing Sun, Lianguang Shang, Qian-Hao Zhu, and others. Twenty years of plant genome sequencing: achievements and challenges. In Trends in Plant Science 2022. [255] Kyung D. Kim, Yuna Kang, and Changsoo Kim. Application of Genomic Big Data in Plant Breeding: Past, Present, and Future. In Plants 2020. [256] Mahendar Thudi, Ramesh Palakurthi, James C. Schnable, and others. Genomic resources in plant breeding for sustainable agriculture. In Journal of Plant Physiology 2021. [257] Todd P Michael and Robert VanBuren. Building near-complete plant genomes. In Current Opinion in Plant Biology 2020. [258] Yanting Shen, Guoan Zhou, Chengzhi Liang, and Zhixi Tian. Omics-based interdisciplinarity is accelerating plant breeding. In Current Opinion in Plant Biology 2022. [259] Taha Shahroodi, Mahdi Zahedi, Can Firtina, and others. Demeter: A fast and energy-efficient food profiler using hyperdimensional computing in memory. In IEEE Access 2022. [260] Shiv Prasad, Lal Chand Malav, Jairam Choudhary, and others. Soil Microbiomes for Healthy Nutrient Recycling. In Current Trends in Microbial Biotechnology for Sustainable Agriculture 2021. [261] Martin Mascher, Murukarthick Jayakodi, Hyeonah Shim, and Nils Stein. Promises and challenges of crop translational genomics. In Nature 2024. [262] Mona Schreiber, Murukarthick Jayakodi, Nils Stein, and Martin Mascher. Plant pangenomes for crop improvement, biodiversity and evolution. In Nature Reviews Genetics 2024. [263] NIHR Global Health Research Unit on Genomic Surveillance of AMR. Wholegenome sequencing as part of national and international surveillance programmes for antimicrobial resistance: a roadmap. In BMJ Global Health 2020. [264] Shanwei Tong, Luyao Ma, Jennifer Ronholm, and others. Whole genome sequencing of Campylobacter in agri-food surveillance. In Current Opinion in Food Science 2021. [265] Aneta K. Urbanek, Waldemar Rymowicz, and Aleksandra M. Mirończuk. Degradation of plastics and plastic-degrading bacteria in cold marine habitats. In Applied Microbiology and Biotechnology 2018. [266] Robert C. Edgar, Jeff Taylor, Victor Lin, and others. Petabase-scale sequence alignment catalyses viral discovery. In Nature 2022. [267] Lucas Paoli, Hans-Joachim Ruscheweyh, Clarissa C. Forneris, and others. Biosynthetic potential of the global ocean microbiome. In Nature 2022. [268] Carolyn J. Hogg. Translating genomic advances into biodiversity conservation. In Nature Reviews Genetics 2024. [269] Harris A. Lewin, Gene E. Robinson, W. John Kress, and others. Earth BioGenome Project: Sequencing life for the future of life. In Proceedings of the National Academy of Sciences 2018. [270] Minoru Kanehisa. Toward understanding the origin and evolution of cellular organisms. In Protein Science 2019. [271] Jun Qing, Yi-De Meng, Feng He, and others. Whole genome re-sequencing reveals the genetic diversity and evolutionary patterns of Eucommia ulmoides. In Molecular Genetics and Genomics 2022. [272] Patricia J. Wittkopp and Gizem Kalay. Cis-regulatory elements: molecular mechanisms and evolutionary processes underlying divergence. In Nature Reviews Genetics 2012. [273] Irene Gallego Romero, Ilya Ruvinsky, and Yoav Gilad. Comparative studies of gene expression and the evolution of gene regulation. In Nature Reviews Genetics 2012. [274] Xinchao Wang, Hu Feng, Yuxiao Chang, and others. Population sequencing enhances understanding of tea plant evolution. In Nature Communications 2020. [275] Mark S. Hill, Pétra Vande Zande, and Patricia J. Wittkopp. Molecular and evolutionary processes generating variation in gene expression. In Nature Reviews Genetics 2021. [276] Eeshit Dhaval Vaishnav, Carl G. de Boer, Jennifer Molinet, and others. The evolution, evolvability and engineering of gene regulatory DNA. In Nature 2022. [277] Xingtan Zhang, Shuai Chen, Longqing Shi, and others. Haplotype-resolved genome assembly provides insights into evolutionary history of the tea plant Camellia sinensis. In Nature Genetics 2021. [278] J C Fay and P J Wittkopp. Evaluating the role of natural selection in the evolution of gene regulation. In Heredity 2008.
[279] Aquillah M. Kanzi, James Emmanuel San, Benjamin Chimukangara, and others. Next Generation Sequencing and Bioinformatics Analysis of Family Genetic Inheritance. In Frontiers in Genetics 2020. [280] Gregory A. Wray, Matthew W. Hahn, Ehab Abouheif, and others. The Evolution of Transcriptional Regulation in Eukaryotes. In Molecular Biology and Evolution 2003. [281] Aiping Wu, Lulan Wang, Hang-Yu Zhou, and others. One year of SARS-CoV-2 evolution. In Cell Host & Microbe 2021. [282] Sarah A. Signor and Sergey V. Nuzhdin. The Evolution of Gene Expression in cis and trans. In Trends in Genetics 2018. [283] Andrew Whitehead and Douglas L. Crawford. Variation within and among species in gene expression: raw material for evolution. In Molecular Ecology 2006. [284] Joseph D. Coolon, C. Joel McManus, Kraig R. Stevenson, and others. Tempo and mode of regulatory evolution in Drosophila. In Genome Research 2014. [285] Hans Ellegren. Genome Sequencing and Population Genomics in Non-Model Organisms. In Trends in Ecology & Evolution 2014. [286] Javier Prado-Martinez, Peter H. Sudmant, Jeffrey M. Kidd, and others. Great Ape Genetic Diversity and Population History. In Nature 2013. [287] Ana Prohaska, Fernando Racimo, Andrew J Schork, and others. Human Disease Variation in the Light of Population Genomics. In Cell 2019. [288] Dionisije Sopic, Amin Aminifar, Amir Aminifar, and David Atienza. Real-time event-driven classification technique for early detection and prevention of myocardial infarction on wearable systems. In IEEE TBioCAS 2018. [289] Kyeonghye Guk, Gaon Han, Jaewoo Lim, and others. Evolution of wearable devices with real-time disease monitoring for personalized healthcare. In Nanomaterials 2019. [290] Jonathan Tyler, Sung Won Choi, and Muneesh Tewari. Real-time, personalized medicine through wearable sensors and dynamic predictive modeling: a new paradigm for clinical medicine. In Current Opinion in Systems Biology 2020. [291] Haowen Zhang, Haoran Li, Chirag Jain, and others. Real-time Mapping of Nanopore Raw Signals. In Bioinformatics 2021. [292] Can Firtina, Nika Mansouri Ghiasi, Joel Lindegger, and others. RawHash: enabling fast and accurate real-time analysis of raw nanopore signals for large genomes. In Bioinformatics 2023. [293] Sam Kovaka, Yunfan Fan, Bohan Ni, and others. Targeted Nanopore Sequencing by Real-time Mapping of Raw Electrical Signal with UNCALLED. In Nature Biotechnology 2020. [294] Alexander Payne, Nadine Holmes, Thomas Clarke, and others. Readfish enables targeted nanopore sequencing of gigabase-sized genomes. In Nature Biotechnology 2021. [295] Yuwei Bao, Jack Wadden, John R. Erb-Downward, and others. SquiggleNet: real-time, direct classification of nanopore signals. In Genome Biology 2021. [296] Jens-Uwe Ulrich, Ahmad Lutfi, Kilian Rutzen, and Bernhard Y Renard. ReadBouncer: precise and scalable adaptive sampling for nanopore sequencing. In Bioinformatics 2022. [297] Priyanka Kakria, NK Tripathi, and Peerapong Kitipawang. A real-time health monitoring system for remote cardiac patients using smartphone and wearable sensors. In International Journal of Telemedicine and Applications 2015. [298] Lingxi Wu, Rasool Sharifi, Marzieh Lenjani, and others. Sieve: Scalable in-situ dram-based accelerator designs for massively parallel k-mer matching. In ISCA 2021. [299] Taha Shahroodi, Mahdi Zahedi, Abhairaj Singh, and others. KrakenOnMem: a memristor-augmented HW/SW framework for taxonomic profiling. In ICS 2022. [300] Taha Shahroodi, Mahdi Zahedi, Can Firtina, and others. Demeter: A fast and energy-efficient food profiler using hyperdimensional computing in memory. In IEEE Access 2022. [301] Zuher Jahshan, Itay Merlin, Esteban Garzón, and Leonid Yavits. DASH-CAM: Dynamic Approximate SearcH Content Addressable Memory for genome classification. In MICRO 2023. [302] Robert Hanhan, Esteban Garzón, Zuher Jahshan, and others. EDAM: edit distance tolerant approximate matching content addressable memory. In ISCA 2022. [303] Zhuowen Zou, Hanning Chen, Prathyush Poduval, and others. BioHD: an efficient genome sequence search platform using HyperDimensional memorization. In ISCA 2022. [304] Damla Senol Cali et al. SeGraM: A universal hardware accelerator for genomic sequence-to-graph and sequence-to-sequence mapping. In ISCA 2022. [305] Nika Mansouri Ghiasi, Jisung Park, Harun Mustafa, and others. GenStore: A High-Performance in-Storage Processing System for Genome Sequence Analysis. In ASPLOS 2022. [306] Lingxi Wu, Minxuan Zhou, Weihong Xu, and others. Abakus: Accelerating k-mer Counting With Storage Technology. In TACO 2023. [307] Nika Mansouri Ghiasi, Mohammad Sadrosadati, Harun Mustafa, and others. MegIS: High-Performance, Energy-Efficient, and Low-Cost Metagenomic Analysis with In-Storage Processing. In ISCA 2024.
[308] Sang-Woo Jun, Huy T. Nguyen, Vijay Gadepally, and Arvind. In-storage Embedded Accelerator for Sparse Pattern Processing. In HPEC 2016. [309] Heewoo Kim, Sanjay Sri Vallabh Singapuram, Haojie Ye, and others. NMP-PaK: Near-Memory Processing Acceleration of Scalable De Novo Genome Assembly. In ISCA 2025. [310] You-Kai Zheng, Ming-Liang Wei, Hsiang-Yun Cheng, and others. In-Storage Read-Centric Seed Location Filtering Using 3D-NAND Flash for Genome Sequence Analysis. In ASPDAC 2025. [311] Nika Mansouri Ghiasi, Harun Mustafa, Talu Güloglu, and others. GRAINS: Enabling High-Performance and Low-Cost Graph-Based Genome Analysis via Storage-Aware Algorithm-Architecture Co-Design. In ISCA 2026. [312] Nika Mansouri Ghiasi, Harun Mustafa, Talu Güloglu, and others. GRAINS: Storage-Aware Algorithm-Architecture Co-Design Enabling High-Performance and Low-Cost Graph-Based Genome Analysis. In arXiv 2026. [313] Onur Mutlu, Ataberk Olgun, and İsmail Emir Yüksel. Memory-Centric Computing: Solving Computing’s Memory Problem. In IMW 2025. [314] Onur Mutlu, Saugata Ghose, Juan Gómez-Luna, and Rachata Ausavarungnirun. A Modern Primer on Processing in Memory. In Emerging Computing: From Devices to Systems: Looking Beyond Moore and Von Neumann. 2022. [315] Onur Mutlu, Saugata Ghose, Juan Gómez-Luna, and Rachata Ausavarungnirun. Processing Data Where It Makes Sense: Enabling In-memory Computation. In Microprocessors and Microsystems 2019. [316] Onur Mutlu, Saugata Ghose, Juan Gómez-Luna, and Rachata Ausavarungnirun. Enabling Practical Processing in and Near Memory for Data-Intensive Computing. In DAC 2019. [317] Damla Senol Cali, Jeremie S Kim, Saugata Ghose, and others. Nanopore Sequencing Technology and Tools for Genome Assembly: Computational Analysis of the Current State, Bottlenecks and Future Directions. In Briefings in Bioinformatics 2019. [318] Katherine Yelick, Aydın Buluç, Muaaz Awan, and others. The Parallelism Motifs of Genomic Data Analysis. In Philosophical Transactions of the Royal Society A: Mathematical, Physical and Engineering Sciences 2020. [319] Ruben Langarita, Adria Armejach, Javier Setoain, and others. Compressed Sparse FM-Index: Fast Sequence Alignment Using Large K-Steps . In IEEE/ACM TCBB 2022. [320] Tony Robinson, Jim Harkin, and Priyank Shukla. Hardware Acceleration of Genomics Data Analysis: Challenges and Opportunities. In Bioinformatics 2021. [321] Saugata Ghose, Amirali Boroumand, Jeremie S Kim, and others. Processing-inmemory: A Workload-driven Perspective. In IBM JRD 2019. [322] Michelle M. Li, Kexin Huang, and Marinka Zitnik. Graph Representation Learning in Biomedicine and Healthcare. In Nature Biomedical Engineering 2022. [323] Hai-Cheng Yi, Zhu-Hong You, De-Shuang Huang, and Chee Keong Kwoh. Graph Representation Learning in Bioinformatics: Trends, Methods and Applications. In Briefings in Bioinformatics 2022. [324] Han Yuan. Overcoming Computational Resource Limitations in Deep Learning for Healthcare: Strategies Targeting Data, Model, and Computing. In Medicine Advances 2025. [325] Kamil Khan, Sudeep Pasricha, and Ryan Gary Kim. A Survey of Resource Management for Processing-In-Memory and Near-Memory Processing Architectures. In Journal of Low Power Electronics and Applications 2020. [326] Amir Gholami, Zhewei Yao, Sehoon Kim, and others. AI and Memory Wall. In IEEE Micro 2024. [327] Nicola Rieke, Jonny Hancox, Wenqi Li, and others. The Future of Digital Health with Federated Learning. In npj Digital Medicine 2020. [328] Jie Xu, Benjamin S. Glicksberg, Chang Su, and others. Federated Learning for Healthcare Informatics. In Journal of Healthcare Informatics Research 2021. [329] Georgios A. Kaissis, Marcus R. Makowski, Daniel Rückert, and Rickmer F. Braren. Secure, Privacy-Preserving and Federated Machine Learning in Medical Imaging. In Nature Machine Intelligence 2020. [330] Micah J. Sheller, Brandon Edwards, G. Anthony Reina, and others. Federated Learning in Medicine: Facilitating Multi-Institutional Collaborations Without Sharing Patient Data. In Scientific Reports 2020. [331] Bonan Zhang, Chao Chen, Ickjai Lee, and others. A Survey on Security and Privacy Issues in Wearable Health Monitoring Devices. In Computers & Security 2025. [332] K.A. Sathish Kumar, Leema Nelson, and Betshrine Rachel Jibinsingh. Systematic Review of Privacy-Preserving Federated Learning in Decentralized Healthcare Systems. In Franklin Open 2025. [333] Mikko Rautiainen and Tobias Marschall. GraphAligner: Rapid and Versatile Sequence-to-Graph Alignment. In Genome Biology 2020. [334] Daehwan Kim, Joseph M Paggi, Chanhee Park, and others. Graph-based Genome Alignment and Genotyping with HISAT2 and HISAT-genotype. In Nature Biotechnology 2019. [335] Yan Gao, Yongzhuang Liu, Yanmei Ma, and others. abPOA: an SIMD-based C library for fast partial order alignment using adaptive band. In Bioinformatics 2020.
[336] Chirag Jain, Sanchit Misra, Haowen Zhang, and others. Accelerating Sequence Alignment to Graphs. In IPDPS 2019. [337] Jouni Sirén et al. Pangenomics Enables Genotyping of Known Structural Variants in 5202 Diverse Genomes. In Science 2021. [338] Mikko Rautiainen, Veli Mäkinen, and Tobias Marschall. Bit-parallel sequenceto-graph alignment. In Bioinformatics 2019. [339] Ghanshyam Chandra and Chirag Jain. Sequence to Graph Alignment Using Gap-Sensitive Co-linear Chaining. In RECOMB 2023. [340] Pesho Ivanov, Benjamin Bichsel, and Martin Vechev. Fast and Optimal Sequenceto-Graph Alignment Guided by Seeds. In RECOMB 2022. [341] Jun Ma, Manuel Cáceres, Leena Salmela, and others. Chaining for accurate alignment of erroneous long reads to acyclic variation graphs. In Bioinformatics 2023. [342] Charlotte A Darby, Ravi Gaddipati, Michael C Schatz, and Ben Langmead. Vargas: heuristic-free alignment for assessing linear and graph read aligners. In Bioinformatics 2020. [343] Stephen Hwang, Nathaniel K. Brown, Omar Y. Ahmed, and others. Mem-based pangenome indexing for k-mer queries. In Algorithms for Molecular Biology 2025. [344] Sandra Romain and Claire Lemaitre. SVJedi-graph: improving the genotyping of close and overlapping structural variants with long reads using a variation graph. In Bioinformatics 2023. [345] Heng Li, Xiaowen Feng, and Chong Chu. The design and construction of reference pangenome graphs with minigraph. In Genome Biology 2020. [346] William Andrew Simon, Leonid Yavits, Konstantina Koliogeorgi, and others. Processing-in-Memory for Genomics Workloads. In IEEE Micro 2026. [347] Stephen F Altschul, Warren Gish, Webb Miller, and others. Basic Local Alignment Search Tool. In Journal of Molecular Biology 1990. [348] Lukas Breitwieser et al. BioDynaMo: a modular platform for high-performance agent-based simulation. In Bioinformatics 2022. [349] Lukas Johannes Breitwieser. Design and Analysis of an Extreme-Scale, HighPerformance, and Modular Agent-Based Simulation Platform. In arXiv preprint arXiv:2503.10796 2025. [350] Lukas Breitwieser, Ahmad Hesam, Fons Rademakers, and others. Highperformance and scalable agent-based simulation with biodynamo. In PPoPP 2023. [351] Lukas Breitwieser, Ahmad Hesam, Abdullah Giray Yağlıkçı, and others. TeraAgent: A Distributed Agent-Based Simulation Engine for Simulating Half a Trillion Agents. In arXiv preprint arXiv:2509.24063 2025. [352] Yichi Zhang, Dibei Chen, Gang Zeng, and others. Harp: Leveraging QuasiSequential Characteristics to Accelerate Sequence-to-Graph Mapping of Long Reads. In ASPLOS 2024. [353] Gang Zeng, Jianfeng Zhu, Yichi Zhang, and others. A High-Performance Genomic Accelerator for Accurate Sequence-to-Graph Alignment Using Dynamic Programming Algorithm. In IEEE TPDS 2024. [354] Zhe-Wei Shen, Jheng-Syun Huang, and Yi-Chang Lu. A Memory-Efficient Accelerator for 128-Parallel Sequence-to-Graph Alignment in Variant-Enriched Regions. In BioCAS 2024. [355] Wen-Jun Li, Bhagwan Narayan Rekadwad, Jian-Yu Jiao, and Nimaichand Salam. Exploring Microbial Dark Matter and the Status of Bacterial and Archaeal Taxonomy: Challenges and Opportunities in the Future. In Modern Taxonomy of Bacteria and Archaea: New Methods, Technology and Advances. 2024. [356] Kalikinkar Mandal, Bo Yang, Guang Gong, and Mark Aagaard. Analysis and Efficient Implementations of a Class of Composited de Bruijn Sequences. In IEEE TC 2020. [357] B. Sharat Chandra Varma, Kolin Paul, M. Balakrishnan, and Dominique Lavenier. FAssem: FPGA Based Acceleration of De Novo Genome Assembly. In FCCM 2013. [358] Muaaz Gul Awan, Steven Hofmeyr, Rob Egan, and others. Accelerating large scale de novo metagenome assembly using GPUs. In SC 2021. [359] Zonghao Feng and Qiong Luo. Accelerating Sequence-to-Graph Alignment on Heterogeneous Processors. In ICPP 2021. [360] Yichi Zhang, Jianfeng Zhu, Liangwei Li, and others. A 28-nm 239-bp/𝜇 J Agile Pangenome Analysis Accelerator for Multi-Scheme Read Mapping. In IEEE JSSC 2025. [361] Yu Huang, Long Zheng, Haifeng Liu, and others. MeG2: In-Memory Acceleration for Genome Graphs Analysis. In DAC 2023. [362] Shaahin Angizi, Naima Ahmed Fahmi, Deniz Najafi, and others. PANDA: Processing in Magnetic Random-Access Memory-Accelerated de Bruijn GraphBased DNA Assembly. In Journal of Low Power Electronics and Applications 2024. [363] Shuang Qiu and Qiong Luo. Parallelizing Big De Bruijn Graph Construction on Heterogeneous Processors. In ICDCS 2017. [364] Minxuan Zhou, Lingxi Wu, Muzhou Li, and others. Ultra Efficient Acceleration for De Novo Genome Assembly via Near-Memory Computing. In PACT 2021. [365] Aritra Sarkar, Zaid Al-Ars, and Koen Bertels. QuASeR: Quantum Accelerated de novo DNA sequence reconstruction. In PLOS ONE 2021.
[366] B. Sharat Chandra Varma, Kolin Paul, M. Balakrishnan, and Dominique Lavenier. Hardware acceleration of de novo genome assembly. In International Journal of Embedded Systems 2017. [367] B. Sharat Chandra Varma, Kolin Paul, and M. Balakrishnan. FPGA-Based Acceleration of De Novo Genome Assembly. In Architecture Exploration of FPGA Based Accelerators for BioInformatics Applications. 2016. [368] Sayan Goswami, Kisung Lee, Shayan Shams, and Seung-Jong Park. GPUAccelerated Large-Scale Genome Assembly. In IPDPS 2018. [369] Georgios Galanos, Pavlos Malakonakis, and Apostolos Dollas. An FPGA-Based Data Pre-Processing Architecture to Accelerate De-Novo Genome Assembly. In BIBE 2021. [370] Shaahin Angizi, Naima Ahmed Fahmi, Wei Zhang, and Deliang Fan. PIMAssembler: A Processing-in-Memory Platform for Genome Assembly. In DAC 2020. [371] Aman Sinha, Huei-Chun Yang, Pei-Yi Liu, and others. DSIM: Distributed Sequence Matching on Near-DRAM Accelerator for Genome Assembly. In IEEE Journal on Emerging and Selected Topics in Circuits and Systems 2022. [372] Pingfan Meng, Matthew Jacobsen, Motoki Kimura, and others. Hardware accelerated novel optical de novo assembly for large-scale genomes. In FPL 2014. [373] Yuanqi Hu and Pantelis Georgiou. A Real-Time de novo DNA Sequencing Assembly Platform Based on an FPGA Implementation. In IEEE/ACM TCBB 2016. [374] Yibo Chen, Jun-Han Huang, Yuhui Sun, and others. VRP Assembler: haplotyperesolvedde novoassembly of diploid and polyploid genomes using quantum computing. In Cell Reports Methods 2023. [375] Santhi Natarajan, N. KrishnaKumar, H. V. Anuchan, and others. ReneGENENovo: Co-designed Algorithm-Architecture for Accelerated Preprocessing and Assembly of Genomic Short Reads. In ARC 2018. [376] Shanshan Ren, Nauman Ahmed, Koen Bertels, and Zaid Al-Ars. An Efficient GPU-Based de Bruijn Graph Construction Algorithm for Micro-Assembly. In BIBE 2018. [377] Konstantina Koliogeorgi, Sotirios Xydis, Georgi Gaydadjiev, and Dimitrios Soudris. Gandafl: Dataflow Acceleration for Short Read Alignment on NGS Data. In IEEE TC 2022. [378] Konstantina Koliogeorgi, Dimitrios Soudris, and Sotirios Xydis. Profile-Driven Banded Smith-Waterman acceleration for Short Read Alignment. In DAC 2023. [379] Konstantina Koliogeorgi, Nils Voss, Sotiria Fytraki, and others. Dataflow acceleration of smith-waterman with traceback for high throughput next generation sequencing. In FPL 2019. [380] Vasileios Tsoutsouras, Konstantina Koliogeorgi, Sotirios Xydis, and Dimitrios Soudris. An exploration framework for efficient high-level synthesis of support vector machines: Case study on ecg arrhythmia detection for xilinx zynq soc. In Journal of Signal Processing Systems 2017. [381] Damla Senol. 2021. Accelerating Genome Sequence Analysis via Efficient Hardware/Algorithm Co-Design. Ph. D. Dissertation. Carnegie Mellon University. [382] Gagandeep Singh, Mohammed Alser, Damla Senol Cali, and others. FPGA-based Near-Memory Acceleration of Modern Data-Intensive Applications. In IEEE Micro 2021. [383] Taha Shahroodi, Gagandeep Singh, Mahdi Zahedi, and others. Swordfish: A Framework for Evaluating Deep Neural Network-Based Basecalling Using Computation-In-Memory with Non-Ideal Memristors. In MICRO 2023. [384] Alejandro Alonso-Marín, Ivan Fernandez, Quim Aguado-Puig, and others. BIMSA: Accelerating Long Sequence Alignment Using Processing-In-Memory. In Bioinformatics 2024. [385] Safaa Diab, Amir Nassereldine, Mohammed Alser, and others. High-throughput Pairwise Alignment with the Wavefront Algorithm using Processing-inMemory. In IPDPSW 2022. [386] Nika Mansouri Ghiasi. 2026. Storage-Centric System Designs for Enabling Fast, Efficient, and Low-Cost Genomic and Metagenomic Analyses. Ph. D. Dissertation. ETH Zurich. [387] Nika Mansouri Ghiasi, Jisung Park, Harun Mustafa, and others. GenStore: A High-Performance and Energy-Efficient In-Storage Computing System for Genome Sequence Analysis. In arXiv 2022. [388] Nika Mansouri Ghiasi, Mohammad Sadrosadati, Harun Mustafa, and others. MegIS: High-Performance, Energy-Efficient, and Low-Cost Metagenomic Analysis with In-Storage Processing. In arXiv 2024. [389] Nika Mansouri Ghiasi, Harun Mustafa, Talu Güloglu, and others. GRAINS: Storage-Aware Algorithm-Architecture Co-Design Enabling High-Performance and Low-Cost Graph-Based Genome Analysis. In arXiv 2026. [390] Nika Mansouri Ghiasi, Talu Güloglu, Harun Mustafa, and others. SAGe: A Lightweight Algorithm-Architecture Co-Design for Mitigating the Data Preparation Bottleneck in Large-Scale Genome Sequence Analysis. In HPCA 2026. [391] Nika Mansouri Ghiasi, Talu Güloglu, Harun Mustafa, and others. SAGe: A Lightweight Algorithm-Architecture Co-Design for Mitigating the Data Preparation Bottleneck in Large-Scale Genome Sequence Analysis. In arXiv 2026. [392] Onur Mutlu Lectures. YouTube Channel. [n. d.]. https://www.youtube.com/ @OnurMutluLectures.
[393] The First Workshop on Architecture for Health (Arch4Health). YouTube Livestream. 2025. https://www.youtube.com/watch?v=lTc_gQzFNJI. [394] The Second Workshop on Architecture for Health (Arch4Health). YouTube Livestream. 2026. https://www.youtube.com/watch?v=hSRSZCjnKVo&t. [395] The First Workshop on Architecture for Health (Arch4Health). In conjunction with the 58th IEEE/ACM International Symposium on Microarchitecture (MICRO). 2025. https://events.safari.ethz.ch/micro25-arch4health/. [396] The Second Workshop on Architecture for Health (Arch4Health). In conjunction with the IEEE International Symposium on High-Performance Computer Architecture (HPCA). 2026. https://events.safari.ethz.ch/hpca26-arch4health/. [397] The Third Workshop on Architecture for Health (Arch4Health). In conjunction with the ACM International Conference on Supercomputing 2026 (ICS). 2026. https://events.safari.ethz.ch/ics26-arch4health/. [398] The First Workshop on Systems for Health (Sys4Health). In conjunction with the 32nd Symposium on Operating Systems Principles (SOSP). 2026. https: //events.safari.ethz.ch/sosp26-sys4health/. [399] Mohammed Alser, Zülal Bingöl, Damla Senol Cali, and others. Accelerating Genome Analysis: A Primer on an Ongoing Journey. In IEEE Micro 2020. [400] Damla Senol Cali, Jeremie S Kim, Saugata Ghose, and others. Nanopore Sequencing Technology and Tools for Genome Assembly: Computational Analysis of the Current State, Bottlenecks and Future Directions. In Briefings in Bioinformatics 2018. [401] Can Firtina, Melina Soysal, Joël Lindegger, and Onur Mutlu. RawHash2: Mapping Raw Nanopore Signals Using Hash-Based Seeding and Adaptive Quantization. In Bioinformatics 2024. [402] Can Firtina, Maximilian Mordig, Harun Mustafa, and others. Rawsamble: Overlapping Raw Nanopore Signals using a Hash-based Seeding Mechanism. In Bioinformatics 2026. [403] Joël Lindegger, Can Firtina, Nika Mansouri Ghiasi, and others. RawAlign: Accurate, Fast, and Scalable Raw Nanopore Signal Mapping via Combining Seeding and Alignment. In IEEE Access 2024. [404] Furkan Eris, Ulysse McConnell, Can Firtina, and Onur Mutlu. RawBench: A Comprehensive Benchmarking Framework for Raw Nanopore Signal Analysis Techniques. In BCB 2025. [405] Safaa Diab, Amir Nassereldine, Mohammed Alser, and others. A framework for high-throughput sequence alignment using real processing-in-memory systems. In Bioinformatics 2023. [406] Meryem Banu Cavlak, Gagandeep Singh, Mohammed Alser, and others. TargetCall: Eliminating the Wasted Computation in Basecalling via Pre-BGsecalling Filtering. In Frontiers in Genetics 2024. [407] Jeremie S. Kim, Can Firtina, Meryem Banu Cavlak, and others. AirLift: A Fast and Comprehensive Technique for Remapping Alignments between Reference Genomes. In IEEE/ACM TCBB 2024. [408] Gagandeep Singh, Mohammed Alser, Kristof Denolf, and others. RUBICON: a framework for designing efficient deep learning-based genomic basecallers. In Genome Biology 2024. [409] Can Firtina, Jisung Park, Mohammed Alser, and others. BLEND: a fast, memoryefficient and accurate mechanism to find fuzzy seed matches in genome analysis. In NAR Genomics and Bioinformatics 2023. [410] Can Firtina, Jeremie S Kim, Mohammed Alser, and others. Apollo: A Sequencingtechnology-independent, Scalable and Accurate Assembly Polishing Algorithm. In Bioinformatics 2020. [411] Julian Pavon, Ivan Vargas Valdivieso, Carlos Rojas, and others. QUETZAL: Vector Acceleration Framework for Modern Genome Sequence Analysis Algorithms. In ISCA 2024. [412] Mohammed Alser, Taha Shahroodi, Juan Gómez-Luna, and others. SneakySnake: A Fast and Accurate Universal Genome Pre-alignment Filter for CPUs, GPUs and FPGAs. In Bioinformatics 2020. [413] Mohammed Alser, Hasan Hassan, Hongyi Xin, and others. GateKeeper: A New Hardware Architecture for Accelerating Pre-alignment in DNA Short Read Mapping. In Bioinformatics 2017. [414] Zülal Bingöl, Mohammed Alser, Onur Mutlu, and others. GateKeeper-GPU: Fast and Accurate Pre-Alignment Filtering in Short Read Mapping. In IPDPSW 2021. [415] Mohammed Alser, Hasan Hassan, Akash Kumar, and others. Shouji: A Fast and Efficient Pre-alignment Filter for Sequence Alignment. In Bioinformatics 2019. [416] Jeremie S. Kim, Damla Senol Cali, Hongyi Xin, and others. GRIM-Filter: Fast seed location filtering in DNA read mapping using processing-in-memory technologies. In BMC Genomics 2018. [417] Can Firtina, Kamlesh Pillai, Gurpreet S. Kalsi, and others. ApHMM: Accelerating Profile Hidden Markov Models for Fast and Energy-efficient Genome Analysis. In TACO 2024. [418] Jeremie S Kim, Can Firtina, Meryem Banu Cavlak, and others. FastRemap: a tool for quickly remapping reads between genome assemblies. In Bioinformatics 2022. [419] Joël Lindegger, Damla Senol Cali, Mohammed Alser, and others. Algorithmic Improvement and GPU Acceleration of the GenASM Algorithm. In IPDPSW 2022.
[420] Can Firtina. Enabling Fast, Accurate, and Efficient Real-Time Genome Analysis via New Algorithms and Techniques. In arXiv preprint arXiv:2503.02997 2025. [421] Konstantina Koliogeorgi. Hardware acceleration techniques for computation and data intensive machine learning and bioinformatic applications. In 2023.