HAL (France)open access
COBT: a gene-based rare variant burden test for case-only study designs using aggregated genotypes from public reference cohorts
Rare diseases, Ciliopathies, Case-only association analysis, 0, Statistical genetics, Burden testing
This document is indexed with metadata only — full text is not available in the archive for this record.
Open the official source ↗
Record · ID 274310
Retrieved via
Conceptio — every document is proof-bundled with source, license, and retrieval metadata.