At present, low-pass whole-genome sequencing (WGS) is frequently used in clinical research and in the screening of copy number variations (CNVs). However, there are still some challenges in the detect
Recents studies in mammalian genomes have uncovered the extent of copy number variation (CNV) that contributes to phenotypic diversity, including health and disease status. Here we report the first gl
Additional file 5. The list of DDG2P genes used in our analysis. Description: The list of DDG2P genes used in our analysis to detect genes overlapping with Bantu CNV blocks.
