Use of >100,000 NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium whole genome sequences improves imputation quality and detection of rare variant associations in admixed African and Hispanic/Latino populations
Madeline H. Kowalski(New York Genome Center), Yun Li(Shanghai University of Traditional Chinese Medicine)
Cited by 321
Related Papers
Dictionary learning for integrative, multimodal and scalable single-cell analysis
|Nature Biotechnology|2023|4.9k
Dictionary learning for integrative, multimodal, and scalable single-cell analysis
|bioRxiv (Cold Spring Harbor Laboratory)|2022|282
Imputation of Exome Sequence Variants into Population- Based Samples and Blood-Cell-Trait-Associated Loci in African Americans: NHLBI GO Exome Sequencing Project
|The American Journal of Human Genetics|2012|151
Common variants contribute to intrinsic human brain functional networks
|Nature Genetics|2022|148