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Seplyarskiy, Vladimir |
Population sequencing data reveal a compendium of mutational processes in the human germ line
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2020 |
10.1101/2020.01.10.893024v1 |
|
Jun, Goo |
Multiethnic catalog of structural variants and their translational impact for disease phenotypes across 19,652 genomes
|
2020 |
10.1101/2020.05.02.074096 |
|
Hecker, Julian |
A unifying framework for rare variant association testing in family-based designs, including higher criticism approaches, SKATs, and burden tests
|
2019 |
|
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Bick, Alexander |
Inherited causes of clonal haematopoiesis in 97,691 whole genomes
|
2019 |
10.1101/782748v1 |
|
Mathias, Rasika |
Genetic determinants of telomere length from 109,122 ancestrally diverse whole-genome sequences in TOPMed
|
2019 |
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|
Willer, Cristen |
Loss-of-function genomic variants highlight potential therapeutic targets for cardiovascular disease
|
2019 |
10.1101/597377v1 |
|
Visscher, Peter |
Assessing the contribution of rare variants to complex trait heritability from whole-genome sequence data
|
2019 |
10.1101/588020v1 |
|
Cade, Brian |
Whole-Genome Association Analyses of Sleep-disordered Breathing Phenotypes in the NHLBI TOPMed Program
|
2019 |
10.1101/652966v1 |
|
Taliun, Daniel |
Sequencing of 53,831 diverse genomes from the NHLBI TOPMed Program
|
2019 |
10.1101/563866v1 |
|
Taliun, Daniel |
Sequencing of 53,831 diverse genomes from the NHLBI TOPMed Program
|
2019 |
10.1101/563866v1 |
