THRV | NHLBI Trans-Omics for Precision Medicine

THRV

Abstracts associated with this proposal

AI-STAAR: An ancestry-informed association analysis framework for large-scale multi-ancestry whole genome sequencing studies

Progress Report

Status report for An ancestry-informed association analysis framework of large-scale whole genome sequencing studies, with applications to TOPMed kidney data (Prop ID:17930)

Progress Report

Status report for Whole genome sequencing study of blood pressure responses to interventions (Prop ID:10341)

Progress Report

Status report for Increasing genetic and environmental diversity: Multi-ancestry genome-wide study of tobacco and alcohol use in 6.5 million individuals (Prop ID:17628)

Progress Report

Status report for Genome-wide association analyses in the presence of heterogeneous genetic effect on T2D (Prop ID:17524)

Abstracts associated with this proposal

Rare variants affecting telomere length and disease identified through multi-omic modeling

Progress Report

Status report for Watershed multi-omics modeling to identify rare variants affecting telomere length (Prop ID:17322)

Progress Report

Status report for Assessing genetic determinants of telomere length leveraging whole genome sequence data in the NHLBI Trans-Omics for Precision Medicine Program – breakout proposal for PRS. (Prop ID:16887)

Progress Report

Status report for Patterns of ultra-rare genetic variation from high coverage whole genome sequencing of over 150,000 diverse people. (Prop ID:16344)

Abstracts associated with this proposal

Deciphering rare non-coding LDL-C associations in over 246K individuals with whole genome sequencing

Progress Report

Status report for Deciphering rare non-coding lipid associations using whole genome sequencing meta-analysis (Prop ID:15536)

Progress Report

Status report for (Revised) Replication of rare non-coding anthropometric trait associations from whole genome sequencing (Prop ID:15383)

Progress Report

Status report for Replication of rare non-coding anthropometric trait associations from whole genome sequencing (Prop ID:15333)