PCGC_CHD | NHLBI Trans-Omics for Precision Medicine

PCGC's Congenital Heart Disease Biobank

PCGC_CHD

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)

Progress Report

Status report for Characterizing the Structural Variations in Cardiomyopathy Associated Genes in the NHLBI TOPMed Program (Prop ID:14705)

Abstracts associated with this proposal

Unveiling the Hidden Rules: Enhancing NMD Prediction for Protein-Truncating Variants

Progress Report

Status report for Systematic profiling and characterization of transcripts that are associated with quantitative blood disease traits through putative gain-of-function variants (Prop ID:14437)

Progress Report

Status report for Somatic variant associations in non-CHIP carriers with frailty, biological aging and atherosclerosis (Prop ID:13934)

Progress Report

Status report for Estimating ancestry-specific allele frequencies in admixed samples from large-scale sequencing data. (Prop ID:12704)

Progress Report

Status report for Association study of the genetic determinants of hematopoietic stem cell single-base substitution signature (Prop ID:12731)