Published October 11, 2022 | Version v1
Dataset Open

Data For: Identifying rare variants inconsistent with identity-by-descent in population-scale whole-genome sequencing data

Creators

  • 1. University of Pennsylvania

Description

Simulation output and Genome-wide scan for nIBD variants in UK10K data as reported in:

Identifying rare variants inconsistent with identity-by-descent in population-scale whole-genome sequencing data

Johnson KE, Adams CJ, Voight BF. Methods Ecol Evol 2022 Nov;13(11): 2429–2442.

Code available at: https://github.com/kelsj/EVICORD

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Additional details

Related works

Is published in
Journal article: 10.1111/2041-210X.13991 (DOI)

Funding

Functional Interrogation of T2D-associated genes in human stem cell-derived models and mice 1UM1DK126194-01
National Institutes of Health
Algorithms to identify non-coding mutational burden and disease-relevant pathways 1R01DK101478-01
National Institutes of Health
10,000 UK genome sequences: accessing the role of rare genetic variants in health and disease. 091310
Wellcome Trust
PREDOCTORAL TRAINING PROGRAM IN GENETICS 1T32GM008216-01
National Institutes of Health