bioRxiv · 10.1101/2021.02.06.430068
High coverage whole genome sequencing of the expanded 1000 Genomes Project cohort including 602 trios
Abstract
The 1000 Genomes Project (1kGP) is the largest fully open resource of whole genome sequencing (WGS) data consented for public distribution of raw sequence data without access or use restrictions. The final release of the 1kGP included 2,504 unrelated samples from 26 populations and was based primarily on low coverage WGS. Here, we present a new, high coverage 3,202-sample WGS 1kGP resource, sequenced to a targeted depth of 30X using the Illumina NovaSeq 6000 system, which now includes 602 complete trios. We performed SNV/INDEL calling against the GRCh38 reference using GATKs HaplotypeCaller, and generated a comprehensive set of SVs by integrating multiple analytic methods through a sophisticated machine learning model. We make all the data generated as part of this project publicly available and we envision it to become the new de facto public resource for the worldwide genomics and genetics community.
Source connections
Explore related subjects
Keep this discovery
Explore connections, maps & timelines
Byrska-Bishop, M., Evani, U. S., Zhao, X., Basile, A. O., Abel, H. J., Regier, A. A., Corvelo, A., Clarke, W. E., Musunuri, R., Nagulapalli, K., Fairley, S., Runnels, A., Winterkorn, L., Lowy-Gallego, E., The Human Genome Structural Variation Consortium,, Flicek, P., Germer, S., Brand, H., Hall, I. M., Talkowski, M. E., Narzisi, G., Zody, M. C.. 2021-02-07. High coverage whole genome sequencing of the expanded 1000 Genomes Project cohort including 602 trios. https://doi.org/10.1101/2021.02.06.430068
Cite the original work for its findings. Save a collection to share your selection of sources.