Massively parallel enrichment of low-frequency alleles enables duplex sequencing at low depth-Reference-Cited by-同舟云学术

Massively parallel enrichment of low-frequency alleles enables duplex sequencing at low depth

Published:2022-03-17 Issue:3 Volume:6 Page:257-266
ISSN:2157-846X
Container-title:Nature Biomedical Engineering
language:en
Short-container-title:Nat. Biomed. Eng

Author:

Gydush Gregory,Nguyen Erica,Bae Jin H.^ORCID,Blewett Timothy,Rhoades Justin,Reed Sarah C.,Shea Douglas,Xiong Kan,Liu Ruolin^ORCID,Yu Fangyan,Leong Ka Wai,Choudhury Atish D.^ORCID,Stover Daniel G.,Tolaney Sara M.^ORCID,Krop Ian E.,Christopher Love J.^ORCID,Parsons Heather A.^ORCID,Mike Makrigiorgos G.^ORCID,Golub Todd R.^ORCID,Adalsteinsson Viktor A.^ORCID

Funder

U.S. Department of Health & Human Services | National Institutes of Health

Gerstner Family Foundation

Publisher

Springer Science and Business Media LLC

Subject

Computer Science Applications,Biomedical Engineering,Medicine (miscellaneous),Bioengineering,Biotechnology

Link

https://www.nature.com/articles/s41551-022-00855-9.pdf

Reference51 articles.

1. Luquette, L. J., Bohrson, C. L., Sherman, M. A. & Park, P. J. Identification of somatic mutations in single cell DNA-seq using a spatial model of allelic imbalance. Nat. Commun. 10, 3908 (2019).

2. Ludwig, L. S. et al. Lineage tracing in humans enabled by mitochondrial mutations and single-cell genomics. Cell 176, e22 (2019).