Crossmark

Standard operating procedure for somatic variant refinement of sequencing data with paired tumor and normal samples

Crossref DOI link: https://doi.org/10.1038/s41436-018-0278-z

Published Print: 2019-04

Update policy: https://doi.org/10.1016/elsevier_cm_policy

Authors

Barnell, Erica K.

Ronning, Peter

Campbell, Katie M.

Krysiak, Kilannin

Ainscough, Benjamin J.

Sheta, Lana M.

Pema, Shahil P.

Schmidt, Alina D.

Richters, Megan

Cotto, Kelsy C.

Danos, Arpad M.

Ramirez, Cody

Skidmore, Zachary L.

Spies, Nicholas C.

Hundal, Jasreet

Sediqzad, Malik S.

Kunisaki, Jason

Gomez, Felicia

Trani, Lee

Matlock, Matthew

Wagner, Alex H.

Swamidass, S. Joshua

Griffith, Malachi

Griffith, Obi L.
License Information

Text and Data Mining valid from 2019-04-01

Text and Data Mining valid from 2019-04-01

Version of Record valid from 2021-11-24
More Information

This article is maintained by: Elsevier

Article Title: Standard operating procedure for somatic variant refinement of sequencing data with paired tumor and normal samples

Journal Title: Genetics in Medicine

CrossRef DOI link to publisher maintained version: https://doi.org/10.1038/s41436-018-0278-z

Content Type: article

Copyright: © 2019, The Author(s), under exclusive licence to the American College of Medical Genetics and Genomics