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

Erica K. Barnell(Washington University in St. Louis), Obi L. Griffith(Washington University in St. Louis), Benjamin J. Ainscough(James S. McDonnell Foundation), Alina Schmidt(Washington University in St. Louis), Arpad Danos(James S. McDonnell Foundation), Kelsy C. Cotto(James S. McDonnell Foundation), Malachi Griffith(Washington University in St. Louis), Jason Kunisaki(James S. McDonnell Foundation), Lana Sheta(James S. McDonnell Foundation), Alex H. Wagner(James S. McDonnell Foundation), Peter Ronning(James S. McDonnell Foundation), Zachary L. Skidmore(James S. McDonnell Foundation), Katie M. Campbell(University of California, Los Angeles), Jasreet Hundal(James S. McDonnell Foundation), Felicia Gomez(James S. McDonnell Foundation), Nicholas C. Spies(James S. McDonnell Foundation), Lee Trani(James S. McDonnell Foundation), Kilannin Krysiak(James S. McDonnell Foundation), Malik S. Sediqzad(James S. McDonnell Foundation), Cody A. Ramirez(James S. McDonnell Foundation), Matthew K. Matlock(James S. McDonnell Foundation), S. Joshua Swamidass(Washington University in St. Louis), Megan M. Richters(James S. McDonnell Foundation), Shahil Pema(James S. McDonnell Foundation)
Genetics in Medicine
October 3, 2018
Cited by 118


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