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Paper Details

Standard operating procedure for somatic variant refinement of sequencing data with paired tumor and normal samples.
Genet Med
50
2019
SOP, aligned read, aligned read sequences, normal samples, somatic variant, somatic variants, tags, tumor
Algorithms, High-Throughput Nucleotide Sequencing, Humans, Mutation, Neoplasms, Polymorphism, Single Nucleotide, Sequence Alignment, Software
Author NameAffiliation
Erica K BarnellMcDonnell Genome Institute, Washington University School of Medicine
Peter RonningMcDonnell Genome Institute, Washington University School of Medicine
Katie M CampbellMcDonnell Genome Institute, Washington University School of Medicine
Kilannin KrysiakMcDonnell Genome Institute, Washington University School of Medicine
Kilannin KrysiakWashington University School of Medicine
Benjamin J AinscoughMcDonnell Genome Institute, Washington University School of Medicine
Benjamin J AinscoughSiteman Cancer Center, Washington University School of Medicine
Lana M ShetaMcDonnell Genome Institute, Washington University School of Medicine
Shahil P PemaMcDonnell Genome Institute, Washington University School of Medicine
Alina D SchmidtMcDonnell Genome Institute, Washington University School of Medicine
Megan M RichtersMcDonnell Genome Institute, Washington University School of Medicine
Kelsy C CottoMcDonnell Genome Institute, Washington University School of Medicine
Arpad M DanosMcDonnell Genome Institute, Washington University School of Medicine
Cody A RamirezMcDonnell Genome Institute, Washington University School of Medicine
Zachary L SkidmoreMcDonnell Genome Institute, Washington University School of Medicine
Nicholas C SpiesMcDonnell Genome Institute, Washington University School of Medicine
Jasreet HundalMcDonnell Genome Institute, Washington University School of Medicine
Malik S SediqzadMcDonnell Genome Institute, Washington University School of Medicine
Jason KunisakiMcDonnell Genome Institute, Washington University School of Medicine
Felicia GomezMcDonnell Genome Institute, Washington University School of Medicine
Lee TraniMcDonnell Genome Institute, Washington University School of Medicine
Matthew K MatlockMcDonnell Genome Institute, Washington University School of Medicine
Alex H WagnerMcDonnell Genome Institute, Washington University School of Medicine
Sanjay J SwamidassWashington University School of Medicine
Sanjay J SwamidassInstitute for Informatics, Washington University School of Medicine
Malachi GriffithMcDonnell Genome Institute, Washington University School of Medicine
Malachi GriffithWashington University School of Medicine
Malachi GriffithSiteman Cancer Center, Washington University School of Medicine
Malachi GriffithWashington University School of Medicine
Obi L GriffithMcDonnell Genome Institute, Washington University School of Medicine
Obi L GriffithWashington University School of Medicine
Obi L GriffithSiteman Cancer Center, Washington University School of Medicine
Obi L GriffithWashington University School of Medicine
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