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Improved indel detection in DNA and RNA via realignment with ABRA2

MOTIVATION: Genomic variant detection from next-generation sequencing has become established as an extremely important component of research and clinical diagnoses in both cancer and Mendelian disorders. Insertions and deletions (indels) are a common source of variation and can frequently impact fun...

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Bibliografski detalji
Izdano u:Bioinformatics
Glavni autori: Mose, Lisle E, Perou, Charles M, Parker, Joel S
Format: Artigo
Jezik:Inglês
Izdano: Oxford University Press 2019
Teme:
Online pristup:https://ncbi.nlm.nih.gov/pmc/articles/PMC6735753/
https://ncbi.nlm.nih.gov/pubmed/30649250
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/bioinformatics/btz033
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