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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...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6735753/ https://www.ncbi.nlm.nih.gov/pubmed/30649250 http://dx.doi.org/10.1093/bioinformatics/btz033 |