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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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| Publicat a: | Bioinformatics |
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| Autors principals: | , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Oxford University Press
2019
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| Matèries: | |
| Accés en línia: | 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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