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Vindel: a simple pipeline for checking indel redundancy
BACKGROUND: With the advance of next generation sequencing (NGS) technologies, a large number of insertion and deletion (indel) variants have been identified in human populations. Despite much research into variant calling, it has been found that a non-negligible proportion of the identified indel v...
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| Publié dans: | BMC Bioinformatics |
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| Auteurs principaux: | , , , |
| Format: | Artigo |
| Langue: | Inglês |
| Publié: |
BioMed Central
2014
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| Sujets: | |
| Accès en ligne: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4245841/ https://ncbi.nlm.nih.gov/pubmed/25407965 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12859-014-0359-1 |
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