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INDELseek: detection of complex insertions and deletions from next-generation sequencing data
BACKGROUND: Complex insertions and deletions (indels) from next-generation sequencing (NGS) data were prone to escape detection by currently available variant callers as shown by large-scale human genomics studies. Somatic and germline complex indels in key disease driver genes could be missed in NG...
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| I publikationen: | BMC Genomics |
|---|---|
| Huvudupphovsmän: | , , , , |
| Materialtyp: | Artigo |
| Språk: | Inglês |
| Publicerad: |
BioMed Central
2017
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| Ämnen: | |
| Länkar: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5217656/ https://ncbi.nlm.nih.gov/pubmed/28056804 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12864-016-3449-9 |
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