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ScanIndel: a hybrid framework for indel detection via gapped alignment, split reads and de novo assembly
Comprehensive identification of insertions/deletions (indels) across the full size spectrum from second generation sequencing is challenging due to the relatively short read length inherent in the technology. Different indel calling methods exist but are limited in detection to specific sizes with v...
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| Publicado no: | Genome Med |
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| Main Authors: | , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BioMed Central
2015
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4671222/ https://ncbi.nlm.nih.gov/pubmed/26643039 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s13073-015-0251-2 |
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