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SNVHMM: predicting single nucleotide variants from next generation sequencing
BACKGROUND: The rapid development of next generation sequencing (NGS) technology provides a novel avenue for genomic exploration and research. Single nucleotide variants (SNVs) inferred from next generation sequencing are expected to reveal gene mutations in cancer. However, NGS has lower sequence c...
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| Hauptverfasser: | , , , , , |
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| Format: | Artigo |
| Sprache: | Inglês |
| Veröffentlicht: |
BioMed Central
2013
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| Schlagworte: | |
| Online Zugang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3718670/ https://ncbi.nlm.nih.gov/pubmed/23855743 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1471-2105-14-225 |
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