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DeNovoGear: de novo indel and point mutation discovery and phasing
We present the DeNovoGear software for analyzing de novo mutations from familial and somatic tissue sequencing data. DeNovoGear uses likelihood-based error modeling to reduce the false positive rate of mutation discovery in exome analysis, and fragment information to identify the parental origin of...
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| Main Authors: | , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2013
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4003501/ https://ncbi.nlm.nih.gov/pubmed/23975140 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/nmeth.2611 |
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