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Using population data for assessing next-generation sequencing performance
Motivation: During the past 4 years, whole-exome sequencing has become a standard tool for finding rare variants causing Mendelian disorders. In that time, there has also been a proliferation of both sequencing platforms and approaches to analyse their output. This requires approaches to assess the...
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| Publicado no: | Bioinformatics |
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| Main Authors: | , , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Oxford University Press
2015
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4271148/ https://ncbi.nlm.nih.gov/pubmed/25236458 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/bioinformatics/btu606 |
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