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FamSeq: A Variant Calling Program for Family-Based Sequencing Data Using Graphics Processing Units
Various algorithms have been developed for variant calling using next-generation sequencing data, and various methods have been applied to reduce the associated false positive and false negative rates. Few variant calling programs, however, utilize the pedigree information when the family-based sequ...
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| Huvudupphovsmän: | , , |
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| Materialtyp: | Artigo |
| Språk: | Inglês |
| Publicerad: |
Public Library of Science
2014
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| Ämnen: | |
| Länkar: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4214554/ https://ncbi.nlm.nih.gov/pubmed/25357123 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pcbi.1003880 |
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