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SNPAAMapper: An efficient genome-wide SNP variant analysis pipeline for next-generation sequencing data
Many NGS analysis tools focusing on read alignment and variant calling functions for exome sequencing data have been developed in recent years. However, publicly available tools dealing with the downstream analysis of genome-wide variants are fewer and have limited functionality. We developed SNPAAM...
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| Asıl Yazarlar: | , |
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| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
Biomedical Informatics
2013
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| Konular: | |
| Online Erişim: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3819573/ https://ncbi.nlm.nih.gov/pubmed/24250114 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.6026/97320630009870 |
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