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Evaluating Variant Calling Tools for Non-Matched Next-Generation Sequencing Data
Valid variant calling results are crucial for the use of next-generation sequencing in clinical routine. However, there are numerous variant calling tools that usually differ in algorithms, filtering strategies, recommendations and thus, also in the output. We evaluated eight open-source tools regar...
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| Vydáno v: | Sci Rep |
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| Hlavní autoři: | , , , , , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
Nature Publishing Group
2017
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5324109/ https://ncbi.nlm.nih.gov/pubmed/28233799 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/srep43169 |
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