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Improved Variant Calling Accuracy by Merging Replicates in Whole-Exome Sequencing Studies
In large scale population-based whole-exome sequencing (WES) studies, there are some samples occasionally sequenced two or more times due to a variety of reasons. To investigate how to efficiently utilize these duplicated sequencing data, we conducted comprehensive evaluation of variant calling stra...
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| Main Authors: | , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Hindawi Publishing Corporation
2014
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4137624/ https://ncbi.nlm.nih.gov/pubmed/25162009 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1155/2014/319534 |
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