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Halvade-RNA: Parallel variant calling from transcriptomic data using MapReduce
Given the current cost-effectiveness of next-generation sequencing, the amount of DNA-seq and RNA-seq data generated is ever increasing. One of the primary objectives of NGS experiments is calling genetic variants. While highly accurate, most variant calling pipelines are not optimized to run effici...
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| Publicado no: | PLoS One |
|---|---|
| Main Authors: | , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Public Library of Science
2017
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5373595/ https://ncbi.nlm.nih.gov/pubmed/28358893 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0174575 |
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