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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Detalles Bibliográficos
Autores principales: Decap, Dries, Reumers, Joke, Herzeel, Charlotte, Costanza, Pascal, Fostier, Jan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2017
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5373595/
https://www.ncbi.nlm.nih.gov/pubmed/28358893
http://dx.doi.org/10.1371/journal.pone.0174575

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5373595/
https://www.ncbi.nlm.nih.gov/pubmed/28358893
http://dx.doi.org/10.1371/journal.pone.0174575

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