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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Bibliografiske detaljer
Udgivet i:PLoS One
Main Authors: Decap, Dries, Reumers, Joke, Herzeel, Charlotte, Costanza, Pascal, Fostier, Jan
Format: Artigo
Sprog:Inglês
Udgivet: Public Library of Science 2017
Fag:
Research Article
Online adgang: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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