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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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Bibliografski detalji
Izdano u:PLoS One
Glavni autori: Decap, Dries, Reumers, Joke, Herzeel, Charlotte, Costanza, Pascal, Fostier, Jan
Format: Artigo
Jezik:Inglês
Izdano: Public Library of Science 2017
Teme:
Online pristup: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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