4.7 Article

MU2A-reconciling the genome and transcriptome to determine the effects of base substitutions

Journal

BIOINFORMATICS
Volume 27, Issue 3, Pages 416-418

Publisher

OXFORD UNIV PRESS
DOI: 10.1093/bioinformatics/btq658

Keywords

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Funding

  1. National Cancer Institute [1 P50 CA121974]
  2. Melanoma Research Alliance
  3. Yale School of Medicine

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Motivation: Next-generation sequencing technologies enable the identification of sequence variation in the genome and transcriptome. Differences between the reference genome and transcript libraries complicate the determination of the effect of genomic sequence variants on protein products; similarly, these differences complicate the mapping of sequence variants found in transcripts to their respective genomic position. We have developed MU2A, a publicly available web service for variant annotation that reconciles differences between the genome and transcriptome, enabling the rapid and accurate determination of the effects of genomic variants on protein products, and the mapping of variants detected in transcripts to genomic coordinates. The MU2A web service is available at http://krauthammerlab.med.yale.edu/mu2a. We have released MU2A as open source, available at http://code.google.com/p/mu2a/.

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