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RNA-seq-based mapping and candidate identification of mutations from forward genetic screens.

ABSTRACT: Forward genetic screens have elucidated molecular pathways required for innumerable aspects of life; however, identifying the causal mutations from such screens has long been the bottleneck in the process, particularly in vertebrates. We have developed an RNA-seq-based approach that identifies both the region of the genome linked to a mutation and candidate lesions that may be causal for the phenotype of interest. We show that our method successfully identifies zebrafish mutations that cause nonsense or missense changes to codons, alter transcript splicing, or alter gene expression levels. Furthermore, we develop an easily accessible bioinformatics pipeline allowing for implementation of all steps of the method. Overall, we show that RNA-seq is a fast, reliable, and cost-effective method to map and identify mutations that will greatly facilitate the power of forward genetics in vertebrate models.

SUBMITTER: Miller AC

PROVIDER: S-EPMC3613584 | biostudies-literature | 2013 Apr

REPOSITORIES: biostudies-literature

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RNA-seq-based mapping and candidate identification of mutations from forward genetic screens.

Miller Adam C AC Obholzer Nikolaus D ND Shah Arish N AN Megason Sean G SG Moens Cecilia B CB

Genome research 20130108 4

Forward genetic screens have elucidated molecular pathways required for innumerable aspects of life; however, identifying the causal mutations from such screens has long been the bottleneck in the process, particularly in vertebrates. We have developed an RNA-seq-based approach that identifies both the region of the genome linked to a mutation and candidate lesions that may be causal for the phenotype of interest. We show that our method successfully identifies zebrafish mutations that cause non ...[more]

PMID: 23299976

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Dataset Information

RNA-seq-based mapping and candidate identification of mutations from forward genetic screens.

Publications

RNA-seq-based mapping and candidate identification of mutations from forward genetic screens.

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