RNA-Seq Alignment to Individualized Genomes Improves Transcript Abundance Estimates in Multiparent Populations

Massively parallel RNA sequencing (RNA-seq) has yielded a wealth of new insights into transcriptional regulation. A first step in the analysis of RNA-seq data is the alignment of short sequence reads to a common reference genome or transcriptome. Genetic variants that distinguish individual genomes...

Deskribapen osoa

Gorde:
Xehetasun bibliografikoak
Egile Nagusiak: Munger, Steven C., Raghupathy, Narayanan, Choi, Kwangbom, Simons, Allen K., Gatti, Daniel M., Hinerfeld, Douglas A., Svenson, Karen L., Keller, Mark P., Attie, Alan D., Hibbs, Matthew A., Graber, Joel H., Chesler, Elissa J., Churchill, Gary A.
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: Genetics Society of America 2014
Gaiak:
Multiparental Populations
Sarrera elektronikoa:https://ncbi.nlm.nih.gov/pmc/articles/PMC4174954/
https://ncbi.nlm.nih.gov/pubmed/25236449
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1534/genetics.114.165886
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