The eSNV-detect: a computational system to identify expressed single nucleotide variants from transcriptome sequencing data

Rapid development of next generation sequencing technology has enabled the identification of genomic alterations from short sequencing reads. There are a number of software pipelines available for calling single nucleotide variants from genomic DNA but, no comprehensive pipelines to identify, annota...

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Detalles Bibliográficos
Autores principales: Tang, Xiaojia, Baheti, Saurabh, Shameer, Khader, Thompson, Kevin J., Wills, Quin, Niu, Nifang, Holcomb, Ilona N., Boutet, Stephane C., Ramakrishnan, Ramesh, Kachergus, Jennifer M., Kocher, Jean-Pierre A., Weinshilboum, Richard M., Wang, Liewei, Thompson, E. Aubrey, Kalari, Krishna R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2014
Materias:
Methods Online
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4267611/
https://www.ncbi.nlm.nih.gov/pubmed/25352556
http://dx.doi.org/10.1093/nar/gku1005

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4267611/
https://www.ncbi.nlm.nih.gov/pubmed/25352556
http://dx.doi.org/10.1093/nar/gku1005

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