RNA-sequencing (RNA-seq) has a wide variety of applications, but no single analysis pipeline can be used in all cases. We review all of the major steps in RNA-seq data analysis, including experimental design, quality control, read alignment, quantification of gene and transcript levels, visualization, differential gene expression, alternative splicing, functional analysis, gene fusion detection and eQTL mapping. We highlight the challenges associated with each step. We discuss the analysis of small RNAs and the integration of RNA-seq with other functional genomics techniques. Finally, we discuss the outlook for novel technologies that are changing the state of the art in transcriptomics.
Description
A survey of best practices for RNA-seq data analysis. - PubMed - NCBI
%0 Journal Article
%1 Conesa:2016:Genome-Biol:26813401
%A Conesa, A
%A Madrigal, P
%A Tarazona, S
%A Gomez-Cabrero, D
%A Cervera, A
%A McPherson, A
%A Szcześniak, M W
%A Gaffney, D J
%A Elo, L L
%A Zhang, X
%A Mortazavi, A
%D 2016
%J Genome Biol
%K READ best-practice fulltext rna-seq
%P 13-13
%R 10.1186/s13059-016-0881-8
%T A survey of best practices for RNA-seq data analysis
%U https://www.ncbi.nlm.nih.gov/pubmed/26813401
%V 17
%X RNA-sequencing (RNA-seq) has a wide variety of applications, but no single analysis pipeline can be used in all cases. We review all of the major steps in RNA-seq data analysis, including experimental design, quality control, read alignment, quantification of gene and transcript levels, visualization, differential gene expression, alternative splicing, functional analysis, gene fusion detection and eQTL mapping. We highlight the challenges associated with each step. We discuss the analysis of small RNAs and the integration of RNA-seq with other functional genomics techniques. Finally, we discuss the outlook for novel technologies that are changing the state of the art in transcriptomics.
@article{Conesa:2016:Genome-Biol:26813401,
abstract = {RNA-sequencing (RNA-seq) has a wide variety of applications, but no single analysis pipeline can be used in all cases. We review all of the major steps in RNA-seq data analysis, including experimental design, quality control, read alignment, quantification of gene and transcript levels, visualization, differential gene expression, alternative splicing, functional analysis, gene fusion detection and eQTL mapping. We highlight the challenges associated with each step. We discuss the analysis of small RNAs and the integration of RNA-seq with other functional genomics techniques. Finally, we discuss the outlook for novel technologies that are changing the state of the art in transcriptomics.},
added-at = {2017-05-20T16:14:09.000+0200},
author = {Conesa, A and Madrigal, P and Tarazona, S and Gomez-Cabrero, D and Cervera, A and McPherson, A and Szcześniak, M W and Gaffney, D J and Elo, L L and Zhang, X and Mortazavi, A},
biburl = {https://www.bibsonomy.org/bibtex/2cffee95f544de5bea75be3cb32d1e364/marcsaric},
description = {A survey of best practices for RNA-seq data analysis. - PubMed - NCBI},
doi = {10.1186/s13059-016-0881-8},
interhash = {2860e635dab5e884d17c6a4b824b13db},
intrahash = {cffee95f544de5bea75be3cb32d1e364},
journal = {Genome Biol},
keywords = {READ best-practice fulltext rna-seq},
month = jan,
pages = {13-13},
pmid = {26813401},
timestamp = {2017-10-08T00:15:51.000+0200},
title = {A survey of best practices for RNA-seq data analysis},
url = {https://www.ncbi.nlm.nih.gov/pubmed/26813401},
volume = 17,
year = 2016
}