Best practices on the differential expression analysis of multi-species RNA-seq

被引:0
作者
Matthew Chung
Vincent M. Bruno
David A. Rasko
Christina A. Cuomo
José F. Muñoz
Jonathan Livny
Amol C. Shetty
Anup Mahurkar
Julie C. Dunning Hotopp
机构
[1] University of Maryland School of Medicine,Institute for Genome Sciences
[2] University of Maryland School of Medicine,Department of Microbiology and Immunology
[3] Infectious Disease and Microbiome Program,Greenebaum Cancer Center
[4] Broad Institute,undefined
[5] University of Maryland,undefined
来源
Genome Biology | / 22卷
关键词
RNA-Seq; Transcriptomics; Best practices; Differential gene expression;
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摘要
Advances in transcriptome sequencing allow for simultaneous interrogation of differentially expressed genes from multiple species originating from a single RNA sample, termed dual or multi-species transcriptomics. Compared to single-species differential expression analysis, the design of multi-species differential expression experiments must account for the relative abundances of each organism of interest within the sample, often requiring enrichment methods and yielding differences in total read counts across samples. The analysis of multi-species transcriptomics datasets requires modifications to the alignment, quantification, and downstream analysis steps compared to the single-species analysis pipelines. We describe best practices for multi-species transcriptomics and differential gene expression.
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