Abstract:
BACKGROUND:RNA sequencing has become an increasingly affordable way to profile gene expression patterns. Here we introduce a workflow implementing several open-source softwares that can be run on a high performance computing environment. RESULTS:Developed as a tool by the Bioinformatics Shared Resource Group (BISR) at the Ohio State University, we have applied the pipeline to a few publicly available RNAseq datasets downloaded from GEO in order to demonstrate the feasibility of this workflow. Source code is available here: workflow: https://code.bmi.osumc.edu/gadepalli.3/BISR-RNAseq-ICIBM2019 and shiny: https://code.bmi.osumc.edu/gadepalli.3/BISR_RNASeq_ICIBM19. Example dataset is demonstrated here: https://dataportal.bmi.osumc.edu/RNA_Seq/. CONCLUSION:The workflow allows for the analysis (alignment, QC, gene-wise counts generation) of raw RNAseq data and seamless integration of quality analysis and differential expression results into a configurable R shiny web application.
journal_name
BMC Bioinformaticsjournal_title
BMC bioinformaticsauthors
Gadepalli VS,Ozer HG,Yilmaz AS,Pietrzak M,Webb Adoi
10.1186/s12859-019-3251-1subject
Has Abstractpub_date
2019-12-20 00:00:00pages
670issue
Suppl 24issn
1471-2105pii
10.1186/s12859-019-3251-1journal_volume
20pub_type
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