Abstract
Differential expression analysis of RNA sequencing (RNA-seq) data typically relies on reconstructing transcripts or counting reads that overlap known gene structures. We previously introduced an intermediate statistical approach called differentially expressed region (DER) finder that seeks to identify contiguous regions of the genome showing differential expression signal at single base resolution without relying on existing annotation or potentially inaccurate transcript assembly. We present the derfinder software that improves our annotation-agnostic approach to RNA-seq analysis by: (i) implementing a computationally efficient bump-hunting approach to identify DERs that permits genome-scale analyses in a large number of samples, (ii) introducing a flexible statistical modeling framework, including multi-group and time-course analyses and (iii) introducing a new set of data visualizations for expressed region analysis. We apply this approach to public RNA-seq data from the Genotype-Tissue Expression (GTEx) project and BrainSpan project to show that derfinder permits the analysis of hundreds of samples at base resolution in R, identifies expression outside of known gene boundaries and can be used to visualize expressed regions at base-resolution. In simulations, our base resolution approaches enable discovery in the presence of incomplete annotation and is nearly as powerful as feature-level methods when the annotation is complete. derfinder analysis using expressed region-level and single base-level approaches provides a compromise between full transcript reconstruction and feature-level analysis. The package is available from Bioconductor at www.bioconductor.org/packages/derfinder.
| Original language | English (US) |
|---|---|
| Pages (from-to) | e9 |
| Journal | Nucleic acids research |
| Volume | 45 |
| Issue number | 2 |
| DOIs | |
| State | Published - Jan 1 2017 |
| Externally published | Yes |
Funding
The Genotype-Tissue Expression (GTEx) Project was supported by the Common Fund of the Office of the Director of the National Institutes of Health. Additional funds were provided by the NCI, NHGRI, NHLBI, NIDA, NIMH and NINDS. Donors were enrolled at Biospecimen Source Sites funded by NCI/SAIC-Frederick, Inc. (SAIC-F) subcontracts to the National Disease Research Interchange (10XS170), Roswell Park Cancer Institute (10XS171) and Science Care, Inc. (X10S172). The Laboratory, Data Analysis and Coordinating Center (LDACC) was funded through a contract (HHSN268201000029C) to The Broad Institute, Inc. Biorepository operations were funded through an SAIC-F subcontract to Van Andel Institute (10ST1035). Additional data repository and project management were provided by SAIC-F (HHSN261200800001E). The raw data (sequencing reads and phenotype data) used for the analyses described in this manuscript were obtained from SRA accession number phs000424.v6.p1 on 10/07/2015. NIH [1R01GM105705 to J.T.L.]; Consejo Nacional de Ciencia y Tecnología México [351535 to L.C.T.]; A.E.J. was supported by 1R21MH109956.
| Funders | Funder number |
|---|---|
| Broad Institute, Inc. | HHSN261200800001E, 10ST1035 |
| National Disease Research Interchange | 10XS170 |
| SAIC Frederick Inc. | |
| Science Care, Inc. | HHSN268201000029C, X10S172 |
| Author National Institutes of Health National Institutes of Health National Institutes of Health National Institutes of Health The Bev Hartig Huntington's Disease Foundation National Institutes of Health | 1R01GM105705 |
| National Institutes of Health National Institute of Mental Health | R21MH109956 |
| National Institute on Drug Abuse | |
| National Institute of Health National Heart, Lung, and Blood Institute | |
| National Human Genome Research Institute | |
| National Institute of Health-National Cancer Institute | |
| National Institute of Neurological Disorders and Stroke | |
| Roswell Park Alliance Foundation, Roswell Park Cancer Institute | 10XS171 |
| Consejo Nacional de Ciencia y Tecnología - Paraguay | 1R21MH109956, 351535 |
ASJC Scopus subject areas
- Genetics
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