期刊
IEEE-ACM TRANSACTIONS ON COMPUTATIONAL BIOLOGY AND BIOINFORMATICS
卷 14, 期 5, 页码 1070-1081出版社
IEEE COMPUTER SOC
DOI: 10.1109/TCBB.2016.2520919
关键词
GRO-seq; nascent transcription; logisitic regression; hidden Markov models; algorithms; experimentation
类别
资金
- Boettcher Foundation's Webb-Waring Biomedical Research program
- NSF ABI [DBI-12624L0]
- NIH [N 2T15 LM009451]
- NSF IGERT [1144807]
- BioFrontiers IT [NIH 1S10OD012300]
We present a fast and simple algorithm to detect nascent RNA transcription in global nuclear run-on sequencing (GRO-seq). GRO-seq is a relatively new protocol that captures nascent transcripts from actively engaged polymerase, providing a direct read-out on bona fide transcription. Most traditional assays, such as RNA-seq, measure steady state RNA levels which are affected by transcription, post-transcriptional processing, and RNA stability. GRO-seq data, however, presents unique analysis challenges that are only beginning to be addressed. Here, we describe a new algorithm, Fast Read Stitcher (FStitch), that takes advantage of two popular machine-learning techniques, hidden Markov models and logistic regression, to classify which regions of the genome are transcribed. Given a small user-defined training set, our algorithm is accurate, robust to varying read depth, annotation agnostic, and fast. Analysis of GRO-seq data without a priori need for annotation uncovers surprising new insights into several aspects of the transcription process.
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