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DROPA: DRIP-seq optimized peak annotator.


ABSTRACT: BACKGROUND:R-loops are three-stranded nucleic acid structures that usually form during transcription and that may lead to gene regulation or genome instability. DRIP (DNA:RNA Immunoprecipitation)-seq techniques are widely used to map R-loops genome-wide providing insights into R-loop biology. However, annotation of DRIP-seq peaks to genes can be a tricky step, due to the lack of strand information when using the common basic DRIP technique. RESULTS:Here, we introduce DRIP-seq Optimized Peak Annotator (DROPA), a new tool for gene annotation of R-loop peaks based on gene expression information. DROPA allows a full customization of annotation options, ranging from the choice of reference datasets to gene feature definitions. DROPA allows to assign R-loop peaks to the DNA template strand in gene body with a false positive rate of less than 7%. A comparison of DROPA performance with three widely used annotation tools show that it identifies less false positive annotations than the others. CONCLUSIONS:DROPA is a fully customizable peak-annotation tool optimized for co-transcriptional DRIP-seq peaks, which allows a finest gene annotation based on gene expression information. Its output can easily be integrated into pipelines to perform downstream analyses, while useful and informative summary plots and statistical enrichment tests can be produced.

SUBMITTER: Russo M 

PROVIDER: S-EPMC6685255 | biostudies-literature | 2019 Aug

REPOSITORIES: biostudies-literature

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DROPA: DRIP-seq optimized peak annotator.

Russo Marco M   De Lucca Bruno B   Flati Tiziano T   Gioiosa Silvia S   Chillemi Giovanni G   Capranico Giovanni G  

BMC bioinformatics 20190806 1


<h4>Background</h4>R-loops are three-stranded nucleic acid structures that usually form during transcription and that may lead to gene regulation or genome instability. DRIP (DNA:RNA Immunoprecipitation)-seq techniques are widely used to map R-loops genome-wide providing insights into R-loop biology. However, annotation of DRIP-seq peaks to genes can be a tricky step, due to the lack of strand information when using the common basic DRIP technique.<h4>Results</h4>Here, we introduce DRIP-seq Opti  ...[more]

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