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Updated: May 25, 2025

CARIP-Seq and ChIP-Seq: Methods to Identify Chromatin-Associated RNAs and Protein-DNA Interactions in Embryonic Stem Cells
Published on: May 25, 2018
Comprehensive analysis of RNA-chromatin, RNA-, and DNA-protein interactions
Daniil A Khlebnikov1,2, Arina I Nikolskaya2, Anastasia A Zharikova1,2,3
1RTC Bioinformatics, Kharkevich Institute for Information Transmission Problems of RAS, Bolshoy Karetny per. 19, build.1, 127051 Moscow, Russia.
Abstract:
RNA-chromatin interactome data are considered to be one of the noisiest types of data in biology. This is due to protein-coding RNA contacts and nonspecific interactions between RNA and chromatin caused by protocol specifics. Therefore, finding regulatory interactions between certain transcripts and genome loci requires a wide range of filtering techniques to obtain significant results. Using data on pairwise interactions between these molecules, we propose a concept of triad interaction involving RNA, protein, and a DNA locus. The constructed triads show significantly less noise contacts and are more significant when compared to a background model for generating pairwise interactions. RNA-chromatin contacts data can be used to validate the proposed triad object as positive (Red-ChIP experiment) or negative (RADICL-seq NPM) controls. Our approach also filters RNA-chromatin contacts in chromatin regions associated with protein functions based on ChromHMM annotation.
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