TY - JOUR
T1 - Computational tools for genome-wide R-loops identification and characterisation
AU - Liu, Rongjie
AU - Gorthi, Aparna
AU - Jin, Yufang
AU - Bishop, Alexander J.R.
AU - Chen, Yidong
N1 - Publisher Copyright:
Copyright © 2017 Inderscience Enterprises Ltd.
PY - 2017
Y1 - 2017
N2 - R-loops are physiologically occurring structures in the genome that composed of a DNA/RNA hybrid and a displaced single-stranded DNA. R-loops have been observed in various organisms and shown to play important roles in regulating gene expression, DNA replication, genome stability, and other functions. The recent introduction of the protocol of DNA-RNA ImmunePrecipitation (DRIP) followed by next-generation sequencing further propels the data accumulation of R-loop formation in different cellular contexts. In this study, we presented a user-friendly tool, DRIPer, for investigating DRIP-seq data to compare against a collection of publicly available DRIP-seq data and ENCODE ChIP-seq. Such comparisons allow correlation analysis and Kolmogorov-Smirnov tests to study associations via a given gene set, which could be for specific biological pathways, ontological functions, or other coregulated genes. This powerful method will enable biologists to quickly evaluate the relationship of R-loops to nearby binding protein sites and target gene expression.
AB - R-loops are physiologically occurring structures in the genome that composed of a DNA/RNA hybrid and a displaced single-stranded DNA. R-loops have been observed in various organisms and shown to play important roles in regulating gene expression, DNA replication, genome stability, and other functions. The recent introduction of the protocol of DNA-RNA ImmunePrecipitation (DRIP) followed by next-generation sequencing further propels the data accumulation of R-loop formation in different cellular contexts. In this study, we presented a user-friendly tool, DRIPer, for investigating DRIP-seq data to compare against a collection of publicly available DRIP-seq data and ENCODE ChIP-seq. Such comparisons allow correlation analysis and Kolmogorov-Smirnov tests to study associations via a given gene set, which could be for specific biological pathways, ontological functions, or other coregulated genes. This powerful method will enable biologists to quickly evaluate the relationship of R-loops to nearby binding protein sites and target gene expression.
KW - Binding protein sites
KW - Biological pathways
KW - ChIP-seq
KW - Co-regulated genes
KW - DNA/RNA hybrid
KW - DRIP-seq
KW - DRIPer
KW - Ontological functions
KW - R-loops
KW - Target gene expression
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U2 - 10.1504/IJCBDD.2017.083883
DO - 10.1504/IJCBDD.2017.083883
M3 - Article
AN - SCOPUS:85018302759
SN - 1756-0756
VL - 10
SP - 123
EP - 136
JO - International Journal of Computational Biology and Drug Design
JF - International Journal of Computational Biology and Drug Design
IS - 2
ER -