Schema for R-Loop DRIP-Seq (S2) - R-Loop DRIP-Seq in S2 Cells
  Database: dm6    Primary Table: CSE99014_dH1_RNH1_treated_peakzilla    Row Count: 1,711   Data last updated: 2021-09-01
fieldexampleSQL type info
bin 585smallint(5) unsigned range
chrom chr2Lvarchar(255) values
chromStart 106116int(10) unsigned range
chromEnd 106342int(10) unsigned range
name peakzilla_3306varchar(255) values
score 1int(10) unsigned range
strand .char(1) values
signalValue 2.24float range
pValue -1float range
qValue 0.73353float range
peak 113int(11) range

Sample Rows
 
binchromchromStartchromEndnamescorestrandsignalValuepValueqValuepeak
585chr2L106116106342peakzilla_33061.2.24-10.73353113
587chr2L324917325143peakzilla_3622.4.03-10.7607113
588chr2L505053505279peakzilla_533.2.82-10.6347113
588chr2L505338505564peakzilla_1592.2.57-10.74376113
588chr2L516614516840peakzilla_20791.2.21-10.72033113
589chr2L613215613441peakzilla_36681.2.23-10.72262113
589chr2L626819627045peakzilla_2312.3.8-10.77186113
589chr2L626966627192peakzilla_7641.2.32-10.76145113
590chr2L748891749117peakzilla_43131.2.14-10.7176113
591chr2L844323844549peakzilla_24751.2.22-10.72769113

Note: all start coordinates in our database are 0-based, not 1-based. See explanation here.

R-Loop DRIP-Seq (S2) (rloopDRIPSeq) Track Description
 

Description

These tracks show the putative locations of R-loops based on DRIP-Seq data from Drosophila melanogaster S2 Cells. The samples that were treated with RNase H served as additional controls for identifying R-loops. The regions that are enriched in the DRIP-Seq reads were identified by MACS2 and Peakzilla. The log likelihood ratio evidence tracks were produced by MACS2. The Irreproducible Discovery Rate (IDR) peak calls were produced by the idr program using a global IDR threshold of 0.05.

The DRIP-Seq datasets were obtained from the Gene Expression Omnibus database at NCBI under the accession number GSE99014.

References

Bayona-Feliu A, Casas-Lamesa A, Reina O, Bernués J, Azorin F. Linker histone H1 prevents R-loop accumulation and genome instability in heterochromatin. Nat Commun. 2017 Aug 18;8(1):283.

Bardet AF, Steinmann J, Bafna S, Knoblich JA, Zeitlinger J, Stark A. Identification of transcription factor binding sites from ChIP-seq data at high resolution. Bioinformatics. 2013 Nov 1;29(21):2705-13.

Zhang Y, Liu T, Meyer CA, Eeckhoute J, Johnson DS, Bernstein BE, Nusbaum C, Myers RM, Brown M, Li W, Liu XS. Model-based analysis of ChIP-Seq (MACS). Genome Biol. 2008;9(9):R137.