Schema for Histone Variants ChIP-Seq (S2) - ChIP-Seq of Histone Variants in S2 Cells
  Database: dm6    Primary Table: GSE99004_dH1_H2Av_peakzilla    Row Count: 13,434   Data last updated: 2021-09-01
fieldexampleSQL type info
bin 585smallint(5) unsigned range
chrom chr2Lvarchar(255) values
chromStart 21471int(10) unsigned range
chromEnd 21827int(10) unsigned range
name peakzilla_14976varchar(255) values
score 2int(10) unsigned range
strand .char(1) values
signalValue 2.76float range
pValue -1float range
qValue 0.56575float range
peak 178int(11) range

Sample Rows
 
binchromchromStartchromEndnamescorestrandsignalValuepValueqValuepeak
585chr2L2147121827peakzilla_149762.2.76-10.56575178
585chr2L6652466880peakzilla_93553.2.69-10.95311178
585chr2L6697667332peakzilla_152282.2.04-10.55021178
585chr2L7186672222peakzilla_123602.3.56-10.73189178
585chr2L7279873154peakzilla_121242.2.18-10.74618178
585chr2L7404474400peakzilla_99272.2.75-10.90483178
585chr2L7469175047peakzilla_144632.2.54-10.59397178
585chr2L7676677122peakzilla_178921.2.08-10.44563178
585chr2L7842478780peakzilla_156782.2.56-10.52549178
585chr2L7919979555peakzilla_168112.2.06-10.48386178

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

Histone Variants ChIP-Seq (S2) (variantsChIPSeq) Track Description
 

Description

These tracks show the results of the ChIP-Seq analyses of histone variants from S2 cells. The regions that are enriched in histone variants 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 ChIP-Seq datasets were obtained from the Gene Expression Omnibus database at NCBI under the following accession numbers:

AccessionProteinsReference
GSE99004H2Av, H2Av dH1 RNAiBayona-Feliu A et al., Nat Commun. 2017

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.