Hello ,
I'm dealing with a ChIP-seq data of H3K4me3 modification from drosophila and make a heatmap by deeptools-3.3.0 with following commonds
First, I extract the chromosome number, chrStart, chrEnd, 6, strand and 8 columns from annotated information to make a BED file for computeMatrix
cat dmel-all-r6.19.gtf |awk 'BEGIN{OFS="\t"} {if ($3=="gene") print "chr"$1,$4,$5,$6,$7,$8}'>dm_genes.gtf
Then I use --referencePoint TSS mode and +/-2k as promoter region for computeMatrix and plot the heatmap
computeMatrix reference-point -S 3-11.scale.bw -R dm_genes.gtf -o signal_heatmap/3-11_gtf.gz --referencePoint TSS -a 2000 -b 2000 --skipZeros --missingDataAsZero -p 16
plotHeatmap -m signal_heatmap/3-11_gtf.gz -out signal_heatmap/3-11_gtf.png --colorList white,steelblue --sortUsing max
The resulting plot is as follows:

There is a gap in TSS, which I consider is not that common for H3K4me3 modification at TSS. I'm quite new for ChIP-seq analysis as well as epigentic study of histone modification, so I want to know whether I create the heatmap properly, specificly for how I treat the promoter region.
Any help would be appreciated,
Thanks!
chip-seq