Can you point me to the paper where they describe the method used for peak calling on Broad Institute histone modification chip seq data?
Best regards
Can you point me to the paper where they describe the method used for peak calling on Broad Institute histone modification chip seq data?
Best regards
The UCSC information about the Broad/Encode Histone modification track says:
Discrete intervals of ChIP-seq fragment enrichment were identified using Scripture, a scan statistics approach, under the assumption of uniform background signal.
Scripture is available from the Broad Institute Web Page. The citation is doi:10.1038/nbt.1633.
While Scripture looks like software for RNA-Seq analysis, it seems it can be used for ChIP-Seq analysis using the -task chip
flag. It is not clear that there is a paper that directly describes this use of the software.
Ernst, J., Kheradpour, P., Mikkelsen, T., Shoresh, N., Ward, L., Epstein, C., Zhang, X., Wang, L., Issner, R., Coyne, M., Ku, M., Durham, T., Kellis, M., & Bernstein, B. (2011). Mapping and analysis of chromatin state dynamics in nine human cell types Nature DOI: 10.1038/nature09906
http://www.nature.com/nature/journal/v473/n7345/full/nature09906.html
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Interesting, I hadn't realized Scripture was so versatile. The bit about "under the assumption of uniform background signal" sounds a bit dangerous though. I thought it was pretty well established that the background signal is far from uniform.
Thank yo so much! I used scripture on encode h3k4 data, but couldn't reproduce their results completely (e.g. I always get a subset of peaks/regions), so I was hoping they somewhere described the exact parameters used.