Quality control of Chip-seq data (NRF and PCB)

Hi, I'm checking my ChIP-seq library, and I'm following ENCODE guidelines but I can't figure out whether NRF and PCB analysis should be done before or after removing PCR duplicates or before. I know this is probably a stupid question but I just can't figure it out.

Thank you

control library quality pcb chip-seq nrf

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updated 3.6 years ago by Joda 0 • | written 3.6 years ago by michelafrancesconi9 3

If you remove the duplicates then the non-redundant/non-duplicated fraction will be 1.0. But if you save the log file during the de-duplication then you will get the number of replicates.

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written 3.6 years ago by Darked89 469

Can you explain me better? Because for the NRF I do :

a) samtools view -c .bam b)samtools view -c -F 260 .bam

then b/a

and as a bam file I use the one that I deduplicate

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written 3.6 years ago by michelafrancesconi9 3

If you use samtools markdup then samtools markdup -r -f foo.log foo.bam foo.dedup.bam should give you deduplicated BAM and duplication stats. Does it answer your question?

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written 3.6 years ago by Darked89 469

Not really, because I already have deduplicate my bam file so I already know the number of deduplicate reads. I have a bam file that is without the deduplication (my final bam) and a bam file that keep it. My question is how calculate NRF now that I have the two files.

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written 3.6 years ago by michelafrancesconi9 3

Any resolution? im struggling with the same problems for obtaining the NRF if it works , I used this for calculating PBC.

PBC <- function(IP) {

require(GenomicAlignments)
require(data.table)

# load ChIP sample if necessary
if (is.character(IP)) {
    if (!file.exists(IP))
        stop(paste("File", IP, "does NOT exist."))
    else
        aln <- readGAlignments(IP)
} else if (class(IP) == "GAlignments") {
    aln <- IP
} else {
    stop("IP must be a file path or a GAlignments object.")
}

# convert GAlignments object to data.table for fast aggregation
aln <- data.table(
    strand=as.factor(BiocGenerics::as.vector(strand(aln))),
    seqnames=as.factor(BiocGenerics::as.vector(seqnames(aln))),
    pos=ifelse(strand(aln) == "+", start(aln), end(aln))
)

# aggregate reads by position and count them
readsPerPosition <- aln[,list(count=.N), by=list(strand, seqnames, pos)]$count

# PBC = positions with exactly 1 read / positions with at least 1 read
PBC <- sum(readsPerPosition == 1) / length(readsPerPosition)

return(PBC)

} an then use this... PBC(your-bam.bam)

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written 3.6 years ago by Joda 0

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