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Repetitive element coverage of consensus

I have a consensus sequence for a class of repetitive elements (from repbase) and I want to find out the depth coverage of the real genomic instances (taken from ucsc rmask table) against this consensus sequence. The elements tend to become 5' truncated over evolutionary time, so some instances may be quite short, while some instances are full length. I would like to get out something in the end like a wigg file describing the "depth" of instances at each position in the consensus, but I am not sure how to go about it. Any help is greatly appreciated.

EDIT:

One approach I was considering is to break up my instance sequences into k-mers of say 50bp and then align to the consensus reference via bowtie producing BAM and then using samtools to get the windowed coverage. Thoughts?

chip-seq alignment genome blast
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updated by Ram Ram • written by jmack159 • jmack159

1 answer

I think that its doable

For example :

If you have L1Hs element, (just assuming that this is family of repetitive elements where your consensus belongs)

###### fetch all L1Hs from rmsk_table
grep -wi 'L1Hs' rmsk.bed > L1Hs.bed ### you would get some around 1500 sequences

#### fetch sequences of L1Hs
bedtools getfasta -fi hg19.fa -bed L1Hs.bed -fo L1Hs.fa.out

Now you align your consensus with L1Hs.fa.out

count how many instances are there on every nucleotide resolution. A simple perl script could help or which ever you think is good

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updated by Ram Ram • written by Manvendra Singh Manvendra Singh

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