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  • dpryan
    replied
    You could also just use bamCoverage from deepTools, which handles spliced reads as well.

    Leave a comment:


  • aleferna
    replied
    Another alternative

    For RNA seq data (which has intron spanning reads) I made the following script which:
    1. Does not report coverage over introns.
    2. Generates one file for each strand
    3. Summarized data in 10 bp bins
    4. Does not report bins with less than 3 reads.


    here $bam is the full bam file and $base is the shorted sample name.

    samtools mpileup -d 100000 -q 10 --rf "REVERSE" --ff "UNMAP,SECONDARY,QCFAIL,DUP" $bam | awk -F '\t' '{
    curbin = "chr"$1"\t"int($2/10)*10"\t"int($2/10)*10+10
    if (curbin != lastbin ){
    if (tot/cts > 3){
    print lastbin"\t"tot/cts*-1;
    }
    cts=0;
    tot=0;
    lastbin = curbin
    }
    a=$5
    gsub(/<|>/,"",a)
    a=$4 - length($5) + length(a)
    cts = cts + 1;
    tot = tot + a
    }' > washu/bg/$base.Rev.bedGraph &

    samtools mpileup -d 100000 -q 10 --ff "REVERSE,UNMAP,SECONDARY,QCFAIL,DUP" $bam | awk -F '\t' '{
    curbin = "chr"$1"\t"int($2/10)*10"\t"int($2/10)*10+10
    if (curbin != lastbin ){
    if (tot/cts > 3){
    print lastbin"\t"tot/cts;
    }
    cts=0;
    tot=0;
    lastbin = curbin
    }
    a=$5
    gsub(/<|>/,"",a)
    a=$4 - length($5) + length(a)
    cts = cts + 1;
    tot = tot + a
    }' > washu/bg/$base.For.bedGraph &

    Leave a comment:


  • gokhulkrishnakilaru
    replied
    Thank you all.

    Will give a try and shall let u know.

    Leave a comment:


  • GW_OK
    replied
    I use a combo of samtools, bedtools, and UCSC scripts with a few steps in between to remove chimeras:
    samtools sort -n file.bam file_name_sorted
    samtools view -uf 0x2 ./file_name_sorted.bam | bamToBed -i stdin -bedpe > file.bedpe
    awk '$1 == $4' file.bedpe | awk '{OFS="\t"; print $1, $2, $6, $7}' | sort -k 1,1 > file.bed
    genomeCoverageBed -i file.bed -g hg19.genome -bg > file_name_sorted.cov
    bedGraphToBigWig file_name_sorted.cov hg19.genome file.bw

    Leave a comment:


  • Richard Finney
    replied
    What's needed is "samtools depth" combined with "UCSC wigToBigWig" (that doesn't use 32 GB of memory.)

    Leave a comment:


  • maubp
    replied
    I use this: http://github.com/chapmanb/bcbb/blob...m_to_wiggle.py

    See also http://biostar.stackexchange.com/que...-sam-to-wiggle and Google.

    Leave a comment:


  • gokhulkrishnakilaru
    started a topic Bam to bigwig

    Bam to bigwig

    Hi,

    I have a bunch of sorted bam files and would like to get them converted into bigwig files. Any ideas are highly appreciated.

    Thanks in advance.

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