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  • azi
    replied
    Hi

    I also use tophat to map RNA-seq data, and I have some questions, does the tag NH:i:1 work for pair-ended reads? Or it just concerns one mate read?

    I mean, if I accept all alignments which have the tag NH:i:1, could I be sure that specific pairs which can be alined only one time, are all selected?

    In other words, is it possible one mate has "NH:i:1", an the other mate has "NH:i:3"?
    Last edited by azi; 12-12-2012, 05:11 AM.

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  • ttnguyen
    replied
    Hope this is not too late to ask a question on this topic.
    Is it the right way to extract unique-reads by just simply basing on the read name in SAM/BAM file (after filtering out reads having no reported alignments, i.e. samtools view -F4) ? It means a read is called unique-mapped if its name occurs exactly one time (for single-end). I asked this because I were afraid that different aligners use different ways to report mapping quality.

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  • nilshomer
    replied
    Mapping quality of zero usually means the mapping could not be unambiguously placed, which is likely in repeat regions.

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  • chenyao
    replied
    I figure out: using grep -w or awk.

    Another question : lots of reads (mapping quality=0) are aligned to reapeted region in my RNA-seq data. what does this mean?

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  • chenyao
    replied
    Originally posted by nilshomer View Post
    What is the alignment score (AS tag) for those mapq = 0 reads? Can you post one record?
    After checking the results, I found using grep "XH:i:1" I mistook the reads with "XH:i:1**", see the example:

    2045_1360_1504_F5-BC 409 chr7 3155885 0 25M * 0 0 AAAAGGGGGAAGGGAAAGAGGGAGG 004DI:.""-,*"'/);LRYMDNCC NM:i:0 NH:i:10CC:Z:= CP:i:70303403 XS:A:+ HI:i:8


    So what is the script which I can extract "XH:i:1" ?

    Leave a comment:


  • nilshomer
    replied
    What is the alignment score (AS tag) for those mapq = 0 reads? Can you post one record?

    Leave a comment:


  • Question on mapping quality and uniquely mapped read

    Dear all.

    I use tophat to map RNA-seq data. After getting results, I use two ways to filter the alignment. one is using grep "NH:i:1" to get uniquely mapping reads; the other is using samtools view -bq to get reliable reads. However, I found many uniquely mapped reads have mapping quality =0. How to explain it?
    It's a single-end data.

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