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  • ramouz87
    Member
    • Oct 2009
    • 35

    #1

    how to get perfects aligned reads instead of real read

    Hi,
    Is there any way to modify a SAM/BAM in order to have real reads replaced by the perfect reads(replacing wrong bases with the right bases in the ref) ?
    for example:
    REF : ACTGTGTCCTGTACTG
    READ: TCTGTGTCCTTTACTG

    the REF sequence will be showed instead of the real read.

    One solution is to fetch the postion of each read(chr:start-end) and fetch the proprer reads from the reference but i'm wondering if there's a better way to do that directely using samtools/awk ?
    The desired output is bam or fastq
    Thanks in advance
    Best,
    Ramzi
    Research Scientist - Bioinformatics
    Sidra Medical and Research Center
  • nilshomer
    Nils Homer
    • Nov 2008
    • 1283

    #2
    Originally posted by ramouz87 View Post
    Hi,
    Is there any way to modify a SAM/BAM in order to have real reads replaced by the perfect reads(replacing wrong bases with the right bases in the ref) ?
    for example:
    REF : ACTGTGTCCTGTACTG
    READ: TCTGTGTCCTTTACTG

    the REF sequence will be showed instead of the real read.

    One solution is to fetch the postion of each read(chr:start-end) and fetch the proprer reads from the reference but i'm wondering if there's a better way to do that directely using samtools/awk ?
    The desired output is bam or fastq
    Thanks in advance
    Best,
    Ramzi
    Use the cigar field and the MD tag (if available) to convert the read into the reference without having to search a reference FASTA file. I will leave it to you as an exercise, though you can checkout the bio-samtools (written in perl).

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