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  • Software genome align and mutation finder

    Hi, I have 2 bacterial genomes (wt and mut) sequenced.

    I've already assembled the genomes with velvet and mauve.

    What I need now is a software that let me to align them and easily (and possibly with a graphical interface, since then It should also be used by non-bioinformatician) identify the presence of point mutation, deletions and insertions.


    Any ideas?

  • #2
    Is there anyone that can help me??

    Comment


    • #3
      If you want to identify mutations, you can map the reads of the mutant to the wild-type assembly and call variants with a variant caller. For example, with the BBMap package:

      Code:
      bbmap.sh in=mut_reads.fq ref=wt_assembly.fasta out=mapped.sam bs=bs.sh
      
      callvariants.sh in=mapped.sam ref=wt_assembly.fasta vcf=variants.vcf
      Then the variants are in the variants.vcf file, which is fairly easy to read. You can look at the variants visually in a program like IGV using the sorted, indexed bam file, which can be produced by running the shell script bs.sh that gets created by BBMap.
      Last edited by Brian Bushnell; 12-20-2016, 10:24 AM.

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      • #4
        Thaks a lot. I'll try this way

        Comment

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