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  • Frequency of A, C, T, or G at every position in SAM file

    Dear all,

    We would like to extract the read depth of each base type (A, C, T or G) for every position of our aligned reads (a SAM file created using Bowtie2).

    Does anyone know of a tool that does this?

    The closest link I found here was:
    Discussion of next-gen sequencing related bioinformatics: resources, algorithms, open source efforts, etc


    But I'm not sure that would be appropriate for use with aligned genome data.

    Many thanks

  • #2
    Hi- I think pysamstats can do what you need.

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    • #3
      Dear dariober,

      We've got pysamstats up and running and it seems to be generating exactly the kind of output we require!

      Many thanks for your help, Matt

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