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  • how do you normalize MBD sequencing data?

    Are there tools to normalize read count or find peaks with MBD sequencing data ?

    or Any suggestion for doing that?

    Thank you.

  • #2
    Take the number of mapped reads in your sample and divide it by the number of mapped reads in your control. Use this result to normalized your read data.

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    • #3
      Thank you.

      But what if I do not have input data but comparative data like tumor vs normal?

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      • #4
        do you expect copy number variations?

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