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  • sequencingfan
    Member
    • Feb 2014
    • 13

    #1

    PCR duplicates

    Hello,

    what is PCR duplicate in NGS sequencing? Is there a detailed explanation of this problem? What is the impact of PCR duplictes to data analysis.
  • jlei_face
    Member
    • Oct 2014
    • 10

    #2
    Here's a good link:

    Comment

    • sequencingfan
      Member
      • Feb 2014
      • 13

      #3
      What about applications in which we use only Pcr to prepare libraries ( 16 s metagenomics,ion torrent ampliseq etc.).in my opinion most of reads for target region will start and end in the same positions.how to calculate real level of pcr duplication?

      Comment

      • Zaag
        Senior Member
        • Nov 2009
        • 112

        #4
        Originally posted by sequencingfan View Post
        What about applications in which we use only Pcr to prepare libraries ( 16 s metagenomics,ion torrent ampliseq etc.).in my opinion most of reads for target region will start and end in the same positions.how to calculate real level of pcr duplication?
        If you are building an amplicon library you will only have PCR duplicates, so you leave them in. If you build a shotgun library you'll want to remove them.

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