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  • Evaluating the necessity of PCR duplicate removal from next-generation sequencing

    data and a comparison of approaches

     

    Authors: Mark Ebbert*, Mark Wadsworth*, Lyndsay Staley*, Kaitlyn Hoyt, Brandon Pickett, Justin Miller, John Duce, for the Alzheimer's Disease Neuroimaging Initiative, John SK Kauwe, Perry Ridge

     

    BMC Bioinformatics

    Article

    20 Citations

    July, 2016

    Above Average Altmetric Score of 3

        Tweeted by 5 people

        130 Mendeley Readers

     

  • Novelty of Approach

     

    -Evaluated PCR duplicate removal on final genome assembly

    -Compared CHIP seq data with whole genome sequencing (WGS) data

    -Performed depth of coverage analysis on WGS data

     

  • Results

     

    -92 % of the 17+ million variants called were called whether we removed duplicates with Picard or SAMTools, or left the PCR duplicates in the dataset.

    -No significant differences between the unique variant sets

     

  • Implications

     

    -Removing PCR duplicates is unnecessary

    -Save compute and analysis time by not removing PCR duplicates