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  • nilshomer
    Nils Homer
    • Nov 2008
    • 1283

    #1

    Sequence Alignment Quality Control

    As manual processing of sequencing data becomes impossible, it would be good to identify sequencing quality metrics that could/should be calculated/plotted within a sequencing pipeline.

    What programs do you use to check the quality of your sequencing runs? Specifically, what metrics have you found useful pre-alignment, post-alignment, and post-variant-detection? What metrics/plots would you find useful if they were automatically generated?
  • drio
    Senior Member
    • Oct 2008
    • 323

    #2
    Originally posted by nilshomer View Post
    As manual processing of sequencing data becomes impossible, it would be good to identify sequencing quality metrics that could/should be calculated/plotted within a sequencing pipeline.

    What programs do you use to check the quality of your sequencing runs? Specifically, what metrics have you found useful pre-alignment, post-alignment, and post-variant-detection? What metrics/plots would you find useful if they were automatically generated?
    Here are some that come to my mind:

    Pre-alignment:

    1. Assuming we have available genotype data on the sample, some quick screening of the reads to find genotype concordance can be useful to avoid sample swaps.

    Post-alignment:

    1. Basic stats: % mapped uniquely mapped reads, % mapped reads, effective %mapped reads (after removing PCR duplicates), total throughput, effective throughput (after removing duplicates).

    2. Error rate plot. For CS, before and after CS corrections.

    3. For MP data: insert size distribution plot.

    Post variant detection:

    1. plot: ref/var coverage distribution.

    Nils, which ones are you using on your end? Anyone?
    -drd

    Comment

    • nilshomer
      Nils Homer
      • Nov 2008
      • 1283

      #3
      Originally posted by drio View Post
      Here are some that come to my mind:

      Pre-alignment:

      1. Assuming we have available genotype data on the sample, some quick screening of the reads to find genotype concordance can be useful to avoid sample swaps.

      Post-alignment:

      1. Basic stats: % mapped uniquely mapped reads, % mapped reads, effective %mapped reads (after removing PCR duplicates), total throughput, effective throughput (after removing duplicates).

      2. Error rate plot. For CS, before and after CS corrections.

      3. For MP data: insert size distribution plot.

      Post variant detection:

      1. plot: ref/var coverage distribution.

      Nils, which ones are you using on your end? Anyone?
      I have few those above implemented and more but I want to get a reasonable group of QC metrics before releasing. How would you compare genotypes before alignment? Would you look for specific sequences?

      Comment

      • Chipper
        Senior Member
        • Mar 2008
        • 323

        #4
        Post alignment: compare enrichment / read distributions for different fractions of reads (high quality vs low quality, number of mismatches for reads in ChIP-seq peaks etc). Bin reads by average QV and compare % aligned reads for different aligners at different QV. For comparison between aligners I would also look at differences in coverage over various repeats, what % reads are uniquely placed by only one aligner and how many reads are placed at different positions.

        Comment

        • nilshomer
          Nils Homer
          • Nov 2008
          • 1283

          #5
          Originally posted by Chipper View Post
          Post alignment: compare enrichment / read distributions for different fractions of reads (high quality vs low quality, number of mismatches for reads in ChIP-seq peaks etc). Bin reads by average QV and compare % aligned reads for different aligners at different QV. For comparison between aligners I would also look at differences in coverage over various repeats, what % reads are uniquely placed by only one aligner and how many reads are placed at different positions.
          I do not mean to compare aligners, but evaluate the alignment itself.

          Comment

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