Unconfigured Ad

Collapse
X
 
  • Time
  • Show
Clear All
new posts
  • mzpitman
    Junior Member
    • May 2011
    • 7

    #1

    QC of NGS analysis pipeline?

    Sorry if this is a noob question, but how do you currently QC your NGS analysis workflow? - i.e. generate simulated data with known variants, then compare how your pipeline performed against known data... What are ways that you have set up a QC for your analysis workflow, pitfalls to avoid, etc.
  • adaptivegenome
    Super Moderator
    • Nov 2009
    • 436

    #2
    Your best bet is to start with GATK Best Practices...

    Comment

    • mzpitman
      Junior Member
      • May 2011
      • 7

      #3
      Originally posted by genericforms View Post
      Your best bet is to start with GATK Best Practices...
      Thanks for this - it looks like a good start, but I was wondering about specifically simulating data from different sequencers that mimics real data - like a region of interest - so that you can QC how your pipeline would react to different data types, maybe decide which sequencer would be best for a particular experiment...

      Comment

      • adaptivegenome
        Super Moderator
        • Nov 2009
        • 436

        #4
        Originally posted by mzpitman View Post
        Thanks for this - it looks like a good start, but I was wondering about specifically simulating data from different sequencers that mimics real data - like a region of interest - so that you can QC how your pipeline would react to different data types, maybe decide which sequencer would be best for a particular experiment...
        This is of broad interest to many on this board. I don't have simple answer for you but I agree this should be an area of focus for all of us.

        Comment

        • turnersd
          Senior Member
          • May 2011
          • 115

          #5
          Originally posted by genericforms View Post
          This is of broad interest to many on this board. I don't have simple answer for you but I agree this should be an area of focus for all of us.
          I agree. I hope this discussion continues.

          What sort of NGS application are you considering? DNA? RNA-seq? ChIP-seq? Methylation?

          Perhaps this would make for a good how to wiki page - techniques and software for pre- and post- alignment and assembly quality assessment / quality control.

          Comment

          • mzpitman
            Junior Member
            • May 2011
            • 7

            #6
            Originally posted by genericforms View Post
            This is of broad interest to many on this board. I don't have simple answer for you but I agree this should be an area of focus for all of us.
            Thanks, that validates that at least I'm thinking in the right direction... I'm working on some tools for this type of analysis QC/data simulation. So, I'll let everybody know when I have something to try.

            Still open to pointers from anyone who has tried something similar...

            Comment

            • mzpitman
              Junior Member
              • May 2011
              • 7

              #7
              Originally posted by turnersd View Post
              I agree. I hope this discussion continues.

              What sort of NGS application are you considering? DNA? RNA-seq? ChIP-seq? Methylation?

              Perhaps this would make for a good how to wiki page - techniques and software for pre- and post- alignment and assembly quality assessment / quality control.
              So, at the moment I have mostly DNA data, but I'm also working on 1 RNA-seq project and 1 ChIP-Seq project as well.

              I think a wiki page would be very cool for this, but the discussion needs to progress further. At this point this is mostly just an idea I have in my head a few hacked py scripts that aren't doing what they're told to, and some interest on this forum.

              I hope this discussion does keep going because I think analysis QC is easily overlooked, but necessary - even critical in some settings.

              Comment

              • Alex Renwick
                Member
                • Jul 2011
                • 44

                #8
                Originally posted by mzpitman View Post
                ...
                Still open to pointers from anyone who has tried something similar...
                You might start with wgsim for read simulation. It's purpose is more for assessing mapper accuracy than evaluating the whole analysis pipeline. Sequencing errors are limited to substitutions (no indels), and insertion variants are of limited length. But it's small and fast and reliable for what it does.

                Comment

                • mzpitman
                  Junior Member
                  • May 2011
                  • 7

                  #9
                  Originally posted by Alex Renwick View Post
                  You might start with wgsim for read simulation. It's purpose is more for assessing mapper accuracy than evaluating the whole analysis pipeline. Sequencing errors are limited to substitutions (no indels), and insertion variants are of limited length. But it's small and fast and reliable for what it does.
                  Thanks. I'd seen this before, but it was a good reminder because I'd forgotten about it.

                  Comment

                  Latest Articles

                  Collapse

                  • SEQadmin2
                    16S/ITS Profiling vs. Shotgun Metagenomics: What Changes in Your Workflow?
                    by SEQadmin2




                    NGS has revolutionized clinical microbiology by offering new ways to identify and surveil pathogens without prior knowledge of the target. One popular approach is 16S rRNA and ITS amplicon sequencing, which targets specific microbial markers. But studies are increasingly incorporating shotgun metagenomics, a technique that sequences all DNA from a sample without targeting specific microbial markers. This approach allows more detailed taxonomic classification, detection...
                    Today, 06:46 AM
                  • SEQadmin2
                    Multiomic Liquid Biopsy: What DNA/RNA Panels Reveal That DNA Alone Can’t
                    by SEQadmin2



                    Tumors contain complex mixtures of cell populations that evolve in response to treatment and host-specific factors. Tissue biopsies provide only static snapshots of a tumor’s state. But what if we could follow that evolution over time using a minimally invasive technique?

                    Liquid biopsies can detect tumor-derived material circulating in the bloodstream, providing a way to study treatment response, detect emerging resistance, and discover new biomarkers. Circulating
                    ...
                    10-14-2026, 09:55 AM

                  ad_right_rmr

                  Collapse

                  News

                  Collapse

                  Topics Statistics Last Post
                  Started by SEQadmin2, 10-28-2026, 09:57 AM
                  0 responses
                  24 views
                  0 reactions
                  Last Post SEQadmin2  
                  Started by SEQadmin2, 10-28-2026, 09:51 AM
                  0 responses
                  15 views
                  0 reactions
                  Last Post SEQadmin2  
                  Started by SEQadmin2, 10-22-2026, 11:13 AM
                  0 responses
                  68 views
                  0 reactions
                  Last Post SEQadmin2  
                  Started by SEQadmin2, 10-22-2026, 10:48 AM
                  0 responses
                  48 views
                  0 reactions
                  Last Post SEQadmin2  
                  Working...