Seqanswers Leaderboard Ad

Collapse

Announcement

Collapse
No announcement yet.
X
 
  • Filter
  • Time
  • Show
Clear All
new posts

  • Where do NGS projects most often Fail?

    When thinking about a new project, where do you see the most failures?
    1. DNA/RNA extraction
    2. Library Prep
    3. Sequencing Run
    4. Alignment / Assembly
    5. Secondary/Tertiary analysis and BioInformatics

    At what point do you finally feel like a project is "safe"?

  • #2
    I am not sure if this question has a generally applicable answer. Projects can fail at any step mentioned in your list. A project can never be "safe" (to borrow your phrase) until the data is analyzed and the paper written :-)

    Comment


    • #3
      Experimental design: not choosing appropriate controls, too few biological replicates, or doing sequencing on the wrong cell population (e.g. whole-blood RNASeq for an obesity study).

      Comment


      • #4
        Originally posted by gringer View Post
        Experimental design: not choosing appropriate controls, too few biological replicates, or doing sequencing on the wrong cell population (e.g. whole-blood RNASeq for an obesity study).
        This!

        Biggest mistake is too few replicates. Individual samples can drop out for a variety of reasons, so easily your glorious n=3 study has treatments with only 2 replicates in them. And you can not easily repeat the missing samples without having a potential batch effect confounder.

        Also, from my experience as a core lab head, usually it is "**** in, **** out", meaning most library preps / sequencing runs fail because input material was not ideal (but customer wanted to try anyway after being contacted following QC).

        Comment


        • #5
          To second what another poster said.....there is no safe place until you have your data analyzed but the most common problem is garbage in,garbage out. In the core lab I was in, we had similar issues where a customer would insist we use their sub-optimal ample, and the data would commonly be garbage.

          It is worth checking all samples on a Bioanalyzer or Tape Station type instrument to really look at what you are dealing with. The most common issue would be someone using a nanodrop to get a concentration, but upon TS we would find it was less than 50% of what they reported

          Comment

          Latest Articles

          Collapse

          • seqadmin
            Current Approaches to Protein Sequencing
            by seqadmin


            Proteins are often described as the workhorses of the cell, and identifying their sequences is key to understanding their role in biological processes and disease. Currently, the most common technique used to determine protein sequences is mass spectrometry. While still a valuable tool, mass spectrometry faces several limitations and requires a highly experienced scientist familiar with the equipment to operate it. Additionally, other proteomic methods, like affinity assays, are constrained...
            04-04-2024, 04:25 PM
          • seqadmin
            Strategies for Sequencing Challenging Samples
            by seqadmin


            Despite advancements in sequencing platforms and related sample preparation technologies, certain sample types continue to present significant challenges that can compromise sequencing results. Pedro Echave, Senior Manager of the Global Business Segment at Revvity, explained that the success of a sequencing experiment ultimately depends on the amount and integrity of the nucleic acid template (RNA or DNA) obtained from a sample. “The better the quality of the nucleic acid isolated...
            03-22-2024, 06:39 AM

          ad_right_rmr

          Collapse

          News

          Collapse

          Topics Statistics Last Post
          Started by seqadmin, 04-11-2024, 12:08 PM
          0 responses
          17 views
          0 likes
          Last Post seqadmin  
          Started by seqadmin, 04-10-2024, 10:19 PM
          0 responses
          22 views
          0 likes
          Last Post seqadmin  
          Started by seqadmin, 04-10-2024, 09:21 AM
          0 responses
          16 views
          0 likes
          Last Post seqadmin  
          Started by seqadmin, 04-04-2024, 09:00 AM
          0 responses
          46 views
          0 likes
          Last Post seqadmin  
          Working...
          X