Unconfigured Ad

Collapse
X
 
  • Time
  • Show
Clear All
new posts
  • JQL
    Member
    • Apr 2011
    • 83

    #1

    sequencing QC and metagenomics

    Hi,

    I just started my first metagenomics shot-gun sequencing analysis. I hope I can get some advice here.

    1. QC process: I am looking at removing duplicate sequences and trimming low quality bases, according to this HMP's SOP. Is this adequate? What is considered a good QC practice?

    2. Data analysis: I am first trying MetaPhlAn by Huttenhower's group. Is there any 'standard' procedure/workflow that this community recommends?

    Thanks for your help,
    John
  • fanli
    Senior Member
    • Jul 2014
    • 197

    #2
    Originally posted by JQL View Post
    1. QC process: I am looking at removing duplicate sequences and trimming low quality bases, according to this HMP's SOP. Is this adequate? What is considered a good QC practice?
    You may want to remove human/host DNA as well. kneaddata from Curtis Huttonhower's group does this, but uses bowtie2's --un-conc output to filter reads, which misses repetitive DNA that doesn't align concordantly. We've taken to manually filtering any read pair that aligns in any fashion to the human reference.

    Originally posted by JQL View Post
    2. Data analysis: I am first trying MetaPhlAn by Huttenhower's group. Is there any 'standard' procedure/workflow that this community recommends?
    There are also k-mer based approaches (e.g. kraken and CLARK) that were recently shown to outperform MetaPhlAn: see here. Generally speaking, I don't think shotgun is as well figured out as 16S, so there is still some exploring to do. You may also be interested in PanPhlAn, ConStrains, etc. that do strain-level profiling.

    We've just gotten into shotgun too, so happy to share any advice.

    Comment

    • JQL
      Member
      • Apr 2011
      • 83

      #3
      Thank you very much for your reply. At this point, any thing will help me get started.

      have a nice weekend,
      John

      Originally posted by fanli View Post
      You may want to remove human/host DNA as well. kneaddata from Curtis Huttonhower's group does this, but uses bowtie2's --un-conc output to filter reads, which misses repetitive DNA that doesn't align concordantly. We've taken to manually filtering any read pair that aligns in any fashion to the human reference.



      There are also k-mer based approaches (e.g. kraken and CLARK) that were recently shown to outperform MetaPhlAn: see here. Generally speaking, I don't think shotgun is as well figured out as 16S, so there is still some exploring to do. You may also be interested in PanPhlAn, ConStrains, etc. that do strain-level profiling.

      We've just gotten into shotgun too, so happy to share any advice.

      Comment

      • bastianwur
        Member
        • Feb 2014
        • 98

        #4
        Other things you'll need to do:
        - assembly, best cross-assembly if you have multiple samples
        - genomic binning (e.g. maxBin)
        - gene prediction (prodigal has a setting for meta, but only bacteria; ncRNAs can be predicted with rnammer, trnascan-SE and rfam)
        - function prediction (via KO, InterproScan, PRIAM, dbCAN, etc)

        Comment

        Latest Articles

        Collapse

        • SEQadmin2
          Beyond CRISPR/Cas9: Understand, Choose, and Use the Right Genome Editing Tool
          by SEQadmin2



          CRISPR/Cas9 sparked the gene editing revolution for both research and therapeutics.1 But this system still showed severe issues that limited its applications. The most prominent were the heavy reliance on PAM sequences, delivery limitations, double-stranded breaks that prompt unintended edits and cell death, and editing inefficiency (both in targeting and in knock-in reliability).

          Despite this, “CRISPR helped turn genome editing from a specialized technique into
          ...
          07-31-2026, 11:01 AM
        • SEQadmin2
          Proteomic Platforms: How to Choose the Right Analytical Strategy to Improve Detection and Clinical Applications
          by SEQadmin2


          Proteomics platforms are evolving rapidly, with advances in mass spectrometry and affinity-based approaches expanding what researchers can detect and at what scale. As the field moves toward deeper proteome coverage and clinical applications, scientists face an increasingly complex landscape of tools. This article will explore how researchers are navigating these choices to find the right platform for their work.

          The systematic characterization of the human proteome has
          ...
          07-20-2026, 11:48 AM

        ad_right_rmr

        Collapse

        News

        Collapse

        Topics Statistics Last Post
        Started by SEQadmin2, Yesterday, 10:05 AM
        0 responses
        8 views
        0 reactions
        Last Post SEQadmin2  
        Started by SEQadmin2, 08-13-2026, 12:22 PM
        0 responses
        33 views
        0 reactions
        Last Post SEQadmin2  
        Started by SEQadmin2, 08-11-2026, 10:35 AM
        0 responses
        27 views
        0 reactions
        Last Post SEQadmin2  
        Started by SEQadmin2, 08-06-2026, 07:41 AM
        0 responses
        38 views
        0 reactions
        Last Post SEQadmin2  
        Working...