Seqanswers Leaderboard Ad

Collapse

Announcement

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

  • 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

  • #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


    • #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


      • #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

        • seqadmin
          Recent Advances in Sequencing Analysis Tools
          by seqadmin


          The sequencing world is rapidly changing due to declining costs, enhanced accuracies, and the advent of newer, cutting-edge instruments. Equally important to these developments are improvements in sequencing analysis, a process that converts vast amounts of raw data into a comprehensible and meaningful form. This complex task requires expertise and the right analysis tools. In this article, we highlight the progress and innovation in sequencing analysis by reviewing several of the...
          Yesterday, 07:48 AM
        • seqadmin
          Essential Discoveries and Tools in Epitranscriptomics
          by seqadmin




          The field of epigenetics has traditionally concentrated more on DNA and how changes like methylation and phosphorylation of histones impact gene expression and regulation. However, our increased understanding of RNA modifications and their importance in cellular processes has led to a rise in epitranscriptomics research. “Epitranscriptomics brings together the concepts of epigenetics and gene expression,” explained Adrien Leger, PhD, Principal Research Scientist...
          04-22-2024, 07:01 AM

        ad_right_rmr

        Collapse

        News

        Collapse

        Topics Statistics Last Post
        Started by seqadmin, Today, 06:57 AM
        0 responses
        9 views
        0 likes
        Last Post seqadmin  
        Started by seqadmin, Yesterday, 07:17 AM
        0 responses
        13 views
        0 likes
        Last Post seqadmin  
        Started by seqadmin, 05-02-2024, 08:06 AM
        0 responses
        19 views
        0 likes
        Last Post seqadmin  
        Started by seqadmin, 04-30-2024, 12:17 PM
        0 responses
        22 views
        0 likes
        Last Post seqadmin  
        Working...
        X