Seqanswers Leaderboard Ad

Collapse

Announcement

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

  • Making a in silico mock community

    Hello All!

    I am looking to some microbiome work of fecal samples (16S V4 MiSeq). We are interested in detection a number of specific groups of bacteria in the samples. Specifically E. Coli and different Klebsiella species.

    I would like to know in silico whether we will be able to differentiate between species after we run the sequencing.

    What is the best method for testing whether our V4 sequencing will be able to differentiate to species level? Should I just be doing a bunch of blasting or would making a mock in silico community work best?

    Thanks for any help

    Mark

  • #2
    If you are looking for specific microbial species (or really doing anything with NGS reads), BLAST is not really the best tool. You can calculate abundance by mapping or kmer-matching your sequences to just the set of references of interest.

    And certainly, you should first validate that your approach works on synthetic data before proceeding. That will allow you to quantify true positive, false positive, and false negative rates, which may lead you to adjust your methodology prior to doing any real work.

    For kmer-matching, I recommend Seal (part of the BBMap package), which is fast and easy to use for quantifying sequence expressions levels. For example:

    seal.sh in=reads.fq ref=ecoli.fa,klebsiella1.fa,klebsiella2.fa stats=stats.txt refstats=refstats.txt

    If you generate synthetic reads with errors, and annotate the reads with the name of the organism they came from, you can then objectively calculate the accuracy. Alternatively, if you just want to measure levels of various bacteria, you can generate synthetic reads and mix them in a specific ratio, then evaluate your approach by calculating how closely the output of expression levels matches the ratio of reads you mixed together. That's easier as it does not require parsing the read names.
    Last edited by Brian Bushnell; 09-30-2015, 06:22 PM.

    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
    30 views
    0 likes
    Last Post seqadmin  
    Started by seqadmin, 04-10-2024, 10:19 PM
    0 responses
    32 views
    0 likes
    Last Post seqadmin  
    Started by seqadmin, 04-10-2024, 09:21 AM
    0 responses
    28 views
    0 likes
    Last Post seqadmin  
    Started by seqadmin, 04-04-2024, 09:00 AM
    0 responses
    53 views
    0 likes
    Last Post seqadmin  
    Working...
    X