Unconfigured Ad

Collapse
X
 
  • Time
  • Show
Clear All
new posts
  • feralBiologist
    Member
    • Jun 2011
    • 61

    #1

    Comparative bacterial genomics on groups of samples

    Here is my project:

    - I have a group X of unknown strains of species A taken from, say, the oral cavities of a group of people. Each individual gives rise to a single sample. The bacterial species is cultured and then sequenced on MiSeq.

    - Similarly to above I have a group of unknown strains Y of the same species but taken from another body compartment - say the gut. This may (or may not) be the same people as above.

    The task is to find whether there is anything that systematically differs between the first and the second group.

    I was first thinking of picking a reference and than doing alignment for each sample. But this poses the problem of picking the right reference. As we have dozens of samples this may not even be the same reference. Is there a way to compare the samples as groups so that we were able to check whether there are any

    - systematic difference in gene presence (e.g. group X has a gene that is not present in group Y)

    - systematic difference in genes that are present in both groups (e.g. gene B has a particular SNP/indel in group X but not in group Y)

    We are, essentially, trying to compare groups. Is there a way to answer these questions on a group level without doing sample level analysis.

    And if we still need to do a sample level analysis do we need to go for de novo assembly or reference-based alignment? Another question is - we have just MiSeq data. Do we need longer reads (e.g. PacBio)?

    Essentially, what we are trying to do is some sort of GWA on bacteria without knowing the sequences of the individual strains. How to best approach this task? Can you suggest a pipeline? Do you know of any papers that have done this?

    ps. I've posted a similar post on biostars but haven't received satisfactory answers.
    Last edited by feralBiologist; 02-11-2016, 02:53 AM.

Latest Articles

Collapse

  • 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
  • SEQadmin2
    New Genomics Technologies Take Aim at Long-Standing Limits
    by SEQadmin2


    Researchers using sequencing and genomics tools often have to make trade-offs. They can choose between speed or scale, short reads or long-range information, or targeted panels or a view of the whole transcriptome. New technologies that have been released this year are built to address those tough choices.

    We asked six companies the same four questions to learn about their latest products. The new technologies bring a lot to the table, including rethinking sequencing
    ...
    09-28-2026, 10:25 AM

ad_right_rmr

Collapse

News

Collapse

Topics Statistics Last Post
Started by SEQadmin2, Yesterday, 11:13 AM
0 responses
18 views
0 reactions
Last Post SEQadmin2  
Started by SEQadmin2, Yesterday, 10:48 AM
0 responses
18 views
0 reactions
Last Post SEQadmin2  
Started by SEQadmin2, 10-15-2026, 10:52 AM
0 responses
36 views
0 reactions
Last Post SEQadmin2  
Started by SEQadmin2, 10-14-2026, 05:39 AM
0 responses
42 views
0 reactions
Last Post SEQadmin2  
Working...