Unconfigured Ad

Collapse
X
 
  • Filter
  • Time
  • Show
Clear All
new posts
  • mmmm
    Senior Member
    • Jul 2013
    • 131

    SNPs_analysis

    Dear all, I have 2 draft genomes of bacteria assembled by velvet and I used Mauve to extract snps (but I need your advice to:
    - know if these snps are synonomas or nonsynonomas
    -in which genes they are located?

    is there a softwrae that can do this?

    (I know snpeff- can be used but I do not have a reference strain)

    your advice is very appreciated
  • TiborNagy
    Senior Member
    • Mar 2010
    • 329

    #2
    First you need to create an annotation (RAST) and after that you can use snpeff.

    Comment

    • mmmm
      Senior Member
      • Jul 2013
      • 131

      #3
      thanks- have created the annotation using RAST on the draft genome- now how to us the annotation file in snpeff (can I download the genbank file to snpeff database)???

      Comment

      • BurlEarl
        Member
        • Jun 2012
        • 19

        #4
        This is a pain. To add a custom genome to SnpEff you need to add lines to the snpEff.config file. There is good documentation here:



        Under building databases. It is a little picky.

        i added lines to snpEff.config like this:

        #Friend Murine Leukemia Virus
        X02794.genome : FMuLV

        cd PATH/TO/snpEff/data
        mkdir X02794
        cp PATH/TO/GENBANKFILE/genes.gb X02794/genes.gb

        java -jar snpEff.jar build -genbank -v X02794

        I think that is what i did...Anyway, documentation is pretty good. I remember having a problem with my generated .gb file. Turns out there needed to be a couple of spaces after ORIGIN and the sequence.

        good luck
        --Please take everything thing I say with a grain of salt, because, if grad school has taught me anything, it's that I'm an idiot--

        Comment

        Latest Articles

        Collapse

        • SEQadmin2
          Nine Things a Sample Prep Scientist Thinks About Before Sequencing
          by SEQadmin2


          I’m not a sequencing expert. I’m a purification scientist who uses NGS to evaluate workflows my group develops. With this perspective, we think about the sample first and the NGS workflow second. The sequencer is an exceptionally honest reporter, but it can only report on what you give it, so whether you get clean, interpretable data from an NGS workflow is largely determined before you begin.

          Here are nine questions we think about, in roughly the order they matter, before...
          06-18-2026, 07:11 AM
        • SEQadmin2
          From Collection to Sequencing: Why Sample Preparation and Preservation Define Sequencing Data
          by SEQadmin2


          Data variability is still an issue in sequencing technologies despite the advances in reproducibility and accuracy of these platforms. But the problem does not originate in the sequencing itself, but in the previous steps, before the sample reaches the sequencer.


          The first step is collection, followed by preservation and sample preparation for analysis. Most scientists overlook those steps, but not being careful might just be skewing the experiment’s results.
          ...
          06-02-2026, 10:05 AM

        ad_right_rmr

        Collapse

        News

        Collapse

        Topics Statistics Last Post
        Started by SEQadmin2, Today, 11:10 AM
        0 responses
        6 views
        0 reactions
        Last Post SEQadmin2  
        Started by SEQadmin2, 06-17-2026, 06:09 AM
        0 responses
        41 views
        0 reactions
        Last Post SEQadmin2  
        Started by SEQadmin2, 06-09-2026, 11:58 AM
        0 responses
        102 views
        0 reactions
        Last Post SEQadmin2  
        Started by SEQadmin2, 06-05-2026, 10:09 AM
        0 responses
        123 views
        0 reactions
        Last Post SEQadmin2  
        Working...