Unconfigured Ad

Collapse
X
 
  • Time
  • Show
Clear All
new posts
  • id0
    Senior Member
    • Sep 2012
    • 130

    #1

    D. melanogaster known SNPs and indels

    I am working with the fly genome for the first time. I am trying to do realignment and recalibration, which requires known SNPs. Where can I find these (preferably for the UCSC dm3 genome)?

    I found FlySNP (http://flysnp.imp.ac.at/). That seems to be what I am looking for. However, the genome version is not specified and there seems to be no easy way to export the data.

    UCSC does not provide any SNP tracks for the fly like it does for human or mouse, which makes me a little concerned that there is no reliable resource.

    Any insights from someone with D. melanogaster experience would be greatly appreciated.
    Last edited by id0; 08-26-2013, 08:55 AM.
  • aaronh
    Member
    • Sep 2008
    • 46

    #2
    Here are the VCF files from the DGRP: http://www.hgsc.bcm.tmc.edu/projects...013/vcf_files/

    Comment

    • id0
      Senior Member
      • Sep 2012
      • 130

      #3
      Originally posted by aaronh View Post
      Here are the VCF files from the DGRP: http://www.hgsc.bcm.tmc.edu/projects...013/vcf_files/
      That looks great!

      Which genome version is that? I couldn't find that info on the DGRP website.

      Comment

      • aaronh
        Member
        • Sep 2008
        • 46

        #4
        It is either flybase 5.something or dm3. They are the same thing, just with or without the leading chr.

        Comment

        • id0
          Senior Member
          • Sep 2012
          • 130

          #5
          Originally posted by aaronh View Post
          It is either flybase 5.something or dm3. They are the same thing, just with or without the leading chr.
          I saw that the positions are without the leading "chr", so that did not look like dm3. Thanks for clarifying that the actual coordinates should be identical.

          Comment

          • spvensko
            Junior Member
            • Mar 2013
            • 4

            #6
            I've worked extensively with the DGRP and can find out which reference was used if it's vital information. My understanding, however, is that most of the revisions of the reference have been annotation and not modifications to the sequence (though I've only heard this - never checked myself).

            Comment

            • id0
              Senior Member
              • Sep 2012
              • 130

              #7
              Originally posted by spvensko View Post
              I've worked extensively with the DGRP and can find out which reference was used if it's vital information. My understanding, however, is that most of the revisions of the reference have been annotation and not modifications to the sequence (though I've only heard this - never checked myself).
              I assume the sequence is stable by now as this is a common organism, genome is fairly small and has not been updated in a while. However, I have no experience with the fly genome, so I am not sure if there are any caveats.

              I am trying to do recalibration, so it's fairly important that the positions are accurate.

              Comment

              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, 10-22-2026, 11:13 AM
              0 responses
              26 views
              0 reactions
              Last Post SEQadmin2  
              Started by SEQadmin2, 10-22-2026, 10:48 AM
              0 responses
              20 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
              43 views
              0 reactions
              Last Post SEQadmin2  
              Working...