Unconfigured Ad

Collapse
X
 
  • Time
  • Show
Clear All
new posts
  • fcr
    Member
    • Jan 2012
    • 19

    #1

    Programs to filter out the Mitochonrial DNA from Hightroughput Sequencing Reads

    Hi all,

    I have Whole Genome Shotgun Reads (Illumina) of a mammalian species. I am interested in filtering out all the reads matching mitochondrial DNA before starting the downstream analysis. I know the right thing is to blast them or map them against mtDNA. But, Do anyone knows about available software or scripts to do this? I would like to know if there are tools for it before writing the code myself.

    Cheers,
    Fernando
  • peromhc
    Senior Member
    • Sep 2009
    • 108

    #2
    Although I have not tried this very approach, I bet you can use Bowtie combined with the --un feature.. Make a fasta file that contains your mt genome, build the bowtie index, and run.

    Comment

    • swbarnes2
      Senior Member
      • May 2008
      • 910

      #3
      Align to the whole genome, including mtDNA, using bowtie or bwa or whatever. Then you can filter your .bam for reads that align to the mtDNA.

      Comment

      • husamia
        Member
        • Apr 2010
        • 66

        #4
        Originally posted by swbarnes2 View Post
        Align to the whole genome, including mtDNA, using bowtie or bwa or whatever. Then you can filter your .bam for reads that align to the mtDNA.
        I agree. there is no way to know which reads at mt so you have to align first.

        Comment

        • mjp
          Member
          • Mar 2011
          • 25

          #5
          You could build indices with your mapping program of choice and map your reads to it.

          Take a look at http://www.ncbi.nlm.nih.gov/genomes/...2759&hopt=html (Organelle Genome Resources) to download sequences for your indices.

          Hope it helps.

          Comment

          • SES
            Senior Member
            • Mar 2010
            • 275

            #6
            Originally posted by fcr View Post
            Hi all,

            I have Whole Genome Shotgun Reads (Illumina) of a mammalian species. I am interested in filtering out all the reads matching mitochondrial DNA before starting the downstream analysis. I know the right thing is to blast them or map them against mtDNA. But, Do anyone knows about available software or scripts to do this? I would like to know if there are tools for it before writing the code myself.

            Cheers,
            Fernando
            As a sanity check, be sure to BLAST the mtDNA against the genome after you have mapped or assembled your reads. The bowtie --un method is very fast for filtering reads, but unfortunately it does not work in my experience. Sure, it will filter out some reads but when you BLAST your assembly against the organelle genome after assembly it is quite clear that this type of filtering is not really effective.

            It is slower, but I use BLAST for filtering, which leaves no contamination in the final assembly. Either way you choose to go, just keep in mind that checking that the filtering actually worked is quick and easy, and will reduce headaches downstream.

            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
            38 views
            0 reactions
            Last Post SEQadmin2  
            Started by SEQadmin2, 10-22-2026, 10:48 AM
            0 responses
            28 views
            0 reactions
            Last Post SEQadmin2  
            Started by SEQadmin2, 10-15-2026, 10:52 AM
            0 responses
            41 views
            0 reactions
            Last Post SEQadmin2  
            Started by SEQadmin2, 10-14-2026, 05:39 AM
            0 responses
            45 views
            0 reactions
            Last Post SEQadmin2  
            Working...