Unconfigured Ad

Collapse
X
 
  • Time
  • Show
Clear All
new posts
  • Ilarius
    Junior Member
    • Nov 2016
    • 2

    #1

    mapping 35bp solid reads with tophat unsuccessful

    Hi, I recently downloaded some solid short reads (35 bp), single end, and convert them in cfasta with ahi-dump.

    I found that there are very few mappers that support solid read mapping in color space and finally i decided to use tophat using bowtie1 (which supported color space mapping).
    Unfortunately I less less than 30 % of the reads mapping.
    My previous experience has always been with 100 bp paired end reads, so I am not completely sure if I am using the right parameters for short read mapping:

    tophat -G $annotation --segment-length 17 --segment-mismatches 1 -g 1 --bowtie1 -p 12 -o $OUTPUT_FOLDER --coverage-search --color --quals $genome $READ $QUAL

    maybe is the segment-mismatch and maximum multi-hits too restrictive? (-g is 20 by default). What for your experience are the best parameters for short read mapping?

    Thanks
    Ilario
  • colindaven
    Senior Member
    • Oct 2008
    • 417

    #2
    In general, in comparison to Illumina PE reads don't expect high mapping percentages. From memory I think 50-70% was pretty good, as the data were not extensively filtered (on the 5500xl machine at least).

    You probably don't want to use Tophat for such short reads as I don't think it will be able to find anchors/seeds successfully.

    My best experiences with SOLiD were with the commercial program NovoalignCS. You might be able to get a free trial.

    Otherwise, Shrimp2 was also not too bad.

    Why not use just bowtie1 instead of tophat2 with bowtie1 ?

    Comment

    • Ilarius
      Junior Member
      • Nov 2016
      • 2

      #3
      I did use tophat2 with bowtie1, anyway if I let the default -g option (i think it is 20) it takes ages to finish.

      As regards shrimp I didn't find any working link to download it!

      Comment

      • colindaven
        Senior Member
        • Oct 2008
        • 417

        #4
        I recently found another non-commercial aligner for SOLiD data - it is called subread. I have only tried for Illumina data but it's very good there.

        Again, I wouldn't use tophat for such short read data.

        Comment

        • gringer
          David Eccles (gringer)
          • May 2011
          • 845

          #5
          What for your experience are the best parameters for short read mapping?
          Anything that gets you quicker to re-analysing your target sample with a non-SOLiD system. You shouldn't be mapping SOLiD reads at all, especially not 35bp ones; interpreting the results is just too confusing (even for the people writing code to do the mapping).

          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, Today, 11:13 AM
          0 responses
          10 views
          0 reactions
          Last Post SEQadmin2  
          Started by SEQadmin2, Today, 10:48 AM
          0 responses
          10 views
          0 reactions
          Last Post SEQadmin2  
          Started by SEQadmin2, 10-15-2026, 10:52 AM
          0 responses
          32 views
          0 reactions
          Last Post SEQadmin2  
          Started by SEQadmin2, 10-14-2026, 05:39 AM
          0 responses
          40 views
          0 reactions
          Last Post SEQadmin2  
          Working...