Unconfigured Ad

Collapse
X
 
  • Time
  • Show
Clear All
new posts
  • wmseq
    Member
    • May 2011
    • 71

    #1

    Do I need to create an index for my reference genome?

    Hi every one,
    After I aligned the reads of my samples with tophat, do I need to to create an index for my reference genome like after bowtie2 alignment, and then convert/sort/index all my sam files to identify the upregulated and down-regulated genes from a compound treatment?
    Thanks a lot!!
    Richard
  • dpryan
    Devon Ryan
    • Jul 2011
    • 3478

    #2
    No, you don't need to do that.

    Comment

    • wmseq
      Member
      • May 2011
      • 71

      #3
      Thank you, dpryan!!
      Do I need to convert/sort/index all my sam files, because I saw a question on a problem with unsorted bam files for HTSeq-count?

      Comment

      • dariober
        Senior Member
        • May 2010
        • 311

        #4
        Originally posted by wmseq View Post
        Thank you, dpryan!!
        Do I need to convert/sort/index all my sam files, because I saw a question on a problem with unsorted bam files for HTSeq-count?
        From my memory I recall tophat produces bam files sorted by position. htseq-count needs sam files sorted by read name only if the reads are paired-end. If they are single end I don't think the order matters.

        Comment

        • wmseq
          Member
          • May 2011
          • 71

          #5
          But I read a tutorial, it seams that all sam files should be convert/sort/indexed. I am not sure.

          Comment

          • dpryan
            Devon Ryan
            • Jul 2011
            • 3478

            #6
            If you have paired end reads, then you need to name sort the file (usually you would sort a BAM file, rather than a SAM file). There's no need to create an index when using htseq-count, it will ignore it.

            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, 10-15-2026, 10:52 AM
            0 responses
            28 views
            0 reactions
            Last Post SEQadmin2  
            Started by SEQadmin2, 10-14-2026, 05:39 AM
            0 responses
            36 views
            0 reactions
            Last Post SEQadmin2  
            Started by SEQadmin2, 10-13-2026, 09:56 AM
            0 responses
            31 views
            0 reactions
            Last Post SEQadmin2  
            Started by SEQadmin2, 10-09-2026, 11:14 AM
            0 responses
            29 views
            0 reactions
            Last Post SEQadmin2  
            Working...