Unconfigured Ad

Collapse
X
 
  • Time
  • Show
Clear All
new posts
  • Carmen
    Member
    • Aug 2012
    • 10

    #1

    uniquely mapped reads

    Hi,

    Is there anyway to report ONLY uniquely mapped reads in bowtie sam output?
  • MGineste
    Member
    • Feb 2011
    • 21

    #2
    Salut Carmen,

    The method will depend on the version of bowtie you are using.

    Are you using bowtie1 or bowtie2 ?

    Mathieu

    Comment

    • MGineste
      Member
      • Feb 2011
      • 21

      #3
      My previous reply is inappropriate.

      I posted a way to filter out multiple alignments from a SAM file, there : http://seqanswers.com/forums/showpos...45&postcount=6

      Hope this will solve your problem,
      Mathieu

      Comment

      • Carmen
        Member
        • Aug 2012
        • 10

        #4
        OK Mathieu,
        I will try your way

        Thanks for your replay

        Comment

        • Carmen
          Member
          • Aug 2012
          • 10

          #5
          Dear Mathieu,
          I used the grep command for the XS tag but in the sam output of bowtie-0.12.7 (the version I used) there isn't this tag

          Any other suggestion??

          Carmen

          Comment

          • MGineste
            Member
            • Feb 2011
            • 21

            #6
            Well, it seems that my initial question (version of bowtie) was in the end appropriate.

            In bowtie1, there is an option to report uniquely mapped reads only. From the bowtie1 manual :

            -m <int>

            Suppress all alignments for a particular read or pair if more than <int> reportable alignments exist for it. Reportable alignments are those that would be reported given the -n, -v, -l, -e, -k, -a, --best, and --strata options. Default: no limit. Bowtie is designed to be very fast for small -m but bowtie can become significantly slower for larger values of -m. If you would like to use Bowtie for larger values of -k, consider building an index with a denser suffix-array sample, i.e. specify a smaller -o/--offrate when invoking bowtie-build for the relevant index (see the Performance tuning section for details).
            Using -m 1 should fill your needs.

            Mathieu

            Comment

            • Carmen
              Member
              • Aug 2012
              • 10

              #7
              I have already used the option -m 1
              with this option the uniquely mapped reads are reported as number in the final report but in the final sam output file there are all the reads
              I'm interested in a file in which are reported only the uniquely mapped reads

              Carmen

              Comment

              • MGineste
                Member
                • Feb 2011
                • 21

                #8
                I would then switch to bowtie2 and use the method mentioned above.

                Mathieu

                Comment

                • Carmen
                  Member
                  • Aug 2012
                  • 10

                  #9
                  I will try two strategies
                  alignment with bowtie2
                  extraction of uniquely mapped reads from modified sam file with R

                  Carmen

                  Comment

                  Latest Articles

                  Collapse

                  • SEQadmin2
                    Beyond CRISPR/Cas9: Understand, Choose, and Use the Right Genome Editing Tool
                    by SEQadmin2



                    CRISPR/Cas9 sparked the gene editing revolution for both research and therapeutics.1 But this system still showed severe issues that limited its applications. The most prominent were the heavy reliance on PAM sequences, delivery limitations, double-stranded breaks that prompt unintended edits and cell death, and editing inefficiency (both in targeting and in knock-in reliability).

                    Despite this, “CRISPR helped turn genome editing from a specialized technique into
                    ...
                    07-31-2026, 11:01 AM
                  • SEQadmin2
                    Proteomic Platforms: How to Choose the Right Analytical Strategy to Improve Detection and Clinical Applications
                    by SEQadmin2


                    Proteomics platforms are evolving rapidly, with advances in mass spectrometry and affinity-based approaches expanding what researchers can detect and at what scale. As the field moves toward deeper proteome coverage and clinical applications, scientists face an increasingly complex landscape of tools. This article will explore how researchers are navigating these choices to find the right platform for their work.

                    The systematic characterization of the human proteome has
                    ...
                    07-20-2026, 11:48 AM
                  • SEQadmin2
                    Advanced Sequencing Platforms Tackle Neuroscience’s Toughest Genomics Problems
                    by SEQadmin2



                    Genomics studies in neuroscience face a special challenge due to the brain’s complexity and scarcity of samples. Mapping changes in cell type and state using conventional next-generation sequencing methods remains challenging. Advances in technologies like single-cell sequencing, spatial transcriptomics, and long-read sequencing have opened the door to deeper studies of the brain and diseases like Alzheimer’s, amyotrophic lateral sclerosis (ALS), and schizophrenia.
                    ...
                    07-09-2026, 11:10 AM

                  ad_right_rmr

                  Collapse

                  News

                  Collapse

                  Topics Statistics Last Post
                  Started by SEQadmin2, 07-31-2026, 02:55 AM
                  0 responses
                  19 views
                  0 reactions
                  Last Post SEQadmin2  
                  Started by SEQadmin2, 07-24-2026, 12:17 PM
                  0 responses
                  16 views
                  0 reactions
                  Last Post SEQadmin2  
                  Started by SEQadmin2, 07-23-2026, 11:41 AM
                  0 responses
                  16 views
                  0 reactions
                  Last Post SEQadmin2  
                  Started by SEQadmin2, 07-20-2026, 11:10 AM
                  0 responses
                  26 views
                  0 reactions
                  Last Post SEQadmin2  
                  Working...