Announcement

Collapse
No announcement yet.
X
 
  • Filter
  • Time
  • Show
Clear All
new posts

  • bowtie output

    Hi, I am a newbie in bioinformatics. I am trying to use bowtie to map a set of sequences. Here is the result I have got.

    Time loading forward index: 00:00:12
    Time loading mirror index: 00:00:13
    Seeded quality full-index search: 07:49:33
    # reads processed: 440372
    # reads with at least one reported alignment: 193962 (44.05%)
    # reads that failed to align: 246410 (55.95%)
    Reported 1903683060 alignments to 1 output stream(s)
    Time searching: 07:49:58
    Overall time: 07:49:59

    Is there a way to display more information than it is above? For example, the percentage of reads that are uniquely mapped. Thanks.

  • #2
    Hi, I'm also new, but I think I can help you out.

    In the command line when you told bowtie to align your query sequence file(s) did you specify a directory for the output or did you just name it?

    If you specified a directory you'll find the txt file in that directory and you can open it up and view it using your favorite text editor. If you have problems viewing it you can upload the file to Galaxy (http://main.g2.bx.psu.edu/) and view it there. I know sometimes I'll try to open the bowtie outputs in Windows and they won't open.

    Example: bowtie <options> index query /../.../..../..../file.map

    If you didn't specify a directory for the bowtie output then you will find it in your bowtie folder.

    Example: bowtie <options> index query file.map


    Hope this helps.

    -Brandon

    Comment


    • #3
      Thanks for your reply. I am not sure about the map file. Is that the mapping output?

      Here is the command I have used.

      bowtie mm9 -r -n 1 -l 36 -a sequences-input -t > mapping

      The mapping result is stored in the mapping.


      But these info are displayed on the terminal.

      Time loading forward index: 00:00:12
      Time loading mirror index: 00:00:13
      Seeded quality full-index search: 07:49:33
      # reads processed: 440372
      # reads with at least one reported alignment: 193962 (44.05%)
      # reads that failed to align: 246410 (55.95%)
      Reported 1903683060 alignments to 1 output stream(s)
      Time searching: 07:49:58
      Overall time: 07:49:59

      Comment


      • #4
        I'm not sure if there is a way to produce a file with an outline of different aspects of your alignment, but to address your unique reads mapped question you could try the following parameters:

        Use "-k 1" (which is a Bowtie default) instead of "-a"
        This will cause Bowtie to report the first valid alignment it encounters. I'm going to assume all others that align to the same position will not be added to the alignment file and thus you'd be able to view the percentage and number of "reads with at least one reported alignment" using the -t option.

        In theory I think the above solution will work for the query you had. I would definitely consult the Bowtie manual, it is a wealth of information.

        -Brandon

        Comment


        • #5
          Well, I think the command would be as follows:
          bowtie mm9 -r -n 1 -l 36 -a sequences-input -t 2> result

          Maybe you should replace > with 2>

          Comment

          Latest Articles

          Collapse

          • seqadmin
            Advanced Tools Transforming the Field of Cytogenomics
            by seqadmin


            At the intersection of cytogenetics and genomics lies the exciting field of cytogenomics. It focuses on studying chromosomes at a molecular scale, involving techniques that analyze either the whole genome or particular DNA sequences to examine variations in structure and behavior at the chromosomal or subchromosomal level. By integrating cytogenetic techniques with genomic analysis, researchers can effectively investigate chromosomal abnormalities related to diseases, particularly...
            09-26-2023, 06:26 AM
          • seqadmin
            How RNA-Seq is Transforming Cancer Studies
            by seqadmin



            Cancer research has been transformed through numerous molecular techniques, with RNA sequencing (RNA-seq) playing a crucial role in understanding the complexity of the disease. Maša Ivin, Ph.D., Scientific Writer at Lexogen, and Yvonne Goepel Ph.D., Product Manager at Lexogen, remarked that “The high-throughput nature of RNA-seq allows for rapid profiling and deep exploration of the transcriptome.” They emphasized its indispensable role in cancer research, aiding in biomarker...
            09-07-2023, 11:15 PM
          • seqadmin
            Methods for Investigating the Transcriptome
            by seqadmin




            Ribonucleic acid (RNA) represents a range of diverse molecules that play a crucial role in many cellular processes. From serving as a protein template to regulating genes, the complex processes involving RNA make it a focal point of study for many scientists. This article will spotlight various methods scientists have developed to investigate different RNA subtypes and the broader transcriptome.

            Whole Transcriptome RNA-seq
            Whole transcriptome sequencing...
            08-31-2023, 11:07 AM

          ad_right_rmr

          Collapse

          News

          Collapse

          Topics Statistics Last Post
          Started by seqadmin, Yesterday, 06:57 AM
          0 responses
          9 views
          0 likes
          Last Post seqadmin  
          Started by seqadmin, 09-26-2023, 07:53 AM
          0 responses
          8 views
          0 likes
          Last Post seqadmin  
          Started by seqadmin, 09-25-2023, 07:42 AM
          0 responses
          14 views
          0 likes
          Last Post seqadmin  
          Started by seqadmin, 09-22-2023, 09:05 AM
          0 responses
          44 views
          0 likes
          Last Post seqadmin  
          Working...
          X