Unconfigured Ad

Collapse
X
 
  • Time
  • Show
Clear All
new posts
  • Boel
    Member
    • Oct 2009
    • 62

    #1

    Bowtie poroblem when mapping against short sequences, no positions.

    Hi All,

    I want to use Bowtie to align reads to exons and junctions. I have created fasta files of the junctions and exons, indexed them and so on. When I run bowtie I end up with aligned reads without mapping information.

    Code:
    WICMT-SOLEXA_100421_61T4HAAXX:6:25:11235:11821#0/1;0	4	*	0	0	*	*	0	0	CGGGGCATAGGGGTACTTCTCAAGTGGGGAATGCCATATGAAGTGGAGCATACATGGGGGCACACAATTCCA@#######################################################################	XM:i:0
    WICMT-SOLEXA_100421_61T4HAAXX:6:25:11235:13629#0/1;1	4	*	0	0	*	*	0	0	GTCCCGGCTCACTCAACCTCCACTTCCCAGGTTCAAGCGATTCTCCTGCCTCAGGCTCCCAAGTAGCTGGGAGGGGGGGGGGGGGGGGGGGGGGGGGFGGGGFCGGFGGFGFGDGGGGGGGGFGGECFEEFFEDFCFEEEFDBC	XM:i:0
    WICMT-SOLEXA_100421_61T4HAAXX:6:25:11235:17639#0/1;1	4	*	0	0	*	*	0	0	CCAGACCGTATTCCACCGCTTCAGGGGCGGAAAGGAAGCGATCGCGCTCGGTATCACGTTCAATCTGTTCTAGGGGGGGGGGGGGGGFGGGGGGGGGGGGGGGGGGEGGGGDFGGGGFEFFGGDGFGFFGEFGFFFDFGEGGGG	XM:i:0
    I know that spaces and pipes in the reference names can be a problem, so I don't have those in my names. The reference names are however quite long (chr1:196945439-196945639:+:ENSG00000081237 and similar). Names such as ENSG00000081237_1_196945439_196945639 makes no difference.

    I'm using bowtie version 0.12.7.

    Would truly appreciate some help!
    Boel
    Last edited by Boel; 01-14-2011, 09:15 AM. Reason: typo
  • Boel
    Member
    • Oct 2009
    • 62

    #2
    Problem solved.

    The flag is 4 = unmapped reads.

    Unable to delete my first message - sorry about that.

    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

    ad_right_rmr

    Collapse

    News

    Collapse

    Topics Statistics Last Post
    Started by SEQadmin2, Yesterday, 12:22 PM
    0 responses
    12 views
    0 reactions
    Last Post SEQadmin2  
    Started by SEQadmin2, 08-11-2026, 10:35 AM
    0 responses
    13 views
    0 reactions
    Last Post SEQadmin2  
    Started by SEQadmin2, 08-06-2026, 07:41 AM
    0 responses
    30 views
    0 reactions
    Last Post SEQadmin2  
    Started by SEQadmin2, 08-03-2026, 10:13 AM
    0 responses
    48 views
    0 reactions
    Last Post SEQadmin2  
    Working...