Seqanswers Leaderboard Ad

Collapse

Announcement

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

  • Bowtie Error Message

    Hello,

    I am trying to map some human reads with Bowtie, and after running the program, I received the message below and did not obtain statistics for mapping. It did apparently map 77.5 million reads with the options added (I did a line count on the output file), but I am not sure if Bowtie finished mapping the reads. The input fastq file came from SRA. I have the most recent version of Bowtie for Linux. Does anyone have any suggestions on how to avoid this error so that Bowtie finishes mapping the reads?

    $ ./bowtie -a -v 2 -m 3 hg19_c -C -q --suppress 1,6,7,8 invitro_1.fastq >invitro_1_mapped.txt

    Saw ASCII character -1 but expected 33-based Phred qual.
    Command: ./bowtie -a -v 2 -m 3 -C -q --suppress 1,6,7,8 hg19_c invitro_1.fastq

    Thanks,
    Clayton

  • #2
    Bowite has many options for different formats of quality score,the default is --phred33-quals,which means the inputs(quality scores) are taken as ASCII characters.
    However,it seems that your RNA-Seq data were SOLiD color space format,and usually SOLiD platforms output quality scores in integer.
    So,try this option "--integer-quals" instead of the default one,I think that is the problem.

    Comment

    Latest Articles

    Collapse

    • seqadmin
      Essential Discoveries and Tools in Epitranscriptomics
      by seqadmin




      The field of epigenetics has traditionally concentrated more on DNA and how changes like methylation and phosphorylation of histones impact gene expression and regulation. However, our increased understanding of RNA modifications and their importance in cellular processes has led to a rise in epitranscriptomics research. “Epitranscriptomics brings together the concepts of epigenetics and gene expression,” explained Adrien Leger, PhD, Principal Research Scientist...
      04-22-2024, 07:01 AM
    • seqadmin
      Current Approaches to Protein Sequencing
      by seqadmin


      Proteins are often described as the workhorses of the cell, and identifying their sequences is key to understanding their role in biological processes and disease. Currently, the most common technique used to determine protein sequences is mass spectrometry. While still a valuable tool, mass spectrometry faces several limitations and requires a highly experienced scientist familiar with the equipment to operate it. Additionally, other proteomic methods, like affinity assays, are constrained...
      04-04-2024, 04:25 PM

    ad_right_rmr

    Collapse

    News

    Collapse

    Topics Statistics Last Post
    Started by seqadmin, 04-11-2024, 12:08 PM
    0 responses
    59 views
    0 likes
    Last Post seqadmin  
    Started by seqadmin, 04-10-2024, 10:19 PM
    0 responses
    57 views
    0 likes
    Last Post seqadmin  
    Started by seqadmin, 04-10-2024, 09:21 AM
    0 responses
    51 views
    0 likes
    Last Post seqadmin  
    Started by seqadmin, 04-04-2024, 09:00 AM
    0 responses
    56 views
    0 likes
    Last Post seqadmin  
    Working...
    X