Seqanswers Leaderboard Ad

Collapse

Announcement

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

  • Bowtie. Different outputs from equivalent(?) inputs.

    Hello all

    I'm currently trying to align & annotate lots of short sequences to the human genome (from Ensembl) using Bowtie (and R).

    When the query sequences are given on the command line (with -c) as a comma-separated list I cannot make get Bowtie to yield the same result when using a self-created FASTQ-file. The suspected error is what I choose as default (Phred) read qualities in the FASTQ-file. It is clear that if Bowtie is given sequences on the command line it must assume some default read qualities, but what is the default value? I cannot find the answer in the Bowtie manual but I suspect, that the answer is Phred quality 40 (corresponding to ASCII character "h"(?)) since this quality is used with other commands.

    Using "h" as default read-quality, however, does not give exactly the same results? Where am I taking the wrong turn?

    Minimal example: Running

    bowtie -a --fullref Homo_sapiens.GRCh37.63.cdna.all TestFASTQ.fq test1.txt
    bowtie -c -a --fullref Homo_sapiens.GRCh37.63.cdna.all AAATTGCTCTTAGCATA test2.txt

    where the TestFASTQ.fq is simply

    @Seq1
    AAATTGCTCTTAGCATA
    +
    hhhhhhhhhhhhhhhhh

    does not give the the same results.

    The output from my R-script is (which filters and formats the bowtie output)

    > genes1
    [1] "ENSG00000135829" "ENSG00000135829" "ENSG00000135829" "ENSG00000151789"
    [5] "ENSG00000127081" "ENSG00000122042" "ENSG00000162894" "ENSG00000187699"
    [9] "ENSG00000187699" "ENSG00000231890" "ENSG00000182749" "ENSG00000233124"
    [13] "ENSG00000228002" "ENSG00000101040" "ENSG00000101040" "ENSG00000112773"
    [17] "ENSG00000112773" "ENSG00000112773"
    > genes2
    [1] "ENSG00000135829" "ENSG00000135829" "ENSG00000135829" "ENSG00000151789"
    [5] "ENSG00000127081" "ENSG00000122042" "ENSG00000162894" "ENSG00000231890"
    [9] "ENSG00000187699" "ENSG00000187699" "ENSG00000182749" "ENSG00000233124"
    [13] "ENSG00000228002" "ENSG00000101040" "ENSG00000101040" "ENSG00000112773"
    [17] "ENSG00000112773" "ENSG00000112773"

    (EDIT: The two vectors above differs at positions 8 and 10)

    Can anyone help me?

    Thanks!
    AEB

    ps. does anyone know, how to make Bowtie return Gene Symbols. I.e. get DHX9 for ENSG00000135829 and so on.
    Last edited by AEB; 08-18-2011, 01:41 AM.

  • #2
    You should use the org.Hs.eg.db bioconductor package to convert between human gene symbol and Ensembl IDs

    Comment

    Latest Articles

    Collapse

    • seqadmin
      Recent Advances in Sequencing Analysis Tools
      by seqadmin


      The sequencing world is rapidly changing due to declining costs, enhanced accuracies, and the advent of newer, cutting-edge instruments. Equally important to these developments are improvements in sequencing analysis, a process that converts vast amounts of raw data into a comprehensible and meaningful form. This complex task requires expertise and the right analysis tools. In this article, we highlight the progress and innovation in sequencing analysis by reviewing several of the...
      05-06-2024, 07:48 AM
    • 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

    ad_right_rmr

    Collapse

    News

    Collapse

    Topics Statistics Last Post
    Started by seqadmin, Yesterday, 06:57 AM
    0 responses
    12 views
    0 likes
    Last Post seqadmin  
    Started by seqadmin, 05-06-2024, 07:17 AM
    0 responses
    16 views
    0 likes
    Last Post seqadmin  
    Started by seqadmin, 05-02-2024, 08:06 AM
    0 responses
    19 views
    0 likes
    Last Post seqadmin  
    Started by seqadmin, 04-30-2024, 12:17 PM
    0 responses
    24 views
    0 likes
    Last Post seqadmin  
    Working...
    X