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  • BioSlayer
    Member
    • Feb 2010
    • 26

    bowtie error: extra parameters specified

    I am using bowtie to align short reads against a reference genome (hg19), I prepared the index of the chromosome in the ref genome and exported its location to a bin directory within bowtie as in
    Code:
    export HG_INDEX=/path_to_bowtie/bin/hg
    so as to use it as
    Code:
     $HG_INDEX
    . Then I have the paired end short reads (about 50 bps) that I want to align and save in a sam format, so my command for running that is as follow
    Code:
    bowtie $HG_INDEX -q Combined.fastq -S  aligned.sam
    and it generates an error as (Extra parameter(s) specified: "Combined.fastq", "aligned.sam")
    So changing the command to :
    Code:
    bowtie $HG_INDEX -q Combined.fastq -S  --al aligned.sam
    reduced the complaint to (Extra parameter(s) specified: "Combined.fastq")

    I don't see any options in the bowtie switches that could enable me to avoid this error and searching around different websites looking for solution has proved futile and hence thought the SEQanswers is the best place to share this in hopes of finding a solution..


    Thanks a lot
  • rahilsethi
    Member
    • May 2010
    • 22

    #2
    Extra parameter(s) specified error

    I too have been getting the same error
    I am running bowtie version 0.12.7 for mapping SOLiD (colorspace 50bp read length) data
    against human genome (hg19), on a linux platform (CentOS). When I run with the
    following parameters:

    $bowtie -C -f -Q sample_QV.qual -a --best --strata -n -l 20 --maxbts --chunkmbs 1000 -t --al 50_mapped_reads.csfasta --sam -p 5 /bowtie-ref-build/hg19/hg19 sample.csfasta 50_mapping.sam
    it gives me the following error

    Extra parameter(s) specified: "sample.csfasta", "50_mapping.sam"

    and when I was running with default seed-length(-l) value by not defining
    -l 20 i.e.:

    $bowtie -C -f -Q sample_QV.qual -a --best --strata -n --maxbts --chunkmbs 1000 -t --al 50_mapped_reads.csfasta --sam -p 5 /bowtie-ref-build/hg19/hg19 sample.csfasta 50_mapping.sam
    it runs successfully, generating the number of reads mapped and unmapped
    details on the screen.

    How can I then run the program at different seed length when I run bowtie
    since, as seen above, it does not run whenever I mention seed length
    within permissible range (i.e. 20 > 5 for read length 50bp)?
    Last edited by rahilsethi; 10-07-2011, 10:47 AM.

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