I am pretty new to bioinformatics, and I was hoping that I could get some help with a bowtie2 script that I am putting together.
I am aligning ChIP-seq paired-end reads (2 samples: Input control and ChIP sample) to a reference and I want to include a minimum fragment size of 200bp and maximum fragment size of 600bp. A pseudocode version of my script is below.
/(path)/bowtie2 —I 200 —X 600 -x /(path)/genomeIndex -1 (chip/IN).fastq -2 (chip/IN).fastq -S alignment.sam
When I run this code, I get the error:
"Extra parameter(s) specified: "—I", "200", "—X", "600"
Note that if <mates> files are specified using -1/-2, a <singles> file cannot
also be specified. Please run bowtie separately for mates and singles.
Error: Encountered internal Bowtie 2 exception (#1)"
and:
"(ERR): bowtie2-align exited with value 1"
I am not specifying any singles files, only mate pair files, so I am thoroughly confused. Any suggestions?
I am aligning ChIP-seq paired-end reads (2 samples: Input control and ChIP sample) to a reference and I want to include a minimum fragment size of 200bp and maximum fragment size of 600bp. A pseudocode version of my script is below.
/(path)/bowtie2 —I 200 —X 600 -x /(path)/genomeIndex -1 (chip/IN).fastq -2 (chip/IN).fastq -S alignment.sam
When I run this code, I get the error:
"Extra parameter(s) specified: "—I", "200", "—X", "600"
Note that if <mates> files are specified using -1/-2, a <singles> file cannot
also be specified. Please run bowtie separately for mates and singles.
Error: Encountered internal Bowtie 2 exception (#1)"
and:
"(ERR): bowtie2-align exited with value 1"
I am not specifying any singles files, only mate pair files, so I am thoroughly confused. Any suggestions?
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