Hi all!
I used samtools to create sam files from bam. Then I sorted sam file with command: sort -s -k 1,1 07pos.sam > 07pos.sorted.sam...
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Problem with HTSeq dexseq_count.py script
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Cufflinks GTF for DEXSeq
I'm trying to use a Cufflinks GTF that includes novel isoforms as an input for DEXSeq. I'm having trouble with the first python script, which I successfully...
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HTSeq dealing with "*" qualities
Hi everyone,
I started using HTSeq a couple of days ago and now encountered a problem. Maybe someone knows a workaround.
I am...Last edited by kamsen; 04-04-2012, 07:06 AM.
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htseq count missing last mapped fragment
I am using the program htseq-count v0.5.3 with an standard sam file from the mapping of a set of paired end reads. Comparing this file with the output...
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Basic programming question: Very large hash tables
Hi all,
in various applications of RNA-seq analysis I find myself wanting to traverse over all reads in a large fastq file and gather...
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An error in installation of HTSeq with numpy
Hi,
I am trying to install HTSeq and i already checked out if numpy is installed well. but still got an error message that i need...
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Problem using HTSeq
Hi,
I am currently using HTSeq to get raw counts. HTSeq has been installed on our linux cluster and the administrators suggested to use...