Hi Katy the SourceForge page is dead since years. Please repost your support request on GitHub: https://github.com/simon-anders/htseq/issues Simon
htseq count problem
last commit to Sourceforge SVN; new repo is htt...
htseq-count: option to count all alignments.
BAM and SAM readers cannot parse "=" in CIGAR format
Htseq throws error for exonic read counts
Implemented new functions in BAM_Reader and BAM...
Modified version checking behaviour to work pro...
HTSeq count txt file first line empty
updates to documentation
status: open --> closed
No, because htseq-count is specifically designed for differential-expression calling,...
Paired end reads, bacterial genome
tagging 0.6.1p1
fixed wrong version number in _version.py
tagging release 0.6.1
Counts on single and paired ends reads merged bam file
one more question added to htseq-count FAQ
minor formatting in docs
version 0.6.1
- added BED parser
added otherparsers.rst, which was missing in pr...
moved VCF docu to otherparsers.rst
added GenomicArrayOfSets.svg, which was missing...
version 0.6.0
finished improved htseq-count and updated docum...
count2 now works and is tested
Fixed wiggle parser and some weird syntax error...
WIG_Reader initial draft
fized some more nonsense pair_SAM_alignments_wi...
added 'pair_SAM_alignments_with_buffer', not ye...
Dear Simon, If I interpret you correctly, than this is not a problem that HTSeq would...
If you have aligned to a transcriptome, the each gene is a different reference sequence,...
Sorry, I can't follow your question. It sounds as if you are following some instructions...
UMI Support in htseq-count ( Patch included)
making the count matrix from a fasta reference
htseq counting problem