Mercurial > repos > padge > gtf_to_bed_script
diff README.rst @ 0:ed0d0eda36a9 draft default tip
"planemo upload for repository https://github.com/usegalaxy-be/galaxytools/tree/main/gtf_to_bed commit 66fba7c9dccfddadce13aad591f441c66c3c309b-dirty"
author | padge |
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date | Wed, 29 Sep 2021 13:50:53 +0000 |
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--- /dev/null Thu Jan 01 00:00:00 1970 +0000 +++ b/README.rst Wed Sep 29 13:50:53 2021 +0000 @@ -0,0 +1,19 @@ +bwakit +======= + +Written by Guy Bottu for the GenePattern server of VIB BioinforlmaticsCore, +takes as input a GTF file and writes a BED file in 12 column format +with information about transcripts, for use with RSeqC. + +The "thick" information is about the coding region, ideally it goes from +start codon to stop codon, but is information is lacking (e.g. because +of missing sequence or missing annotation), we use the CDS information. +For some transcripts there are multiple start or stop codons. We amways +choose the "thick" so that is has maximum length. + +If there is no CDS information (as for ncRNA) the "thick" will have just a +repeat of the transcript start position, as per BED convention. + +modified for integration under GenePattern + +usage : perl gtf_to_bed.pl <GTF file> <output file>