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TAMA GO: Degradation Signature
This tool in TAMA-GO is used to assess degradation signature of cDNA libraries and get useful stats about the annotation.
tama_degradation_signature.py
To run tama_degradation_signature.py you first need to run TAMA Collapse with both the "Capped" and "No Cap" algorithms. Both runs should otherwise have identical parameters. The inputs for this tool are the trans_read.bed files from these runs.
USAGE:
python tama_degradation_signature.py -c capped_trans_read.bed -nc nocap_trans_read.bed -o outfile_name
Input explanation:
capped_trans_read.bed - This is the trans_read.bed file that was output from the TAMA Collapse capped run.
nocap_trans_read.bed - This is the trans_read.bed file that was output from the TAMA Collapse no_cap run.
outfile_name - This is the name of the output file which will contain a summary of stats including the degradation signature.
The output will look like this:
Degradation Signature = 0.41700034321 Capped multi-exon, multi-read, transcript count = 61187 No-cap multi-exon, multi-read, transcript count = 35672 Capped total transcript count = 76518 No-cap total transcript count = 49544 Capped single exon trans count = 28755 No-cap single exon trans count = 15854 Capped multi exon trans count = 47763 No-cap multi exon trans count = 33690 Capped total gene count = 21722 No-cap total gene count = 21722 Capped single exon gene count = 11158 No-cap single exon gene count = 11158 Capped multi exon gene count = 10564 No-cap multi exon gene count = 10564 Capped single exon single read gene count = 9794 No-cap single exon single read gene count = 9794 Capped multi exon single read gene count = 2019 No-cap multi exon single read gene count = 2019
Note that gene counts should be the same for the capped and no_cap runs. These numbers are shown for trouble shooting in case the wrong input files are used.
A degradation signature higher than 0.25 is considered high and indicates a large number of degraded products in the sequenced RNA.