Description
The script takes a GENSCAN file as input, and will translate it in gff
format. The GENSCAN format is described here.
Known problem
You must have submited only DNA sequence, without any header!! Indeed the tool expects only DNA
sequences and does not crash/warn if an header is submited along the
sequence. e.g If you have an header ">seq" s-e-q are seen as the 3 first
nucleotides of the sequence. Then all prediction location are shifted
accordingly. (checked only on the online version.
I don't know if there is the same problem elsewhere.)
Type
bash_script
License
GPL-3.0
Keywords
Contributors
Run the following command to execute this component with Nextflow:
cat > params.yaml <<'EOM'
output: "$id.$key.output.gff"
id: "run"
publish_dir: "output/"
EOM
nextflow run https://packages.viash-hub.com/vsh/biobox.git \
-revision v0.4.2 \
-main-script target/nextflow/agat/agat_convert_genscan2gff/main.nf \
-params-file params.yaml Name | Type & Properties |
|---|---|
--genscan -g | file required |
Name | Type & Properties |
|---|---|
--output -o --out --outfile --gff | file required output |
Name | Type & Properties |
|---|---|
--source | string |
--primary_tag | string |
--inflate_type | string |
--verbose | boolean_true |
--config -c | file |