This is part of a series of workflows to annotate a genome, tagged with TSI-annotation
.
These workflows are based on command-line code by Luke Silver, converted into Galaxy Australia workflows.
The workflows can be run in this order:
- Repeat masking
- RNAseq QC and read trimming
- Find transcripts
- Combine transcripts
- Extract transcripts
- Convert formats
- Fgenesh annotation
Steps
ID | Name | Description |
---|---|---|
0 | FGENESH split | fgenesh_split |
1 | FGENESH split | fgenesh_split |
2 | FGENESH annotate | fgenesh_annotate |
3 | FGENESH merge | fgenesh_merge |
4 | FGENESH merge | fgenesh_merge |
5 | FGENESH get mRNA or GC | fgenesh_get_mrnas_gc |
6 | FGENESH get mRNA or GC | fgenesh_get_mrnas_gc |
7 | FGENESH get protein | fgenesh_get_proteins |
8 | Busco | toolshed.g2.bx.psu.edu/repos/iuc/busco/busco/5.5.0+galaxy0 |
Version History
Version 3 (latest) Created 17th Nov 2024 at 23:41 by Anna Syme
Changes made 13 Nov 2024: Added correct input files and connected them to the split steps. Added inputs for db selections in the annotation step. Added lineage input to Busco. Added genome annotation stats derived from gff3 output. Connected in assembly.fasta sequences to "get mRNA/cDNA" tools. Expanded this information text and clarified the need for .cdna .pro and .dat files as input.
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Version 2.1 Created 18th Jun 2024 at 10:08 by Anna Syme
add updated workflow image
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Version-2.1
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Version 1 (earliest) Created 8th May 2024 at 08:28 by Anna Syme
Initial commit
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Created: 8th May 2024 at 08:28
Last updated: 17th Nov 2024 at 23:51
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