[maker-devel] Advice on my pipeline
Patrick Tran Van
Patrick.TranVan at unil.ch
Fri Jun 2 03:56:30 MDT 2017
Hello,
This is my first time running Maker for an insect genome annotation.
I have found various resources and tried to make a consensus, I am looking for your thoughts and advices about my pipeline, if I can improve something or doing useless things:
What I have:
- RNA evidence: transcriptome
- Proteine evidence: swissprot/uniprot + busco protein set of insect
- Cegma and busco results of my genome
1) Train SNAP with CEGMA
2) Run (run A) maker with repeat masking with transcript, protein, the new SNAP file (from step 1) and augustus file (from busco).
3) Create SNAP model from run A.
4) Run (run B ) with the new SNAP (done at step 3) with options turned off (est2genome=0) and (protein2genome=0) data, provide gff file (maker_gff=run_A.gff), turn off repeat masking (rm_pass=1), and use previous mapping results (altest_pass=1 and protein_pass=1).
5) Create SNAP model from run B.
6) Run (run C) with the new SNAP (done at step 5) with options turned off (est2genome=0) and (protein2genome=0) data, provide gff file (maker_gff=run_B.gff), turn off repeat masking (rm_pass=1), and use previous mapping results (altest_pass=1 and protein_pass=1).
7) Create SNAP model from run C AND Create Augustus gene model from run C
8) Run (run D) with the new SNAP (done at step 7) + AUGUSTUS file (step 7) with options turned off (est2genome=0) and (protein2genome=0) data, provide gff file (maker_gff=run_C.gff), turn off repeat masking (rm_pass=1), and use previous mapping results (altest_pass=1 and protein_pass=1). + Use keep_preds=1
Does it seems coherent ?
Cheers,
Patrick Tran Van
Groups Chapuisat, Robinson-Rechavi & Schwander
Department of Ecology and Evolution
University of Lausanne
Le Biophore
CH-1015 Lausanne
Switzerland
Office 3206
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