You signed in with another tab or window. Reload to refresh your session.You signed out in another tab or window. Reload to refresh your session.You switched accounts on another tab or window. Reload to refresh your session.Dismiss alert
I used braker3 to predict genes in a tree genome (genome size ~900Mb).
The input data:
RNA-seq: RNA extracted from the leaves of the targeted species.
Protein database: orthoDB11- Viridiplantae
Based on the result, the number of genes in the braker.gtf from braker3 is quite low (30313) than augustus.hints.gtf (54829).
The gene number in the closed-related species is about 40000 genes. I guess it's due to the small set of RNA-seq data which did not contained samples from the roots, flowers, and seeds.
Thus, how can I re-run the TSEBRA with the lower weighting of RNA-seq evidence?
The script I used is below: tsebra.py -g ./augustus.hints.gtf -e hintsfile.gff,genemark.gtf -c braker3_adjust.cfg -o ./tsebra_output.gtf
The value of E in the braker3_adjust.cfg is changed from 20 (default) to 1
Is this correct?
Thank you for the help.
The text was updated successfully, but these errors were encountered:
Dear developers,
I used braker3 to predict genes in a tree genome (genome size ~900Mb).
The input data:
Based on the result, the number of genes in the braker.gtf from braker3 is quite low (30313) than augustus.hints.gtf (54829).
The gene number in the closed-related species is about 40000 genes. I guess it's due to the small set of RNA-seq data which did not contained samples from the roots, flowers, and seeds.
Thus, how can I re-run the TSEBRA with the lower weighting of RNA-seq evidence?
The script I used is below:
tsebra.py -g ./augustus.hints.gtf -e hintsfile.gff,genemark.gtf -c braker3_adjust.cfg -o ./tsebra_output.gtf
The value of E in the braker3_adjust.cfg is changed from 20 (default) to 1
Is this correct?
Thank you for the help.
The text was updated successfully, but these errors were encountered: