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
We have to assemble a genome with the following features:
Genome size: ~2Gb
High repetitiveness: ~78.68% (inferred from a close species)
Hi AT content: ~72.36% (inferred from a close species)
PacBio HiFi sequencing: 130x coverage
We've checked some of the issues, such as #239 and we thought about the following tests. So, we'd like to ask your opinion or recommendations about them. All of them have two steps: (a) assembly with wtdbg2; (b) polishing with wtdbg-cns (minimap2 is used as a read mapper).
Hello @ruanjue !
We have to assemble a genome with the following features:
We've checked some of the issues, such as #239 and we thought about the following tests. So, we'd like to ask your opinion or recommendations about them. All of them have two steps: (a) assembly with wtdbg2; (b) polishing with wtdbg-cns (minimap2 is used as a read mapper).
List of possible tests/ideas:
wtdbg2 -g 2.05g -t 24 -x sq
wtdbg2 -g 2.05g -t 24 -x ccs
wtdbg2 -g 2.05g -t 24 -x sq -R
Increase -s parameter (0.5 or 0.7 as in Parameters for triploid HIFI #239):
wtdbg2 -g 2.05g -t 24 -x sq -s 0.5
Try to vary -L, increasing it to keep the longest reads.
Any advice would be appreciated,
Thanks in advance
The text was updated successfully, but these errors were encountered: