ADD COMMENT
• link
updated 4.1 years ago by
Juke34
8.6k
•
written 4.1 years ago by
Ric
▴
430
1
Entering edit mode
softmasking (or hard masking) has nothing to do with the way you detect repeats, it's just ho you mask the genome afterwards.
what you mention here is mainly to detect (de-novo) repeats in your genome. Afterwards you will need to get the resulting repeats and use them to mask the genome
1 - Creating a repeat library (what you perform using RepeatModeler (in some steps RepeatMasker can be used to e.g classify the repeat in your library))
2 - Using repeat library/libraries to mask a genome (What you perform using RepeatMasker)
You can use a de-novo repeat library made with RepeatModeler and/or You can use Repbase and/or Dfam
Download the Dfam.hmm.gz library from http://www.dfam.org and save it
to the RepeatMasker/Libraries directory. Uncompress the file before
using RepeatMasker. The RepeatMasker distribution contains the Dfam
2.0 library.
So if yo have installed it using conda it should be save here ${CONDA_PREFIX}/share/RepeatMasker/Libraries
softmasking (or hard masking) has nothing to do with the way you detect repeats, it's just ho you mask the genome afterwards.
what you mention here is mainly to detect (de-novo) repeats in your genome. Afterwards you will need to get the resulting repeats and use them to mask the genome
Aren't those hidden markov models you are linking to?
Yes, I would like to detect (de-novo) repeats in your genome. Therefore, I changed my question above.