I know repeats can be scan through FIMO, for their location in whole genome. But FIMO required MEME-motif file as an input, which mainly contain "letter-probability matrix".
I have read the MEME motif format (http://meme-suite.org/doc/meme-format.html) in detail. I have problem in understanding the concept behind generating the "letter-probability matrix" in MEME-motif format. I am unable to find any software/script which directly converts fasta format to MEME-motif.
So, I have two questions regarding this:
- How to convert single fasta file into this MEME-motif file?
- In case I have multiple copy of fasta file of tandem repeats which are varying at few nucleotide positions only, how to convert these fasta files into one MEME-motif file?