Entering edit mode
10.5 years ago
ab.tsubaki
▴
50
Hi there
In need of help please!
I'm masking the repetitive regions in my wheat sequencing data using RepeatMasker. This generates a .masked file. Next I want to map or compare this masked file to other genome sequences but BWA uses fastq if I remember correctly. How can I convert the .masked file to a useable format? Or can it be used as-is???
Appreciate any comments, suggestions or previous experience :-)
Anandi
Do you have to use BWA? It's intended for short reads, not whole genome comparisons. Why don't you just use a tool designed to compare genomes?
Well, I'm not QUITE comparing a whole genome. My contigs are quite short and that's what I'll be mapping first.
Any advice on other mapping programs will be appreciated? I know BWA and Bowtie and I don't think either of them makes mention of .masked files?
The .masked file is just a fasta file, at least that's my recollection.
Thanks! I looked at the output from RepeatMasker and saw that it's a fasta file just now! Clever me!