Hi,
downloading ftp://ftp.ebi.ac.uk/pub/databases/Rfam/CURRENT/Rfam.tar.gz file.
Create one Rfam.fasta file from above link.
makeblastdb using Rfam.fasta
blastn srna_reads.fa using Rfam.fasta as Database.
filter reads corresponds to rRNA, tRNA, snRNA, snoRNA.
Is this a correct way of doing filtering rRNA, tRNA, snRNA, snoRNA reads?
Thanks,
Manoharan