Entering edit mode
7.5 years ago
vmicrobio
▴
290
Hi all,
I'm looking for ways and softwares to represent population diversity from fastq (for exemple x% E. coli, y% human, z% P. aeruginosa reads,...)
I intend to do a local blast on different databases then used GRAMMy
Do you guys have some recommendations, comments about this approach? Is it better to start with a with de novo approach before blast? How should I deal with my reads before blast?
Thanks!
What type of data are your fastq?
fastq were obtained by DNA sequencing of biological sample using Proton