I'd like to align my trimmed 454 metagenomic reads to a reference sequence and generate plots of the coverage / percent identity / recruitment.
Both the reads file and the reference file are in fasta format. I don't have access to the original .sff files from the 454 sequencer.
I think consed can align reads like this but I cannot get it to work to align 2 fasta files and the documentation is almost no help. If anyone knows how to get consed to do this that would be great.
Otherwise, I am completely open to suggestions of other pieces of software. I am currently aligning the reads to the reference sequence using fr-hit (http://weizhong-lab.ucsd.edu/frhit/) but I don't know how to plot the resulting data into a 'percent identity plot' or 'recruitment plot'. Any help would be greatly appreciated.
Thanks!
I can align it with a reference sequence (blast, fr-hit, etc) but I need something to plot it. I will take a look at R.