To assemble fastq raw seq read from Ion Torrent for bac genome (3Mb), what are the 'best' commands to get the optimum contig alignment on average (velveth and velvetg).
To assemble fastq raw seq read from Ion Torrent for bac genome (3Mb), what are the 'best' commands to get the optimum contig alignment on average (velveth and velvetg).
Newbler seems to work the best for me so far, for Ion Torrent. VelvetOptimiser worked OK. On a recent de novo assembly with Newbler I got 465 contigs, N50: 17kb, and an assembly size of 4.1 Mb. With VelvetOptimiser, I got 1480 contigs, 3.9 Mb, and N50: 4kb. When I merged with the combiner in CG-Pipeline (which uses Minimus2), I got a final assembly of 454 contigs, N50: 19.5 k, and a genome length of 4.2 Mb.
I have not tried Mira for Ion Torrent and so I cannot comment on that.
i don't think velvet would be good for "homopolymer-ish" data. it is bad for 454 and it behaves even worse for ion torrent.
http://pathogenomics.bham.ac.uk/blog/2011/05/first-look-at-ion-torrent-data-de-novo-assembly/
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this might be a helpful link to get you started: http://dna.med.monash.edu.au/~torsten/velvet_advisor/