Thank you.
I do not have any additional reads to use for scaffolding, all I have is illumina Mi-seq paired end data. I still just tried to use SSPACE with denovo assembled genome file and paired end data(same ones, used for denovo assembly). It resulted in exact same number of contigs observed in the denovo assembled file.
It looks like if I do not have any additional reads, I cannot do anything further to improve the assembly?
Can you please provide some information on the "extra/additional reads" ?