Hi all, I am working on a plant 454 genomic data, that has been prepared in one of my colleagues' lab. recently i had chance to get some data from an another lab that has sequenced the same plant with 454 tech. For some reason they are not sharing raw data, but only contigs they have built. So is it wise to merge two results' datum and use contigs as reads, and re-assemble ?Has anyone out there did something close to this? Thank you in advance..V.G.