Hi all,
I am working on a project to do a full de novo assembly of a plant
genome. I was interested in SOAPdenovo because it is optimized for
short reads and for large genomes. However, not all of our sequencing
data is Illumina. We have a heterogenous data set that consists of 4
libraries. 1 library is Illumina WGS, 1 is 454 WGS, and then we have
2 paired-end libraries done on 454 (3kb and 20 kb respectively).
Would it be appropriate to try to assemble this data set using
SOAPdenovo?
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