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I am working on a workflow for a hybrid denovo assembly of 454 and illumina data using the CLC genomics workbench. I was wondering if anyone has done similar work, and if so what steps they took to get optimal results.
Thanks
Thanks
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Dear BardJ. Sorry about the late answer. I was just splunking through SeqAnswers, and I found your question. Hybrid assemblies are a common use of the Workbench. I can send you a publication that references this work. In general, there are separate assembly criteria for each type of data, and the default criteria are a good place to start. Since you posted, the de novo assembler is even more efficient. I hope you gave it a try. If not, try it again now.
Best,
Naomi
(employee of CLC)
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