Entering edit mode
7.9 years ago
mirza
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180
Hi, I am new to NGS/ genome assembly field. I am given data and assembly (done by someone else) to evaluate if it is correct and if not, do the assembly myself. To check the given draft assembly, I mapped the largest scaffold of the existing reference genome (about 4Mb), using it as query to our draft assembly with blast+ and found that the query scaffold maps to 195 different scaffolds of the draft assembly. 1. I think this means that the assembly is highly fragmented?
The person is justifying this by saying that it is due to the presence of several gaps (Ns) in the query scaffold. Can someone please shed some light on this matter?
Not answering your question, but instead recommending QUAST for assembly quality evaluation.
Thanks but I know about Quast and have all the intentions to use it but this is something very basic which generally doesn't come to mind. So, I want to clarify and what better platform than Biostar.
Please use
ADD REPLY/ADD COMMENTto respond to existing posts to keep threads logically organized.I apologize. I realized after sending it.
No need to apologize. Just wanted to make you aware in case you did not know.