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8.1 years ago
alhicks32188
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0
Hi, I'm a first time user of SPAdes and QUAST, and when I check the quality of my assembled contigs with QUAST, I seem to be getting excessive relocation misassemblies. Does anyone have any insights into possible reasons for this?
Can you provide some additional information about what sort of sequencing this is (technology/cycles)? How many reads did you have? What are the stats from SPAdes/QUAST.
I apologize - this was Illumina Hiseq (I unfortunately don't have any information about the sequencing conditions). For this example sample, there were 4188562 paired end reads. Below is the report from QUAST (note that the local misassemblies are short relocations). Please let me know if I can provide further information or if you have any suggestions.
*All statistics are based on contigs of size >= 500 bp, unless otherwise noted (e.g., "# contigs (>= 0 bp)" and "Total length (>= 0 bp)" include all contigs).