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Hi Søren, many thanks for making such a wonderful tool.
In my current analysis, I have a metagenomic sample which has been sequenced for both short and long reads, but the volume of short reads (~85 Gb) greatly outweighs that of the long reads (4 Gb). As hybrid assembly hasn't been very successful so far, is it possible for Nanomotif to use an assembly generated with short reads as input?
The text was updated successfully, but these errors were encountered:
It is entirely possible. The main concern i the degree of assembly fragmentation, as increased fragmentation leads to fewer motif observations and hence makes motif identification less sensitive.
Hi Søren, many thanks for making such a wonderful tool.
In my current analysis, I have a metagenomic sample which has been sequenced for both short and long reads, but the volume of short reads (~85 Gb) greatly outweighs that of the long reads (4 Gb). As hybrid assembly hasn't been very successful so far, is it possible for Nanomotif to use an assembly generated with short reads as input?
The text was updated successfully, but these errors were encountered: