Software
supernova
- Does supernova --maxreads downsample reads randomly?
- How does Supernova measure the repetitive fraction of the genome?
- Can Supernova combine multiple libraries in an assembly?
- Why does molecule size not seem to correlate with Supernova assembly quality?
- Where can I find the effective median coverage in the Supernova logs?
- Is there a way to fill in a gap in our Supernova assembly that falls within our region of interest?
- Where can I find, and how should I cite, the Supernova publication?
- Are there any parameters I can adjust to optimize the performance of Supernova?
- Can I use Supernova to assemble a polyploid or haploid genome?
- How do I specify memory and cores for Supernova?
- Can Supernova run with more than 28 cores?