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Dear Isaac,
I would like to apply mccortex on a large scale resequencing project. (~400 individuals, 1GB genome size),
I read through the wiki, and here is what I think a possible workflow might look like
- Build graphs for each sample and reference with one chosen kmer size
- Clean each of the graphs
- Merge the clean graphs
- Read threading to produce link files
- Clean link files
- Merge the clean link files
- Call the variants
Do you have any suggestion about the workflow or is there any pitfall I need to be aware of?
Thank you so much.
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