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Description
Hi!!!!
Thank you very much for your tool!
I’m currently working with metagenomic reads, and now, with my FASTA files grouped by species, I’m trying to generate a consensus assembly with Flye (since afterwards I want to map my reads back to the consensus — my project is focused on genetic variability). However, I’ve been running into some issues, and I would really appreciate your advice.
For example, one of my FASTA files for a given species has around 309,160 reads (which is quite a lot). I have been using the following command:
nohup flye --nano-raw Akkermansia_muciniphila.reads.fa
--out-dir flye_1_octubre
--threads 32
--genome-size 6k
--meta > flye_1_octubre.log 2>&1 &
With this command, the process is taking a very long time. Is this expected, or would you have any suggestions to improve it?
I would love to hear your recommendations. Thank you in advance!