Open deyuanyang opened 1 year ago
Hi @deyuanyang:
Thank you for using cuttlefish! I see that you're using FASTQ inputs---in that case, you need to pass the --read
argument. Besides, I also see that you're using the -f 1
argument, which specifies a specific output format among a few ones. When working with read sets, cuttlefish can only output the assembled maximal unitigs (i.e. contigs) for now, and so the -f
option is not applicable.
I think for your example datasets mentioned above, you can use the following command:
cuttlefish build --seq <file-1> --seq <file-2> -k 33 -o <output-file> -t 8
Let me know if that solves the problem(s). Regards!
Hi,
It's a perfect soft. When I used it to assemble my data, I could not understand the --read parameter, if I have data like R1_fq.gz, and R2_fq.gz, how to use it? It can use like Spades. -1, -2, -U for input data?
Best wishes, Deyuan