Entering edit mode
2.9 years ago
Neel
▴
20
Hi, I am trying to run FastANI and it run perfectly but it produced blank/Empty output even i tried at AAI amino acid level still result are same, what i can do ?
fastANI -q /home/neel@m95/Desktop/AMR/annotated/fna/1.txt --rl /home/neel@m95/Desktop/AMR/refgenome/2.txt -o output_2.txt
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Reference = [GCA_000006765.1_ASM676v1_genomic.fna]
Query = [/home/neel@m95/Desktop/AMR/annotated/fna/1.txt]
Kmer size = 16
Fragment length = 3000
Threads = 1
ANI output file = output_2.txt
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INFO [thread 0], skch::main, Count of threads executing parallel_for : 1
INFO [thread 0], skch::Sketch::build, window size for minimizer sampling = 24
INFO [thread 0], skch::Sketch::build, minimizers picked from reference = 501302
INFO [thread 0], skch::Sketch::index, unique minimizers = 477392
INFO [thread 0], skch::Sketch::computeFreqHist, Frequency histogram of minimizers = (1, 458218) ... (18, 1)
INFO [thread 0], skch::Sketch::computeFreqHist, consider all minimizers during lookup.
INFO [thread 0], skch::main, Time spent sketching the reference : 1.04382 sec
INFO [thread 0], skch::main, Time spent mapping fragments in query #1 : 0.000250891 sec
INFO [thread 0], skch::main, Time spent post mapping : 1.33e-06 sec
INFO [thread 0], skch::main, ready to exit the loop
INFO, skch::main, parallel_for execution finished
Thank you
Actually i wanna do pan genome comparison. Thank you for your time, it will be very helpful for me.