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:scissors: :zap: Rapid haploid variant calling and core genome alignment

Results 162 snippy issues
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After running snippy on multiple isolates, with command snippy-multi , i have run recombination detection tool as given: %run_gubbins.py -p gubbins clean.full.aln % snp-sites -c gubbins.filtered_polymorphic_sites.fasta > clean.core.aln % FastTree...

I'm calling variants from 10 samples using one reference fasta for all. The samples are from the same strain. One sample is WT and the others were under different stress...

help wanted

Hello, I have already used snippy and snippy-multi in my previous work. I have recently installed snippy into a new PC but I think snippy-multi is not exported. Whenever I...

Hi Torsten Seemann, Thanks a lot for developing and maintaining snippy! I'm using your tool to study deletions. While investigating the output for deletions I realized that I ether don't...

Running one sample at a time works OK, can't create runme.sh $snippy-multi input.tab --report --html --cpus 7 --ref /home/shawndy/Biomatics/snippy/C01_assembly.fasta > runme.sh causes: ERROR: [C01_/home/shawndy/Biomatics/snippy/C01/Sample1.R1.fastq_/home/shawndy/Biomatics/snippy/C01/Sample1.R2.fastq] missing read/contig data: C01 /home/shawndy/Biomatics/snippy/C01/Sample1.R1.fastq /home/shawndy/Biomatics/snippy/C01/Sample1.R2.fastq...

How should one cite snippy?

![image](https://user-images.githubusercontent.com/91398760/134790469-c70cc153-6a05-4143-8e12-f2def7e19e40.png)

I was using Snippy and I recommend the use of this software. Great Job! When I ran it with a reference in gbk file format Snippy split it into Fasta+GTF...

Hello, @tseemann my friends tried to make a loop on output that we got from running bbduk on snippy code example provided by you but it won't work the output...

I have run 25 samples on snippy-multi and individually all runs seem ok but in core.txt only shows 1 snp for the last file.