Omixon Variant Toolkit
The Toolkit includes highly accurate tools for detecting micro indels and SNP.
It offers a solution to map color reads with a moderate distance (5-30% sequence divergence) from reference genomes. It poses no restrictions on the size of the reference database, which, combined with its high sensitivity, makes the Variant Toolkit well-suited for metagenomic sequencing projects.
The Toolkit also offers another unique feature - a consensus building tool that takes the read quality scores into account, using a well-defined probablistic model. This leads to a significantly improved variant calling accuracy.
More details
How many indels are you missing?
Mind the gap
Variant Toolkit’s user benefits:
- The Omixon Variant Toolkit is your best chance not to miss the structural variation you are looking for
- Exceptional performance
- Very simple to run
- Intuitive parameters
- Fastest return of results due to elastic infrastructure of Amazon
- High availability and reliability
- Reporting calculated structural variations with statistical significance
- Cost efficient
- Reads both color space and letter space in FASTQ format
