Variant calling and filtering

Qlucore Omics Explorer is a next-generation bioinformatics software for research in life science, biotech, food and plant industries, as well as academia. The powerful visualization-based data analysis tool with inbuilt powerful statistics delivers immediate results and provides instant exploration and visualization of big data including variants in NGS data.     

genome browser

Variant calling and analysis 

The Qlucore Omics Explorer NGS module includes rich functionality for variant analysis. The genome browser works smoothly with the user friendly and flexible variant filters. Set one or several filters and directly inspect the results with a focus on those parts of the genome fulfilling the criteria.

Use either the inbuilt variant caller, Samtools, or supply variants called with another caller. The vcf file format is supported.

Combine the variants found in your data with findings in databases and populations by importing additional vcf files.

Does it work on my data?

Answer the four quick questions below and find out if you can use Qlucore on your data. 

For more details about supported data formats and data import see Data Import or Contact us with questions.

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