Find out more about the application of 42Genetics solutions in the following fields

Oncology applications


Tumor specific mutations are detected using somatic calling to find the true differences between a germline and a tumor sample...

Learn more
Reference Migraton applications

Reference Migration

The enormous momentum in human genomics results in continuous new insights and development of techniques for genomic...

Learn more
Human Genetics applications

Human Genetics

The application of Whole Genome Sequencing within Human Genetics is steadily moving from research to clinic...

Learn more
Population Genetics applications

Population Genetics

Modern NGS platforms can produce tens of thousands genomes per year, enabling large-scale Population Genetics...

Learn more
Agrigenomics applications


Plant genomics can be easily referred to as ‘a very special breed’. This is caused by the size of the genomes...

Learn more
Rare Diseases applications

Rare Diseases

The use of Next Generation Sequencing in the field of rare diseases is all about finding rare candidate mutations...

Learn more
42Genetics Solution

42Genetics provides a modular high performance NGS secondary analysis solution.

Our solution creates a reliable bridge between NGS data streaming from the sequencer (FASTQ or unaligned BAM) to detailed genetic interpretation and reporting solutions.

Read more

The benefits of 42Genetics solutions

speed icon

From FASTQ to VCF in less than 20 minutes.

accuracy icon

Highly accurate and precise alignment and variant calling.

ease of use icon
Ease of use

All-in-one solution simple workflow and flexible deployment.

filesize icon

Twentyfold storage footprint reduction of aligned read files.

Who we work with