Making sense of the worlds genomic data.
The value of genomic data is tremendous, yet it is a mammoth task to master these large data sets. From small labs to large nationwide programmes, panel tests to full genome analysis and in the search to detect decisive markers and rare variants, we take care of it.About usProducts
Find out more about the application of 42Genetics solutions in the following fields
Tumor specific mutations are detected using somatic calling to find the true differences between a germline and a tumor sample...Learn more
The enormous momentum in human genomics results in continuous new insights and development of techniques for genomic...Learn more
The application of Whole Genome Sequencing within Human Genetics is steadily moving from research to clinic...Learn more
Modern NGS platforms can produce tens of thousands genomes per year, enabling large-scale Population Genetics...Learn more
Plant genomics can be easily referred to as ‘a very special breed’. This is caused by the size of the genomes...Learn more
The use of Next Generation Sequencing in the field of rare diseases is all about finding rare candidate mutations...Learn more
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
From FASTQ to VCF in less than 20 minutes.
Highly accurate and precise alignment and variant calling.
Ease of use
All-in-one solution simple workflow and flexible deployment.
Twentyfold storage footprint reduction of aligned read files.
What people say about us
42Genetics CNV calling tool...— Mike Furness (@TheFirstNuomics) June 7, 2018
Validation of an ultra-fast CNV calling tool for Next Generation Sequencing data using MLPA-verified copy number alterations https://t.co/nJqWOOjMoo