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Making sense of the world’s genomic data.
Revolutionizing long and short read whole genome, whole exome, transcriptomic, and proteomic sequencing through a proprietary compression algorithm which delivers smaller, faster, cleaner data. The 42Genetics platform addresses the challenges of massive data generation and the required processing power in genomic analysis.
About usProducts
Find out more about the application of 42Genetics solutions in the following fields
Oncology
Tumor specific mutations are detected using somatic calling to find the true differences between a germline and a tumor sample...
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Reference Migration
The enormous momentum in human genomics results in continuous new insights and development of techniques for genomic...
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Human Genetics
The application of Whole Genome Sequencing within Human Genetics is steadily moving from research to clinic...
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Population Genetics
Modern NGS platforms can produce tens of thousands genomes per year, enabling large-scale Population Genetics...
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Agrigenomics
Plant genomics can be easily referred to as ‘a very special breed’. This is caused by the size of the genomes...
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Rare Diseases
The use of Next Generation Sequencing in the field of rare diseases is all about finding rare candidate mutations...
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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 moreThe benefits of 42Genetics solutions
SMALLER
42Genetics significantly reduces the size of a BAM file on average
FASTER
Compared to competing hardware/ software solutions such as DeepVariant, 42Genetics is faster by over 2 days per genome. 42Genetics calls files with a single node:
CLEANER
42Genetics remaps your data allowing for quick updates to legacy reference sets while still integrating into customers downstream analysis pipeline on-premises or in the cloud. 42Genetics delivers highly accurate and precise alignment and variant calling.
