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Benchtop sequencer ease-of-use with production-scale power in a single platform
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Assay targeting multiple somatic variant types from plasma, including TMB and MSI
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Fast library prep, optimized for small genomes, PCR amplicons, and plasmids
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CNV analysis on somatic samples, population-level cohort analysis
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Fast, high-quality, sample-to-data services such as RNA and whole-genome sequencing
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NGS offers a universal, hypothesis-free research method for use with viruses, bacteria, or parasites
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One mother’s quest for a diagnosis
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Expanded portfolio enables comprehensive genomic profiling from blood and tissue
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Sequence virtually any small genome and make new discoveries with scalable throughput
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Contributing to a sustainable environment and food supply
An economical tool for genetic screening of large global populations
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In-lab aneuploidy screening solution for accurate NIPT results in 26 hours
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Many more diseases could potentially be treated by controlling the expression of abnormal and normal genes
Assay targeting multiple variant types, including tumor mutational burden (TMB) and microsatellite instability (MSI), even from low-quality samples.
Cost-efficient flexibility for new and emerging applications.
Scalable throughput and flexibility for virtually any genome, sequencing method, and scale of project.
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