Next generation sequencing
Perform sequencing and analysis of nucleic acids. Study genetic and epigenetic information using NGS.
PacBio creates advanced sequencing systems, providing the most complete and accurate view of genomes, transcriptomes, and epigenomes.
OncoDNA provides comprehensive biomarker test to help oncologists determine the best treatment for patients with advanced-stage solid tumors.
Arima Genomics enables the study of 3D genomics and provides a unique approach to the sequence, structure, and regulatory environment of any genome.
enGenome’s software allows for accurate and timely diagnosis of rare diseases, ensuring high accuracy in the interpretation of genomic variants.
A provider of sequencing and diagnostic services.
SeqWell enables the creation of balanced library pools without the need for sample or library normalization. The fast and simplified workflows multiplex 100 to 1,000 samples for loading in a single sequencing run, allowing for increased overall sequencing throughput.
A complete solution for library preparation for next-generation sequencing (DNA, RNA short-read sequencing).
Hedera Dx provides cutting-edge liquid biopsy solutions that improve patient experience and response to treatment as well as healthcare professionals’ experience, while facilitating the discovery and development of other revolutionary treatments in precision oncology.
RealSeq® is a new method of small RNA library preparation that almost eliminates bias in next-generation sequencing (NGS). This technology addresses the issue of commonly used library preparation kits that lead to inadequate detection of many miRNAs, some up to 10,000 times less.
