IDT Signs Strategic Partnership with Chinese Medical Sequencing Firm ChosenMed

Partnership strengthens IDT’s position as an NGS leader in China

1 Jul 2019
Georgina Wynne Hughes
Editorial Assistant

Industry news

Integrated DNA Technologies (IDT) has announced that it has entered into a strategic cooperation with ChosenMed Technology (Beijing) Co., Ltd (ChosenMed), a medical sequencing firm focused on personalized medicine and transformation healthcare in China. As part of the collaboration, IDT will provide its market-leading NGS enrichment products* for cancer sequencing to ChosenMed, and also help to enhance its scientific research and development capabilities. The two parties will work together on the research and development of large pan-cancer panels as part of the Cancer Genome Atlas of China (CGAC) project, focused on the future of Chinese cancer diagnosis.

IDT’s NGS products* are popular within the medical sequencing community and this partnership demonstrates a growing adoption of the company’s NGS solutions in clinical and translational markets.

The CGAC project, led by a Chinese government department that provides national standards for the registration of medical devices, has identified a clinical need for a large pan-cancer panel to standardize cancer diagnosis for Chinese patients. Working to develop and ultimately register this, ChosenMed sought to align with the high-quality NGS product and expertise provider, and were impressed with the data quality and fidelity that IDT’s popular, individually-synthesized and quality-controlled xGen®* NGS enrichment probes provide.

The partnership has been formed to facilitate cooperation and collaboration between the two companies, who will seek to train and educate each other, and work jointly towards the goal of the initiative - to standardize cancer diagnosis across China.

Trey Martin, President of IDT commented, “IDT’s mission is to continually advocate for genomics research, with the ultimate aim of helping to improve people’s lives. ChosenMed is committed to leadership in the field of cancer precision medicine, and this strategic cooperation allows our two organizations to leverage expertise in a joint effort to address future clinical needs. ChosenMed has recognized that our high-quality NGS products can help translate data into actionable treatment for patients. Together we will enable that transition from the bench to the clinic.”

Through this partnership and the CGAC project, ChosenMed and IDT will work together to build and develop future standards of NGS-based cancer diagnosis and, ultimately, treatment in China.

*Research use only, not for diagnostic use.

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Genome AnalysisGenomics, the study of genomes, includes functional genomics, evolutionary genomics and comparative genomics. There are many genomic technologies such as DNA sequencing of whole genomes, computational biology and bioinformatics. DNA and nucleic acids must be isolated and concentrated from cells for analysis with kits, automated analyzers and software. Other useful technologies for studying genomics include PCR, microarrays and electrophoresis.Clinical GeneticsMolecular Genetics covers the analysis of hereditary genetic disease and chromosomal abnormalities. Genetics can be analysed using DNA, RNA, and protein microarrays, PCR, RT PCR and DNA sequencing. Genetic equipment includes genetic workstations, thermal cyclers, cooling blocks and electrophoresis products. Diagnostic kits are used for DNA / RNA extraction and purification.Next Generation SequencingNext-generation sequencing (NGS), also known as whole-genome sequencing, high-throughput sequencing and massive parallel sequencing, produces and analyses thousands to millions of nucleotide sequences at once. Sequencing systems operate via varying technologies depending on the manufacturer, including sequencing by synthesis, ligation, pyrosequencing, ion semiconductor and single-molecule real-time sequencing. For NGS, library preparation is paramount to successful sequencing. In this section, explore a range of library preparation kits, from targeted, amplicon-based or hybridization-based kits including epigenomic, transcriptomic and genomic workflows to fragmentation kits. Find the best next-generation sequencing products in our peer-reviewed product directory: compare products, check customer reviews and receive pricing direct from manufacturers.Cancer DiagnosticsThere are a wide variety of diagnostic tests for cancer available, and this range continues to expand as our knowledge of cancer improves. Current diagnostic methods include biopsy, imaging and blood tests for known biomarkers. New methods in research development include liquid biopsies and cancer breathalyzers.NGS SoftwareClinical NGSNext Generation Sequencing (NGS) refers to the use of massive parallel sequencing of multiple small fragments of DNA. This high-throughput genomic analysis yields enormous amounts of sequence data, which if appropriately analyzed could have huge potential for clinical laboratories. For this to happen there are technique and bioinformatic hurdles to be overcome.GenomicsGenomics is the study of genomes, focusing on the sequencing, analysis, and interpretation of genetic material. It is key in understanding genetic diseases, evolutionary biology, and personalized medicine. Techniques like next-generation sequencing (NGS) are commonly used in genomics research. Browse our peer-reviewed product directory to find the best genomics tools, compare products, check reviews, and get pricing directly from manufacturers.Genome SequencingGenome sequencing involves determining the complete DNA sequence of an organism's genome. It provides crucial information about genetic variations, mutations, and diseases. Advances in sequencing technologies, such as next-generation sequencing (NGS), have accelerated research in genomics, diagnostics, and personalized medicine. Explore genome sequencing tools in our peer-reviewed product directory; compare products, check reviews, and get pricing directly from manufacturers.Precision MedicinePrecision medicine refers to the idea of customized healthcare, where medical decisions and treatments are tailored to the individual patient. Molecular diagnostics, companion diagnostics and Next Generation Sequencing (NGS) play a pivotal role in this approach. Cancer ResearchAlthough cancer is often referred to as a single condition, it actually consists of more than 100 different diseases. Microscopy, mass spectrometry, high throughput sequencing and flow cytometry are some of the most common techniques employed in cancer research labs.
IDT Signs Strategic Partnership with Chinese Medical Sequencing Firm ChosenMed