Grandomics specializes in third-generation sequencing technology to provide molecular diagnostics and carrier screening for single-gene diseases. Their platform enables accurate detection of genetic variations and complex genomic regions, facilitating precise diagnosis and research in genetic disorders.
Funding
$15M raised to dateRaised to date based on public sources. This may differ from the amount the company actually raised and is based only on what is publicly available on the internet.
Founders
Product
Problem
Existing sequencing technologies often struggle with long repetitive regions and complex genomic variations, leading to incomplete or inaccurate genome assemblies, which hinders precise molecular diagnostics and comprehensive carrier screening for single-gene diseases.
Solution
Grandomics leverages third-generation sequencing to overcome the limitations of previous technologies, providing comprehensive molecular diagnostics and carrier screening for single-gene diseases. The company's platform generates ultra-long sequencing reads, enabling accurate detection of genetic variations and resolution of complex genomic regions, including continuous repeats and large fragment duplications. By providing a more complete and accurate representation of the genome, Grandomics facilitates precise diagnosis, accelerates research into genetic disorders, and enhances the understanding of genetic diversity. Their technology offers complete genome sequencing, accelerating the discovery of genetic resources and the implementation of genomics applications in animal and plant breeding.
Target Audience
Grandomics serves researchers and clinicians in molecular diagnostics, carrier screening, and genetic disorder research, as well as those in the agriculture industry.
Features
- Generation of ultra-long sequencing reads to span repetitive or duplicated genomic regions
- Comprehensive genome sequencing for complete genetic diversity analysis
- Advanced functional annotation and diversity classification
- Detection of dynamic mutations with higher efficiency and precision
- Custom high-performance analysis servers with long-read databases and proprietary algorithms
- Services include:全基因组Survey, 动植物基因组de novo, 全基因组重测序（二代/三代）, 泛基因组, Nanopore全长cDNA测序, Nanopore直接RNA测序, Iso-Seq全长转录组, RNA-Seq, 空间转录组, 单细胞转录组, 纳米孔单细胞全长转录组测序, 细菌基因组完成图, 真菌基因组近完成图, 宏基因组, 16S/18S/ITS扩增子测序, 基因组表观组学研究, 蛋白质组学, 线粒体/叶绿体基因组完成图, 人类基因组结构变异检测, 全基因组甲基化, 三代全外显子组测序, 微生物组