About
iGeneTech Bioscience, founded in Beijing in 2014, is a biotechnology company focusing on the development and supply of target gene "reading" and "writing" solutions with our three proud technology platforms: NGS hybridization capture, multiplex PCR and high-throughput DNA synthesis. We provide catalog and customized NGS target enrichment panels, NGS reagents and kits, OEM and CDMO services and automation solutions to thousands of customers from various fields including healthcare, agriculture, microbiology and academic research. We've set high quality standards to our NGS products, and our quality management system has received ISO 13485:2016 and ISO 9001:2015 certifications. https://www.igenetech.com/
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AIExome® Human Exome Panel V5 is designed based on human reference genome GRCh38 and GRC. It covers about 34.69 Mb CDS region, and the probe coverage size is only 48.17 Mb, ensuring maximum coverage of the protein-coding region. AIExome® V5 has also been optimized for probe coverage of reference genome patches, high repeat regions and high GC content regions. AIExome® V5 series has 3 different versions and are open to semi-customization, where customers can add or enhance probes for regions of interests based on standard AIExome® V5.
Contact
- Headquater:
No. 1A Chaoqian Road, Science and Technology Park, Changping District, Building 13, Beijing, Beijing 100000, CN
OEM Services
Overview
iGeneTech is experienced in manufacturing and delivering customized panels and reagent kits.
Advantages
From Materials to Products
iGeneTech has supplied over 100 of reagent kits and near 2000 customized panels to near 1000 customers with high quality in recent years.
From Materials to Products
Customized OEM Available
iGeneTech also offers OEM services to target sequencing reagent kits and liquid-handling workstations to meet the diverse requirement of customers.
Customized OEM Available
Strict Quality Management
Based on iGeneTech's GMP-compliant workshop and quality management system certified by ISO13485:2016, the whole manufacturing process is traceable with documented manufacture records and QC reports.
If you want to know more custom ngs, please visit our website.
As one of next generation sequencing companies, we will do our best to meet all the needs of customers.
NGS Solutions
Our NGS Solutions encompass OEM Services and Lab Services, designed to meet diverse research needs. We offer tailored NGS target enrichment panels, reagents, and kits, ensuring high-quality and reliable results. Our automation solutions streamline workflows, enhancing efficiency and accuracy in healthcare, agriculture, microbiology, and academic research.
If you want to know more about sanger sequencing services, please visit our website.
Fast Library Prep Kit
Overview
The IGT® Fast Library Prep Kit v2.0 is a rapid library construction kit for fragmented dsDNA. It offers a fast and user-friendly alternative to a quick 16S NGS library prep kit, especially for applications based on A-T ligation, with a simple workflow and suitable input range from 1 ng to 500 ng.
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Advantages
Suitable for low input amount and low-quality samples.
Simple and rapid workflow, only requires 3.5 h to finish the library construction.
Combined with self-developed UDI and UMI technologies, it can effectively reduce data crosstalk and meet the needs of low-frequency variation detection.
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Performance
Superior Performance for Low Input Amount Samples
The IGT® Fast Library Prep Kit v2.0 has a high library conversion rate that leads to a higher library yield even with low input amount compared to major competitors.
Superior Performance for Low Input Amount Samples
Excellent Performance for Low-quality Samples
Compared to major competitors, the IGT® Fast Library Prep Kit v2.0 can effectively improve the library quality even with the low-quality samples like FFPE, so as to obtain reliable sequencing results.
Excellent Performance for Low-quality Samples
Higher Molecular Recovery Rate
The IGT® Fast Library Prep Kit v2.0 can effectively reduce library distortion and sequence errors to ensure the high accuracy of the sequencing results.
Compared to major competitors, the kit can obtain 30% to 50% higher sequencing depth after SSCS and DCS.
Higher Molecular Recovery Rate
High Repeatability for Stable Performance
The repeatability test results using the IGT® Fast Library Prep Kit v2.0 showed that the mutation rates detected (VAF ≥ 0.5%) has a superior consistency, indicating the kit is able to achieve accurate and reliable results.
High Accuracy for Low-Frequency Mutation Detection
With UMI-UDI adapters, the IGT® Fast Library Prep Kit v2.0 can effectively be used for low-frequency mutation tests.
Tests using reference standard with known 8 mutations with VAF of 0.5% showed that all 8 mutations were successfully detected with highly accurate VAFs.
If you want to know more about rna sequencing service, please visit our website.