Next Generation Sequencing Products & Reviews

Confidently analyze multiple somatic variants with a flexible, automated NGS workflow

BioIVT provides isolated exosomes from a variety of human, animal, and plant sources, as well as custom characterization and in vitro assays investigating function and potential therapeutic benefit.

SimpliFY Your Clean Ups. Microlab PuriFY offers a compact, standalone solution for automated nucleic acid bead-based clean-up for NGS library preparation and PCR, enabling scientists to spend less time of tedious, repetitive tasks and more time concentrating on their vital research.

Space-Saving, On-Deck Fluorescence Measurements. The Fluoreye mobile fluorescence reader is operated by a 1000 µL pipetting channel, moving to and measuring samples in 96-well flat-bottom plates.

Stop gambling on cycle numbers. The icon96 uses iconPCR™ technology with AutoNorm™ software to provide real-time fluorescence feedback in each of 96 independent wells, preventing under-amplification dropouts and over-amplification artifacts—delivering balanced, sequencing-ready libraries without manual quantification or normalization.

The icon16™ brings AutoNorm™ adaptive amplification to lower-throughput NGS workflows, with up to 16 samples at a time. Designed for labs that refuse to compromise on data quality, it delivers per-well real-time fluorescence monitoring and automatic library normalization in a compact, benchtop footprint.

Sapio LIMS for clinical diagnostics enables your lab to quickly design, deploy, and automate end-to-end workflows to meet your lab’s exact needs. Including a physician portal; automated accessioning and order processing; multithreaded, out-of-the-box, no/low-code configurable workflows; simple and sophisticated automation rules; and streamlined report generation.

A complete targeted resequencing solution for a wide range of applications, with fast integrated workflow and options for custom and fixed enrichment panels.

A fast, integrated workflow for preparing libraries for use in a wide range of sequencing applications.

Illumina 5-base solution for methylation and variant detection

The NovaSeq X and NovaSeq X Plus Sequencing Systems deliver extraordinary throughput and accuracy to perform data-intensive applications at production scale.

Expansive application breadth and operational simplicity with proven performance

The first CE-marked IVD kitted solution for comprehensive genomic profiling (CGP) of DNA and RNA variants, plus MSI and TMB, for multiple solid tumor types.

Fluorescent Annexin V conjugates that are optimized for bright and low background staining of extracellular vesicles for flow cytometry.

Automated Purification of High-Quality Total RNA with an Enhanced miRNA Enrichment

BisCap® Human CpG Island Panel is targeted for detection of methylation status of 27,000 CpG island and also covers 13 commercial methylation markers. The panel could be widely used in methylation marker screening, early tumor screening, early detection, and etc.

Based on tumor-informed assays, combined with independently developed hybridization capture systems and high-throughput MRD Panel synthesis, we have launched a comprehensive MRD hybridization capture reagent set—including hybridization capture reagents, blocking sequences, and capture beads. Paired with free customized MRD Panels, this solution delivers a cost-effective and highly stable MRD detection protocol, promoting the p…

TargetSeq® Universal Blocking Oligo series products are used to block self-ligation of adapters to reduce non-specific adapter interaction during probe hybridization and thus to increase data utilization. iGeneTech offers 2 versions of universal blocking oligo for different library input in hybridization workflow, i.e., TargetSeq® Universal Blocking Oligo and TargetSeq® Eco Universal Blocking Oligo for up to 6 μg and 3 μg libr…

IGT® Adapter & UDI Primers is a series of adapter & unique dual-indexed primer kits used for NGS library construction of dsDNA, ssDNA and methylation DNA. iGeneTech provides 384 combinations of different UDI primers for high-throughput sequencing in a single lane, which reduces the false-positive rate caused by the index contaminations due to index hopping. For MultipSeq® library construction and low-frequency mutation tests,…

iGeneTech® owns the independently developed TargetSeq® hybridization capture sequencing technology and IGT® Oligo Pools synthesis platform, which enable the design of products targeting exon regions and offering comprehensive solutions for whole-exome sequencing across various species. As of now, we have successfully developed panels for the whole exomes of mice, rats, dogs, pigs, cattle, sheep, chickens, and more all of which…

TargetSeq® Human HLA Panel and TargetSeq® Human MHC Panel are HLA gene detection products based on TargetSeq® hybridization capture technology developed by iGeneTech. These panels are highly efficient in capturing the polymorphic region and combined with NGS technology to achieve high-precision typing of the HLA gene at 6 sites, and can be widely used in the field of immunology research.

IGT® Enzyme Plus Library Prep Kit V3 provides you a fast and streamlined workflow for NGS library preparation with enzymatic fragmentation strategy. The kit enables tunable fragmentation for different insert sizes according to experimental requirements and is suitable for genomic DNA and FFPE DNA samples with ranged sample input to generate satisfied yield. To achieve good performance with increased sequencing efficiency, IGT®…

TargetSeq One® Hyb & Wash Kit v3.0 is a fully upgraded version of the TargetSeq One® Hyb & Wash Kit. This upgrade has greatly simplified the reagent composition and operation process, reducing the operation time by more than 1 hour; meanwhile, in terms of product performance, the uniformity and capture efficiency have been significantly improved to a brand-new level. This means that the test results are accurate and reliable,…

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-cus…

The Twist FlexPrep™ UHT Library Preparation Kit streamlines ultra-high throughput sequencing by integrating Normalization by Ligation™ technology, enabling efficient sample processing for population studies and agrigenomics.