Sequencing Services Products & Reviews

CD Genomics provides complete plasmid DNA sequencing service, and their improved bioinformatics pipelines are available to perform de novo assembly with no reference required.

Get the most complete genomic information of any organism with whole genome sequencing (WGS). Macrogen Europe’s fast, high-quality WGS services provide the most comprehensive tool for detecting genetic abnormalities such as single nucleotide polymorphisms (SNPs), indels, copy number variation (CNV) and structural variants (SVs).

Illumina 5-base solution for methylation and variant detection

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,…

In-depth understanding of complete genome in human, aninal, plant and microbe with end-to-end services.  

Sequencing only service for customer-premade libraries at different read lengths and capacities to suit any cost, project scale and turnaround with the world-leading, powerful, and sophisticated sequencing platforms (Illumina, Pacbio, and Oxford Nanopore). 

16S/18S/ITS rRNA amplicon metagenomic sequencing employs universal primers to target specific regions to identify the phylogeny and taxonomy from complex microbiomes.

Single cell RNA sequencing uncovers the complexity of cellular diversity to employ the study of unusual cell types, cell-lineage associations, and samples of heterogeneous nature with 10x Genomics technology.

Long Read Sequencing (LRS) service employs cutting-edge technologies such as Oxford Nanopore and PacBio platforms for decoding complex genomes, completing transcriptomes, exploring metagenomes, and investigating structural variations with unmatched precision.  

RNA sequencing is applied for in-depth analysis of whole transcriptomes, encompasses coding and non-coding RNAs (long ncRNA, small RNA, and circle RNA,etc.) for diverse research needs.  

Whole exome sequencing allows for sequencing human and mouse exomes in an array of panel options, which facilitates research contexts and clinical contexts.

Shotgun metagenomic sequencing is designated to sequence the total genomic DNA from environmental samples without the prior isolation and cultivation of individual species. The services are applied for studying the rich genetic repertoire of microbial communities with taxonomy information, and for studying system evolution, gene function, and metabolic network of environmental microorganisms.

Novogene provides Whole Genome Bisulfite Sequencing (WGBS), Reduced Representation Bisulfite Sequencing (RRBS), Chromatin Immunoprecipitation Sequencing (ChIP-seq), RNA Immunoprecipitation Sequencing (RIP-seq), and Assay for Transposase-Accessible Chromatin Sequencing (ATAC-seq), tailored for both bulk and single-cell samples.

Revvity Ultrarapid Whole Genome Sequencing: Get a final report for urWGS in just 5 days!

OGT can help you get straight to the variant of interest with whole exome or custom targeted sequencing services. Genefficiency™ targeted sequencing services are designed to be different, leading you all the way from project conception to high-quality results. Our expert and comprehensive project design and analysis solutions — incorporating Agilent SureSelect, Illumina HiSeq 2000 and OGT-developed software platforms — are ta…

A high-quality RNA sequencing service designed to deliver cost-effective and rapid access to meaningful transcriptomics results. The Genefficiency™ RNA-Seq Service from OGT provides a new level of assay customisation to ensure each experiment is fully optimised to suit your specific study objectives. At OGT we understand the time and effort it takes to generate good quality RNA and how precious your samples are. Whether you a…

Discover the diversity of microbial communities

An unprecedented view into transcriptional heterogeneity