DNA Sequencing Sequencing Services Products & Reviews

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).

mRNA sequencing (mRNA-seq) is a potent method for gene expression exploration, it unveils mRNA dynamics, different gene expression and regulatory mechanisms with precision.

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

New insights from beyond the sequence

Revolutionary, cost-effective genome assembly

Established solid tumour gene panel

Single base-pair, high-throughput solution for analysis of methylated DNA regions

Comprehensive services for DNA enrichment and profiling of genomic regions marked by DNA methylation or DNA methyl variants

Fastest, most efficient methylated DNA enrichment method on the market

Comprehensive services for DNA enrichment and profiling of genomic regions marked by DNA methylation or DNA methyl variants

Transcriptome profiling by RNA-Seq

Insights into the diversity of microbial communities

Next-generation sequencing research services for SARS-CoV-2 variant surveillance.

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.