Macrogen Europe B.V offers DNA sequencing using state-of-the-art robotics and instrumentation to generate high quality sequence data at affordable prices.
We have successfully sequenced countless samples of PCR products and plasmids from clients all over the world, and our DNA sequencing services are highly rated for their turnaround time, quality of results, and competitive prices.
EZ-seq is designed to bring easiness and simplicity to your daily DNA sequencing process. EZ-seq and EZ-Bag are prepaid barcode services for premixed samples.
Macrogen sequencing service is provided by 3730XL DNA analyzer(AB,USA) and BigDye v3.1(AB,USA). All of the process from sample receipt to data dispatch are done under the tight control of our own LIMS which is developed by us.
Eco-seq is the most flexible and easiest barcode service for scientists who could make a short-cut workflow in preparation of samples. ECO-Seq is a prepaid barcode service for no mixed samples. Option for purification available.
Oligos - Fragment Analysis - Difficult Sequencing -Primer Walking – 16sRNA service – ITS service – PCR Amplification
Today, Next Generation Sequencing (NGS) technology has made it possible to decode the entire human genome in as little as few days; revolutionizing the approach to study the genome. NGS technology applications enable unprecedented scalability and touch on all areas of genetic research. These contemporary sequencing methods are much more sensitive, enabling clinicians and researchers alike to discover a greater volume of submicroscopic views of our genomes.
Whole genome sequencing (WGS) is the process of determining the complete DNA sequence of an organism's genome, and the most comprehensive tool for detecting single nucleotide variants, insertions, deletions, copy number changes and structural variants.
Whole exome sequencing (WES) is a targeted approach that makes possible to identify variations in the protein coding part in a genome. This can be especially valuable because most known genetic variants occur in exons.
Cancer Panel Sequencing characterizes fast-track oncology data by surveying either hotspot mutations or whole exome sequences of oncogenes and tumor suppressor genes. Macrogen provides various enrichment methods, as well as helps customization of a panel for your genes of interest.
A transcriptome is a collection of all the transcripts present in a given time point. By analyzing the entire collection of RNAs or transcriptomes, researchers can determine when and where each gene is turned on or off in the cells and tissues of an organism.
If traditional transcriptome sequencing (also called bulk RNA sequencing) is the way to see the average gene expression in different cells, then Signal Cell RNA Sequencing can analyze thousands of transcription bodies simultaneously at a single cell level, so we can see the difference in gene expression values for different cell types.
Epigenome sequencing confirms that the function of a certain gene is expressed by external environmental factors. Methylation of DNA and acetylation of histone protein are the most representative epigenetic control mechanisms for the transcription of genes.
Metagenome sequencing is a method of identifying microbial communities in different environments including the ones that cannot be cultured in laboratory setting. It is used primarily to analyze the distribution and types of bacteria and fungi, and to identify their interactions and roles.
Get familiar with our overall workflow, learn how to prepare samples, and how to ship your samples to Macrogen.