Choose efficient, cost-effective sequencing focused on protein-coding regions. Our whole exome sequencing (WES) service lets you choose from a range of industry-leading library prep kits for hybridization enrichment – including those from Agilent and Twist – to make sure you get the reliable libraries you need.
Create an account on our ordering platform and submit orders right from your lab chair.
Whole exome sequencing (WES) is a targeted approach that makes it possible to identify variations in the protein-coding part of a genome. In humans, only around 1% of the genome consists of exomes. However, most disease-related genetic variants occur in exons, making these regions crucial to many genetic studies.
Because the sequenced region is narrowed down from gigabasepairs to megabasepairs, sequencing throughput required per sample per analysis is much smaller. This makes exome sequencing unbeatable in terms of precision and economy and method of choice for many researchers and clinicians.
WES can provide insights into the genetic origins of Mendelian diseases or traits that are hard to study with conventional gene discovery strategies. Exome sequencing of parent–child trios is also a highly effective approach for identifying de novo coding mutations of a disease, as it is very unlikely that multiple de novo events occur in one specific gene.
1. Depending on your request, download the Custom Peptide Synthesis form or Modification Peptide Synthesis form.
2. Fill in the customer information fields
3. Upload the filled Peptide Synthesis form and Submit
4. Our colleagues will contact you
1. Depending on your request, download the Single Strand RNA Synthesis form or Double Strand RNA Synthesis form.
2. Fill in the customer information fields
3. Upload the filled Peptide Synthesis form and Submit
4. Our colleagues will contact you
1. Download the Gene Synthesis form and fill it with the necessary information. You can add more than one gene.
2. Fill in the customer information
3. Upload the filled Gene Synthesis form and Submit
4. Our colleagues will contact you as soon as possible
Our partnership with TWIST and Agilent allows us to offer you the best library kits for Whole Exome Sequencing. Here you can find our top selling library kits, their specifications and some useful information to prepare your sample
We advise sending samples in a volume ranging from 25 to 50 μl to prevent them from drying out during shipment
You can have a look to the list of all library kits available and the Macrogen Europe sample criteria. RTR samples? You can also find the library criteria in case your sample are ready for sequencing.
Now, if you like what you read or you have any extra questions, you can book a free online meeting to discuss your project with our consultants. Tell us about your project and we will get the correct consultant for you
You can have a look to the list of all library kits available and the Macrogen Europe sample criteria. RTR samples? You can also find the library criteria in case your sample are ready for sequencing.
Knowing the purpose of your research is essential to establish the correct sequencing configuration and statistic analysis. Let us know what is the objective of your research and we will guide you in getting the correct bioinformatics services.
For most researchers obtaining RAW data is sufficient for their research. However, Macrogen Europe is ready to provide bioinformatic analysis for your project.
Have a look at the top-selling standard and advanced bioinformatics reports for Whole Exome Sequencing.
The Advanced Bioinformatics services listed above are not available for custom target sequencing. Please, contact our team about extra BI services
Knowing the purpose of your research is essential to establish the correct sequencing configuration and statistic analysis. Let us know what is the objective of your research and we will guide you in getting the correct bioinformatics services.
