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.
Understanding next-generation-sequencing can be challenging. Knowing how much data your project needs is essential. Read and learn with Macrogen Europe.
Do you need to sequence the complete genomic information of your samples? 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).
Create an account on our ordering platform and submit orders right from your lab chair.
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.
Understanding next-generation-sequencing can be challenging. Knowing how much data your project needs is essential. Read and learn with Macrogen Europe.
WGS analyses an organism’s entire genome, as opposed to whole exome sequencing and targeted sequencing, which studies specific areas. For this reason, WGS is the sequencing option of choice to study factors that affect the entire genome and to analyze noncoding DNA.
WGS is essential in a wide range of scientific fields, both fundamental and applied. It can identify genetic variations across the genome, which is why it is commonly used in agriculture and evolutionary biology and in clinical and pharmaceutical applications such as infectious diseases, immunology, cancer research, various inherited conditions and drug development.
De novo sequencing offers a way to uncover genome information about microorganisms, animals and plants when no reference genome is available. The analysis works by assembling long parallel phases of genetic material without referencing an existing nucleotide sequence. This type of WGS is highly accurate and can replicate or complete a blueprint for complex or polyploid genomes.
Resequencing a genome involves comparing newly sequenced DNA to a previously created reference genome. It is a highly efficient, fast and cost-effective way of analyzing the genomes of commonly studied organisms. Whole genome resequencing can scan or test for specific genetic variations. Any differences between the sample DNA and the reference could be an indication of a new variant or a potential disorder in a clinical setting.
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.
Understanding next-generation-sequencing can be challenging. Knowing how much data your project needs is essential. Read and learn with Macrogen Europe.
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.
We have a partnership with different suppliers, such as Illumina and PacBio, that allows us to have a huge variety of library preparation kits for you. Have a look at our top-selling kits and the requirements to submit your samples.
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.
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
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 researches 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 Genome Sequencing (Human).
It indicates the average number o reads that align to a specific reference, and the read counts and average insert size of the fragments.
To identify how many changes a single nucletide in the DNA sequence.
Have a closer look to the SNP and INDEL information.
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.