How does this test work?
We will send you a DNA test kit. Follow the instructions in the enclosed brochure, send us back the filled test tube (saliva) and register on the evaluation page using the individual codes in the brochure. Important: Without this registration, we cannot assign the result to you! You will then receive an email as soon as the laboratory has evaluated your test (usually after about four to six weeks) and you can view the results on the evaluation page.
Technology
SNP analyses (single nucleotide polymorphism) are used to determine alleles of a known polymorphism of a target sequence. These SNPs are individual nucleotide positions within the genome that vary naturally in the population. There are two alleles at each locus, which can be occupied by bases (adenine (A), guanine (G), cytosine (C) and thymine (T)) that define our genetic makeup.
We pay particular attention to those genetic markers whose DNA sequence has a known location in the chromosome and whose hereditary characteristics and resulting genetic causes are supported by current studies. We only test genetic markers that are based on scientific study results (replication studies) and that have a significant influence on human metabolism.
Whole Genome Sequencing (WGS)
Although we only incorporate genetic markers that are backed by strong scientific evidence into our analyses, we test the entire genome using next-generation sequencing (NGS). This process is also known as low-pass whole genome sequencing (lpWGS), which is currently the most up-to-date and accurate technology for analysing the entire genome. Instead of analysing the genome multiple times, this latest technology allows us to optimise the sequence depth. The lpWGS technology used has already proven to be superior to conventional DNA microarray technology in terms of data volume, statistical accuracy and improved ability to detect genetic variants.
Regardless of the technology used, the raw data must be further interpreted in order to convey the results to the end user in a comprehensible manner. The interpretations are based on our proprietary algorithm and software, which analyse the raw data based on the current state of research.
The analyses are carried out in accordance with the highest quality standards. We use study results with high statistical reliability. These studies are characterised by a large test group of at least 1,000 participants and their independence. The quality of the tests is guaranteed by our experts from the fields of biotechnology, genetics, pharmacy, biochemistry, medicine, nutritional science and information technology.
Sample report
You can download a sample report as a PDF here: yourEPI_MyGenes360_Sample report
Instructions for saliva test
Here you will find detailed instructions on how to collect and send your saliva sample. Please remember to register your test kit before sending it, otherwise the results cannot be assigned to you.
Download as PDF: yourEPI_MyGenes360_Saliva_Test_new_2_tubes
Download as PDF: yourEPI_MyGenes360_Saliva_Test_old_1_tube
Register DNA test: https://mydna.yourepi.de/
Note: Null mutations cannot be detected by our test (e.g. GSTM1 null type). In this case, we recommend further diagnostics in a specialised laboratory (e.g. qPCR or MLPA).
