Unlock the secrets of your genome with a comprehensive DNA test that tells about your genetic vulnerability to complex diseases, inherited diseases, pharmacological compatibility, personal traits, wellness and ancestry.
DNAlyse OÜ acts solely as a facilitator of advanced genetic analysis services provided by certified and compliant third-party laboratories. We specialize in serving medical professionals, researchers, and institutional clients in need of reliable, data-driven genetic insights.
We do not access, store, or process personal or genetic data. Our role is limited to enabling secure and efficient access to genetic testing services for informational and research-support purposes only.
Our services are not intended for clinical diagnosis or medical decision-making. Any health-related conclusions drawn from the data should always be interpreted by qualified healthcare professionals within a clinical context.
DNAlyse OÜ on Eestis registreeritud ettevõte, mis tegutseb üksnes geneetiliste analüüsiteenuste vahendajana. Teenuseid osutavad sertifitseeritud ja EL-i õigusaktidele vastavad kolmandatest osapooltest laborid. Meie fookus on suunatud teadlastele, tervishoiutöötajatele ning institutsionaalsetele partneritele, kes vajavad usaldusväärseid ja teaduspõhiseid geneetilisi andmeid.
DNAlyse ei töötle, kogu ega salvesta isikuandmeid ega geneetilist teavet. Meie roll on piiratud turvalise ja tõhusa ligipääsu võimaldamisega geneetilistele testimisteenustele.
Teenused on mõeldud üksnes informatiivseks ja teadusuuringuid toetavaks otstarbeks ning ei asenda kliinilist diagnoosi ega arsti konsultatsiooni. Kõiki tervisega seotud tulemusi tuleb tõlgendada koos vastava eriala spetsialistiga.
From saliva to insight — every step is engineered for accuracy, security and reproducibility at scale.
There are 46 chromosomes (22 pairs of autosomes and one pair of sex chromosomes) in every cell nucleus. The XY chromosome is linked to the male sex, whereas the XX chromosome is linked to the female sex. The mitochondria also contains DNA. There are about 22 000 genes in the human genome.
A genetic variant is when a section of the DNA deviates from the reference. Variations can impact larger sections of the genome — substitutions, insertions, deletions — or change a single base (a single nucleotide polymorphism, SNP).
Scientific research based on genome-wide association studies (GWAS) and whole genome sequencing (WGS) is being used for defining variants. Such studies compare the genetic sequences of affected with those of healthy humans to identify possible pathological variants.
Your DNA is extracted from your saliva sample with laboratory methodologies that guarantee highest possible quality. It is then attached to a genotyping chip (array). Hybridization & fluorescence techniques determine whether a genetic variant exists in different DNA positions.
Large numbers of variants with high precision and an error rate of less than 1% are analyzed by this methodology. This accuracy is supported by the use of customized Illumina's Global Screening Array (GSA) chip with more than 780 000 markers and Illumina HiScan, known to be one of the most powerful and accurate on the market.
The last step involves data analysis by an expert team of geneticists and bioinformaticians. Powerful algorithms and software guarantee, with current techniques, maximum accuracy and report reliability. In addition, your information is constantly updated and improved.
The entire process complies with the strictest security and privacy standards by one of the leading laboratories in Europe. In fact, it is the only laboratory in Europe being capable of processing the high number of samples that are received and processed on a monthly basis.
One sample. Six dimensions of insight. 440+ meaningful, clinically relevant features.
Complex diseases are caused by a combination of genetic factors, environmental factors and lifestyle. We analyse such genetic factors and provide a health report regarding your vulnerability to develop such conditions.
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We analyse genetic variants associated with inherited conditions. Some of these are pathologically recessive and occur only when having two variants being inherited by each parent. If only one variant is present, then such 'carriers' do not have the condition but can transfer it to their children. This health report also investigates pathologically dominant conditions.
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We analyse your response to certain drugs based on your genetic variants. Do NOT STOP taking any medication, neither change your dose without consulting your doctor.
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Physical and wellness-associated traits are caused by a combination of genetic factors, environmental factors and lifestyle. We analyse such genetic factors to provide trait and wellness report regarding your likelihood of developing different traits, as well as the presence or absence of key genetic variants that influence such development.
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Ethnic and Geographical Origins (53 ethnic groups). Paternal haplogroup. Maternal haplogroup. Percentage of Neanderthal DNA. How ancestry is distributed in different populations and ethnicities.
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Designed specifically for researchers, healthcare professionals, and institutional clients. All features are clinically relevant and based on validated scientific sources — no novelty reports or fluff.
Understand genetic predispositions through quantitative values (risk scores, carrier percentages). Results are easy to interpret, even for comparative studies.
We prioritize the most relevant markers — diabetes, cardiovascular risk, drug metabolism — rather than listing rare or recreational traits just to inflate numbers.
All results are grouped clearly. We don't artificially split features into separate categories just to sell "more."
Fast and reliable shipping of test kits, free of charge.
Continuous updates based on evolving research and genetic imputation methods. Your reports grow as science advances.
Already tested elsewhere? Upload your raw DNA file and get enhanced, focused interpretation — without redundant commentary.
Our pricing structure is tailored for research projects, medical practices, and bulk testing — making high-quality analysis accessible and scalable.
This test was a valuable addition to my research project — it delivered actionable insights with clear, quantifiable results. I will definitely use it again in future studies.— Dr. Daniel Palkovics, Semmelweis University, Hungary
One sample, six categories of insight, 440+ clinically meaningful features.