Decode the 100% from your genome
Whole Genome Sequencing (WGS)
&
Whole Exome Sequencing (WES)
With WGS and WES, we offer you the first kit on the market consumption of full sequencing.
You will receive the kit at your home, you only need one saliva sample.
Afterwards, our laboratory will extract the DNA and sequence your entire genome.
Get your genetic results with high coverage and quality.
You will have it all with WGS and WES
Your genome available for life
Explore your genome
Download VCF (Variant Call Format) files for the analysis of your genetic variants, as well as BAM and FASTQ files, so that you have all your genetic data.
ADNTRO REPORTS
Access all ADNTRO reports with the maximum precision by using all of your DNA to determine genetic associations from GWAS studies
Ready for diagnostics
Our exome or whole genome sequencing data is of the highest quality and can be used by doctors and genetic counselors.
GENETIC CONSULTATION
We offer the possibility (with additional cost) to receive consultation and advice from our genetic and bioinformatics team to help you with all your questions about your results.
Choose genomic technology
From ADNTRO we offer you different options to explore all your DNA through your genetic diagnosis and we accompany you during the process
399€
LOW PASS (4x)
- 100% of your sequenced DNA
- 23,000 genes
- Access to ADNTRO reports +1 year of updates
- Quality report
- File delivery
- Not valid for diagnosis (4x average coverage)
950€
High Pass (30x)
- 100% of your sequenced DNA
- 23,000 genes
- Access to ADNTRO reports + 1 year of updates
- Quality report
- Detailed file delivery
- Ready for diagnostics (30x average coverage)
On Request
EXOME (150x)
- 100% from your sequenced exome
- 23,000 Genes - All variants of your genes
- Possibility of studying virtual gene windows (virtual gene panels)
- Detailed file delivery
- Quality report
- Ready for diagnostics (150x average coverage)
What we give you
You will receive a report about the reading of your genome with quality parameters.
Access to the ADNTRO online platform, with access to all the reports calculated from your genome.
A DNA Circos Plot generated from your DNA like the one shown below
Possibility of hiring a clinical analysis or diagnosis based on your data. (Not included in the initial price)
WGS, WES and Genotyping Differences
Frequent questions
Genotyping analyzes those variants of our genome that are polymorphic, that is, they show great variability between people and are very common in general (> 1% in the population). Genetic association studies (GWAS) are fundamentally based on this type of analysis and help to determine our predisposition to different diseases as well as to determine phenotypic variations in individuals.
Genotyping techniques analyze approximately 700,000 positions in our DNA; compared, whole genome analysis (WGS), in which all your DNA is analyzed (the three billion base pairs) and therefore allows the detection of rare variants in the population; These rare variants tend to have a high impact on the development of diseases, susceptibilities to diseases and on the response to treatments and it is the most used technique in genetic research in the world.
Surely you have seen our Home Kit, our genetic tests with a cheaper price.
With these microarray kits we perform genotyping, with which approximately 700,000 positions of your DNA are read, which is sufficient for some common traits but cannot be used for diagnosis or detection of rare variants.
With the complete sequencing of the genome (Whole Genome Sequencing) we can analyze its complete DNA (3,200,000,000 positions).
Our own comparative studies between 4x and 30x show a quality level of 90% + with differences in those regions and variants that are more difficult to detect that can only be determined with 30x
The difference lies in the level of your DNA coverage - 4x coverage means that each position of your DNA letter sequence has been read an average of 4 times. To be able to make a clinical diagnosis, a greater coverage is necessary to determine your genetic variants, of at least 30x. That is, each DNA position is read at least 30 times on average.
Our own comparative studies between 4x and 30x show a quality level of 90% + with differences in those regions and variants that are more difficult to detect that can only be determined with 30x
From ADNTRO we send you a kit to your home to collect the DNA sample (a simple saliva sample, 2ml) - The delivery to your home, as well as the return of the sample to the laboratory, is included in the price.
From your arrival at the laboratory (approx. 5 business days in Europe), your results will be ready in 4 weeks.
You can access your results online, explore all sections of ADNTRO (including health and pharmacogenetics) and download files with your genetic information.
The possibility of a genetic consultation with a professional team certified by the European Union in molecular genetics is offered; As well as by the DNATRO bioinformatics team. The consultation will be via email where you can solve your doubts regarding your results and we will help you in everything that is necessary.
No clinical diagnosis is offered, for which you should consult with your doctor
If you decide to carry out an exome or genome, we give you the possibility of carrying out targeted analysis of genes in which we will tell you the variants detected in a specific subset of genes. You can contact us by filling out this contact form for more details.
We will give you several formats so you can explore your DNA.
For the WGS High-Pass you will receive:
- FASTQ
- BAM and BAI
- VCF SNP
- VCF CNV
- VCF INDEL
- Others: XLS, PDF of reports, ...
- Bonus: Circus Plot
- Diagnostic report (contracted separately)
For the WGS Low-pass:
