Analyze patient DNA with ease — detect infections, search for cancer markers and explore the microbiome. This tool will take a DNA file and analyze the DNA data that was not used to assemble the regular chromosomes. That may include non-human DNA or human DNA with large mutations. The result of the DNA search will be a report of viral, bacterial and fungal sequences present. The second search in this tool will look for possibly carcinogenic mutations.
Please log in to use. If you do not have an account, please register.Whole Genome Sequencing (WGS) captures all DNA fragments (“reads”) present in a biological sample. If this sample is human, most of these reads will be human and used to assemble the chromosomes. If a whole genome sequence is available, it is possible to extract more medical information than just the chromosomes.
Usually, bacterial, viral, or fungal DNA is present too, but this data is not often used clinically. These unused reads can offer valuable diagnostic insights, also depending on where the sample came from:
- Intestinal or oral samples may reveal microbiome imbalances (i.e. which bacteria were present?)
- Blood samples may uncover circulating pathogens (i.e. viruses)
Additionally, blood can contain cell-free DNA (cfDNA), released by dying (f.e. cancer) cells. Analyzing cfDNA may therefore help search for cancer-associated mutations and better understand disease progression.
If you have a .bam (or .fastQ) file, you can upload it in this tool straight-away. If you do not, you can order a sequence at Dante Labs. They will provide a .bam file. Please note that there are cost associated with the test and it takes at least a few weeks for the results to be available.
Account Required — Why We Charge a Small Fee
Running advanced DNA analysis requires powerful servers and secure infrastructure to process large files and protect sensitive data. Unfortunately, this comes with significant ongoing costs.
To keep the service reliable, fast, and secure, we ask users to create an account and contribute a small fee per month. This helps us:
- Maintain high-performance servers
- Ensure privacy and data security
- Continue improving the analysis tools
We aim to keep pricing as low as possible — just enough to cover operational expenses.
Thank you for your understanding and support.
Privacy First — Your Data Is Never Stored
We take patient privacy and data protection very seriously.
When you upload a DNA file (e.g. BAM or FASTQ), it is used only for analysis.
As soon as the analysis is complete, the file is automatically and permanently deleted from our servers.
We do not:
- Store or archive any individual DNA data
- Use uploaded files for AI training, research, or any secondary purpose
Our system is designed to handle data transiently, ensuring full confidentiality.
Please log in to use. If you do not have an account, please register.