Add analysis services to the table

[beaugunderson]

First step is to figure out which services are offered for each provider. We should look at each product as well, in case the analysis services also differ by product.

• [ ] Nebula Genomics
• [x] Dante Labs
• [ ] Veritas Genetics
• [x] Full Genomes Corporation
• [ ] Genomics Personalized Health
• [ ] Gene by Gene
• [ ] YSEQ

We can add each service and their associated products to a comment here, and then see if there are common ideas that could become checkboxes for each product (though they may all vary enough that a short description would be better)

[beaugunderson]

Dante Labs

From their website:

• a "personalized report"
• a "Customized Report on a disease or a gene panel"
• "You will receive: Health Condition Report, Wellness and Longevity Report, Reaction to Medication Report and a Customized Report."
• "Customized reports on your selected diseases and conditions of interest are generated by the Dante Labs bioinformatics team. The Wellness & Longevity Report is generated in partnership with Sequencing.com."
• "What is the Secondary Report I receive together with the Customized Report? The Secondary Report includes variants and genes of diseases with similar symptoms to your chosen disease of interest. We have experienced that with complex diseases, up to 20% of patients have been misdiagnosed with the wrong disease. Therefore, this Secondary Report has proven to be a very useful tool for both patients and doctors to achieve a precise diagnosis, and prevent the ‘diagnostic odyssey’ experienced by rare disease patients."

[beaugunderson]

Full Genomes Corporation

• Whole genome: Basic analysis with ancestry reports: $75.00
  • "Our analysis of your whole genome data produces, variant summary reports, mtDNA sequence (as FASTA file), and Y-DNA analysis (for males)."
• Whole genome: Advanced Variant analysis: $250.00
  • "Our analysis of your whole genome data produces advanced and annotated variant summary reports suitable for advanced research."

Whole genome products include:

a. Y chromosome reports b. mitochondrial reports c. variant files (vcf) that are compatible with third party tools, such as Promethease d. raw data (BAM files)

The whole genome product is primarily for ancestry, but since health information is in the data, we recommend that the customer take the data either to a geneticist or genetic counselor or explore the data using third party tools. Note that FGC does not provide medical advice and we do not provide medical reports on the data ourselves. The goal of our product is to provide comprehensive ancestry results as well as make it possible for the customer to explore health results in consultation with appropriately qualified professionals if they desire to do so.