Diploid | Human Genome Interpretation For Commercial Labs
Commercial Labs

Diploid for clinical labs

Don’t just offer exome or whole genome sequencing. Leverage Diploid to offer your clients an end-to-end clinical diagnostic service.

Your lab currently provides whole exome and whole genome sequencing services to your clients. Wouldn’t it be great if you could offer them full diagnostics and precision medicine services? With Diploid, you can. Simply upload your client’s NGS data to our service, and we will convert BAM and/or VCF files into a medical report, signed by a board certified medical geneticist (MD). You can then return this report to your client, together with the raw sequencing data. Reports can be branded with your lab’s logo.

Why Diploid?

High-quality

High-Quality

Among the very best worldwide in the Genomics England contest

Patent pending software platform that learns from previously solved cases

Automatically scans the literature for new associations using text mining algorithms

Includes specific in silico predictions for variants located in splice site regions

Not limited to coding regions: leveraging ENCODE to include non-coding regions in our analyses

Includes secondary findings according to the ACMG guidelines (upon request)

Proprietary database of pathogenic and control mutations (> 16 million annotated variants)

Reports always signed by both an MD with specialisation in clinical genetics and by a PhD in molecular genetics

Reports delivered as PDF files with click-through links for references and external data sources (e.g. OMIM, dbSNP, ClinVar, etc)

Consistently solving more cases than the competition


Order today, receive
results before:

Fast

JUN

16

Fast

Standard turn around time of 14 business days - faster than any other company

Fast-track service going from data to report in 7 business days, unseen in our industry


Affordable

Affordable

Prices start at $550 USD (€490 EUR) for a single exome or whole genome

Significant volume discounts are available, contact us for a custom quote

Outsourcing genome interpretation to us costs about 50-65% less than doing it in-house


Secure

Secure

Data centre received ISO27001 certification and completed multiple SAS70 Type II audits

256-bit SSL encryption for all data both in storage and in transit

Fully HIPAA compliant


Personal

Personal

Reopening cases for free when new medical information becomes available

Geneticists and MDs are available to answer any questions

Guaranteed response within 1 business day


How it works

Diploid combines expertise in bioinformatics and software engineering with world-class experience in rare disease diagnostics. The result is a procedure that is partly automated, partly manual to ensure clinical reports of the highest quality.

When NGS data comes in:

Variant calling

Our proprietary genome analysis platform starts with variant calling (if needed)

Variant annotation

The second step is variant annotation, using hundreds of annotation sources, including our proprietary database of pathogenic and control mutations (> 16 million annotated variants)

Phenotypic data

After quality checks, our geneticist enter phenotypic data for this case and our platform automatically compiles a list of genes that have been associated with any of the symptoms.

Filtering variants

Our geneticists then filter the list of variants based on our rich annotation. Out of tens of thousands of variants, they retain about 1-3 variants that are most likely to cause the phenotype in the patient.

Write report

They write a custom discussion for every candidate variant, explaining how the variant could contribute to the symptoms.

Signed report

The report is signed by a board-certified medical geneticist (MD) and returned as a PDF file.

Download Report

Try it for free

You don't have to take our word for it: we offer hospitals, commercial labs or researchers a free first interpretation of a clinical sample. See for yourself why leading research institutes and genetics labs are outsourcing their genome interpretations to us.

Try now