Universal compatibility enables this app to analyze genetic data from any laboratory or a genetic test provider.
The Healthcare Pro app DNA analysis app provides a genetic report designed for healthcare professionals. The report analyzes a person's genetic risk for a wide range of diseases, health-relevant traits, and medication reactions.
The results also include detailed information about the specific genes and genetic variants analyzed as well as the medical references that link each genetic variant to a specific disease, medication reaction, or trait. This information is easy to search and browse. Content also links out to relevant ClinVar and pubmed articles.
Have you been asked by a patient to review data from an online direct-to-consumer genetic test such as 23andMe? While the actionability of the information provided by the test company may be lacking, the raw DNA data does contain a tremendous amount of useful information. The quality of these tests, known as genotyping DNA microarrays run in CLIA-certified CAP-accredited labs, is also usually very high.
The Healthcare Pro app is the only DNA analysis app specifically designed to analyze the data from 23andMe, MyHeritage and similar tests and generate a report for healthcare providers. The report is written by doctors, for doctors and other healthcare professionals.
Healthcare Pro is compatible with data from almost all DNA tests and genome sequencing services. This includes whole genome sequencing data, such as from our own Ultimate Genome Sequencing service or any other genome sequencing provider.
While Healthcare Pro can analyze raw DNA data from almost any genetic test, it is optimized for data from whole genome sequencing (WGS). This is because Healthcare Pro incldues a comprehensive screen of rare diseases and this screen works best with genome sequencing data.
When using Healthcare Pro, we recommend Sequencing.com's Ultimate Genome Sequencing service. If you're interested in providing this service, please request DNA collection kits for your practice.
All data, including the results of our Ultimate Genome Sequencing service, is protected by our Privacy First policy. Your patient owns their data. We never share or share the data, including DNA data, with anyone.
Ultimate Genome Sequencing |
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Discounted Price | $399 |
Amount of genome tested | 100% |
Technology | Clinical-Grade 30x Genome Sequencing |
Bonuses |
Silver Membership to Sequencing.com |
We are HIPAA-compliant, HITECH-compliant, Privacy Shield-compliant and GDPR-compliant.
A HIPAA Business Associate Agreement (BAA) is available.
Learn more about our HIPAA and HITECH compliance.
If you'd prefer additional EMR/EHR integration, please submit a Support Request to discuss a customized solution.
Once your DNA data is stored in your Sequencing.com account, purchase this DNA report, and then click the app's 'Start' button. You'll receive your report in about 30 minutes.
If your DNA data is not already stored in your account, you can either import your data from a DNA test you've already taken (such as from 23andMe or AncestryDNA) or you can order one of our DNA tests.
You've already taken a DNA test |
You need a DNA test |
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Our Universal DNA Compatibility enables this app to work with DNA data from almost any genetic test including 23andMe, Ancestry, MyHeritage, FTDNA, and genome sequencing. | Our clinical-grade 30x Whole Genome Sequencing test obtains data on 100% of your genome. |
Test Compatibility | Format Compatibility | Variant Compatibility | Reference Genome Compatibility | |||
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Whole Genome Sequencing | FASTQ and FQ | SNP / SNV (Single Nucleotide Variants) |
hg38 / GRCh38 | |||
Exome Sequencing | FASTA and FA | INDEL (Insertion Deletion Variants) |
hg19 / GRCh37 | |||
Ultimate DNA Test | BAM | hg18 / GRCh36 | ||||
23andMe | SAM | hg17 / GRCh35 | ||||
AncestryDNA | CRAM | |||||
MyHeritage | VCF | |||||
Dante Labs | Genome VCF (gVCF and GVCF) | |||||
Nebula Genomics | TXT | |||||
Genes for Good | CSV | |||||
Living DNA | TAB | |||||
HomeDNA | gz and zip compressed files | |||||
FTDNA | almost all other genetic data formats | |||||
Silverberry Genomix | ||||||
Toolbox Genomics | ||||||
Full Genomes | ||||||
Color | ||||||
New Amsterdam Genomics | ||||||
24Genetics | ||||||
Vitagene | ||||||
Helix | ||||||
Genos | ||||||
tellmeGen | ||||||
GSA | ||||||
Axiom | ||||||
almost all other genetic tests |
Ultimate DNA Test |
Ultimate Genome Sequencing |
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Discounted Price | $69 |
$399 |
Amount of genome tested | 1% | 100% |
Technology | Enhanced Genotyping Microarray | Clinical-Grade 30x Genome Sequencing |
Bonuses |
Silver Membership to Sequencing.com (includes your choice of DNA analysis apps & reports) |
Silver Membership to Sequencing.com |
Good news... the app does everything for you.
All you need to do is either upload or import the file containing your genetic data into your Sequencing.com account. Start the app, select the file and the app will handle do everything else.
23andMe data can be uploaded or imported directly from 23andMe (via the Upload Center) while Ancestry.com, Family Tree DNA and The Genographic Project data can be obtained from those services and then uploaded to your account at Sequencing.com. You don't need to do anything to the file you obtain from these services... just upload the file to your secure account at Sequencing.com and then you can use it to power most apps.
Both whole and exome sequencing data can be provided unaligned (such as in FASTQ or FASTA formats), aligned but without variant calling (such as BAM or SAM formats) or in VCF, CRAM or AVRO formats.
Some more good news... the app does this as well. It utilizes an advanced automated approach to determine sex and reference genome (if the file format is downstream of alignment).
$79
Sequencing.com is the world's largest collection of DNA analysis apps and reports. We have an app for almost everything you can find out from your genes.
Clear solutions for better health. This app analyzes dozens of preventable diseases such as heart disease and cancer and empowers the layperson with a straightforward, actionable report focused on personalized health optimization.
Analyzes more than 1,200 rare diseases, syndromes conditions and traits. Determines whether a person is a carrier of, or likely affected by, one or more rare diseases. Useful for comprehensive analysis of genetic data as well as preconception screening (to identify diseases a person may carry and may pass on to their children).
View the full list of rare diseases, conditions, and traits included in the Rare Disease Screen app.
The genetic analysis and statements that appear in this app and report have not been evaluated by the United States Food and Drug Administration. The Sequencing.com website and all software applications (Apps) that use Sequencing.com's website, as well as Sequencing.com's open Application Programming Interface (API), are not intended to diagnose, monitor, treat, cure, prevent nor alleviate any disease.