Healthcare professional genetic health report

Genetic analysis and reports designed by physicians for healthcare providers.

Universal compatibility enables this app to analyze genetic data from any laboratory or a genetic test provider.

 

A Genetic Report For Healthcare Professionals

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.

 

Analyze Data From Any Test Including 23andMe, AncestryDNA, and MyHeritage

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.

 

Analysis Optimized for Whole Genome Sequencing data

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 DNA Collection Kit

Ultimate Genome Sequencing

 
   
Discounted Price $399  $599
   
Amount of genome tested 100%
   
Technology Clinical-Grade 30x Genome Sequencing
   

Bonuses

Silver Membership to Sequencing.com

Wellness & Longevity Health Analysis

Healthcare Pro Report

Rare Disease Screen Analysis

 

HIPAA, HITECH & BAAs

We are HIPAA-compliant, HITECH-compliant, Privacy Shield-compliant and GDPR-compliant.

A HIPAA Business Associate Agreement (BAA) is available.

Request a BAA

Learn more about our HIPAA and HITECH compliance.

 

EMRs & Medical Charts

This app generates a genetic report that's designed to integrate into your practice.

  • download as a PDF and quickly import into all EMRs and EHRs.
  • print and add to a chart.
  • securely share with your patient and other healthcare professionals.

If you'd prefer additional EMR/EHR integration, please submit a Support Request to discuss a customized solution.

This app analyzes a person's DNA and provides a health-focused genetic report designed for use by a healthcare professional.

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

   
   
Our Universal DNA Compatibility enables this app to work with DNA data from almost any genetic test including 23andMeAncestryMyHeritageFTDNA, and genome sequencing. Our clinical-grade 30x Whole Genome Sequencing test obtains data on 100% of your genome.

Compatible with data from almost all DNA tests and genome sequencing services.

 

Test Compatibility   Format Compatibility   Variant Compatibility   Reference Genome Compatibility
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

 

 

This DNA analysis app is optimized for Sequencing.com's Ultimate Genome Sequencing service.

 

Ultimate DNA Test Kit

Ultimate DNA Test

Ultimate Genome Sequencing DNA Collection Kit

Ultimate Genome Sequencing

 
     
Discounted Price $69  $189 $399  $599
     
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

Wellness & Longevity Health Analysis

Healthcare Pro Report

Rare Disease Screen Analysis

A sample Genetic Report is provided in the 'Overview' tab and another sample reports appears below.

Do I need to do anything to the file containing my genetic data before it is analyzed by this app?

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.

 

Where do I specify sex and reference genome?

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).

 

What do the question marks and dashes represent in the 'My Genetic Makeup' column of this table?

??
Two question marks are used when your genetic data file did not contain any data on this specific genetic variant and therefore the data was not tested for and is 'Unknown'. Two question marks are used because each person's DNA contains two copies of that genetic variant so there is one question mark for each copy of the genetic variant in your DNA.
 
?
A single question mark will appear when your genetic data file did not contain any data on this specific genetic and DNA commonly only contains a single copy of that genetic variant. 
 
For example, all variants on the mitochondrial chromosome (Chromosome "M") exist as a single copy because DNA only contains a single copy of the mitochondrial chromosome. This is different from most chromosomes, which appear duplicate (there are two copies of chromosome 1, two copies of chromosome 2, etc.). If the variant is on a chromosome that there is only a single copy of and there is no data on that variant in the data file then only a single question mark will appear.
 
--
Two dashes are used if your genetic data file does include information about this specific genetic variant but the data is a 'No Call.' A 'No Call' means the lab that generated the file determined that the variant's test result did not pass quality control. A 'No Call' may also appear when Sequencing.com's additional quality control determines a variant's result is not reliable and may provide inaccurate results. Sequencing.com has implemented this additional quality control to ensure that only the highest quality genetic data is analyzed by apps.
 
Two dashes are used instead of question marks because the genetic data file does contain data on that variant but the variant's results are not reliable.
 
-
A single dash is used when the variant's results are not reliable (ie the test result for that variant fails quality control) and DNA contains only a single copy of that variant. For example, all variants on the mitochondrial chromosome that are tested for by a genetic test but don't pass quality control have a single dash as the variant's result.

$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. 

 

Additional Apps by App MD

Icon for the Wellness and Longevity DNA Analysis App that provides easy to understand genetic interpretation of genome data with a focus on identifying genetic disease risk and personalized preventions using the DNA tests from 23andMe, Ancestry & FTDNA.

Wellness & Longevity

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 to personalized health optimization.

 

Icon for the Rare Disease Screen DNA Analysis App that provides genetic interpretation for more than 1,000 orphan and rare diseases, syndromes and traits using genome and DNA test data from 23andMe, AncestryDNA, Helix, MyHeritage and FamilyTreeDNA.

Rare Disease Screen

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.