$79 / use

Healthcare Pro

Name: Healthcare Pro DNA Analysis App | Genetic Reports for Doctors
Brand: Sequencing.com
SKU: 4531
Price: 79.00 USD
Availability: Instock
Rating: 5 (10126 reviews)

App MD

Overview
Getting Started
Upload DNA Data
Order DNA Test Kits
Results
HIPAA, HITECH & BAAs
EMRs & Charts
FAQ
Price
Related Apps
Disclaimer

Genetic analysis and reports designed by physicians for healthcare providers.

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

This app analyzes your DNA and provides insights about health.

If your DNA data is not already stored in your Sequencing.com account, you can either import your data from a DNA test you've already taken or you can order a DNA test.

You've already taken a DNA test			You need a DNA test
Upload your DNA data			Order a DNA test

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

Use the Upload Center to upload and use your DNA test or genome sequencing data.

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 Whole Genome Sequencing test and Ultimate DNA Test.

Compare to 23andMe, Ancestry and similar that test less than 0.1% of your genome.

	Ultimate DNA Test	Whole Genome Sequencing
	BUY NOW	BUY NOW

Discounted Price	$69 ~~$189~~	$399 ~~$599~~

Amount of genome tested	1%	100%

Technology	Genotyping Microarray	Clinical-Grade 30x Genome Sequencing

Also Includes	Silver Membership to Sequencing.com	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.

In addition to the genetic report, the Healthcare Pro app results also include detailed information about the specific genes and genetic variants analyzed as well as the medical references that link the variant to a specific disease, medication reaction or trait. This information is easy to browse and search with some content linking out to additional information.

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

HIPAA Business Associate Agreement (BAA) are available.

Request a BAA

Learn more about our HIPAA and HITECH compliance.

The results have been specially designed to make them easy to:

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.

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

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.

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

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.