Name: Healthcare Pro DNA Analysis: Genetic Reports for Doctors
Brand: Sequencing.com
Price: 79.00 USD
Availability: Instock
Rating: 5 (5477 reviews)

<h2><img  src="https://uat.sequencing.com/sites/default/files/wysiwyg/14/healthcare-professional-dna-report.jpg" /></h2><h2><strong>Genetic analysis and reports designed by physicians for healthcare providers.</strong></h2><p>Universal compatibility enables this app to analyze genetic data from <em>any</em> laboratory or a genetic test provider.</p><p> </p><h2>A Genetic Report For Healthcare Professionals</h2><p>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.</p><p>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.</p><h3> </h3><p> </p><h2>Analyze Data From Any Test Including 23andMe, AncestryDNA, and MyHeritage</h2><p>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.</p><p>The Healthcare Pro app is the only DNA analysis app specifically designed to analyze the data from 23andMe, <a href="https://sequencing.com/blog/myheritage-review-dna-testing-and-geneology">MyHeritage</a> and similar tests and generate a report for healthcare providers. The report is written by doctors, for doctors and other healthcare professionals.</p><p>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.</p><div ><a href="https://sequencing.com/data/upload">Free DNA Data Upload</a></div><p> </p>


<h3><strong>This app analyzes a person's DNA and provides a health-focused genetic report designed for use by a healthcare professional.</strong></h3><p>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.</p><p>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.</p><table border="0" cellpadding="0" cellspacing="0" ><thead><tr><th ><h3><strong><span style="font-weight: 400;">You've already taken a DNA test</span></strong></h3></th><th ><h3><strong><span style="font-weight: 400;">You need a DNA test</span></strong></h3></th></tr></thead><tbody><tr><td style="text-align: center;"> </td><td> </td></tr><tr><td><img  data-fid="74870" data-media-element="1" src="https://sequencing.com/sites/default/files/wysiwyg/735/import_data_img_0.jpg" /></td><td><img  data-fid="74871" data-media-element="1" src="https://sequencing.com/sites/default/files/wysiwyg/735/2_kits_1.jpg" /></td></tr><tr><td style="vertical-align: middle; width: 539px; height: 55px;"><div style="margin: 0px;"><a href="https://sequencing.com/data/upload">Upload your DNA data</a></div></td><td style="vertical-align: middle; width: 539px; height: 55px;"><div style="margin: 0px;"><a href="https://sequencing.com/tests/order/genome-sequencing-dna-testing">Order a DNA test</a></div></td></tr><tr><td> </td><td> </td></tr><tr><td style="vertical-align: top;">Our Universal DNA Compatibility enables this app to work with DNA data from almost any genetic test including <a href="https://sequencing.com/blog/how-to-download-23andme-raw-dna-data" >23andMe</a>, <a href="https://sequencing.com/how-upload-raw-ancestry-dna-data-sequencingcom" >Ancestry</a>, <a href="https://sequencing.com/blog/myheritage-review-dna-testing-and-geneology" >MyHeritage</a>, <a href="https://sequencing.com/how-to-upload-raw-dna-data-genome-data-sequencing.com" >FTDNA</a>, and <a href="https://sequencing.com/what-is-whole-genome-sequencing-wgs" >genome sequencing</a>.</td><td style="vertical-align: top;">Our clinical-grade 30x Whole Genome Sequencing test obtains data on 100% of your genome.</td></tr></tbody>
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<h3><strong>Compatible with data from almost all DNA tests and genome sequencing services.</strong></h3><div ><a href="https://sequencing.com/data/upload">Free DNA Data Upload</a></div><p> </p><table align="left" border="0" cellpadding="0" cellspacing="5" ><thead><tr><th style="text-align: left;"><big>Test Compatibility</big></th><th style="text-align: left;"> </th><th style="text-align: left;"><big>Format Compatibility</big></th><th style="text-align: left;"> </th><th style="text-align: left;"><big>Variant Compatibility</big></th><th style="text-align: left;"> </th><th style="text-align: left;">Reference Genome Compatibility</th></tr></thead><tbody><tr><td><a href="https://sequencing.com/tests/order/genome-sequencing-dna-testing">Whole Genome Sequencing</a></td><td> </td><td>FASTQ and FQ</td><td> </td><td>SNP / SNV<br /><small>(Single Nucleotide Variants)</small></td><td> </td><td>hg38 / GRCh38</td></tr><tr><td>Exome Sequencing</td><td> </td><td>FASTA and FA</td><td> </td><td>INDEL<br /><small>(Insertion Deletion Variants)</small></td><td> </td><td>hg19 / GRCh37</td></tr><tr><td><a href="https://sequencing.com/tests/order/genome-sequencing-dna-testing">Ultimate DNA Test</a></td><td> </td><td>BAM</td><td> </td><td> </td><td> </td><td>hg18 / GRCh36</td></tr><tr><td>23andMe</td><td> </td><td>SAM</td><td> </td><td> </td><td> </td><td>hg17 / GRCh35</td></tr><tr><td>AncestryDNA</td><td> </td><td>CRAM</td><td> </td><td> </td><td> </td><td> </td></tr><tr><td>MyHeritage</td><td> </td><td>VCF</td><td> </td><td> </td><td> </td><td> </td></tr><tr><td>Dante Labs</td><td> </td><td>Genome VCF (gVCF and GVCF)</td><td> </td><td> </td><td> </td><td> </td></tr><tr><td>Nebula Genomics</td><td> </td><td>TXT</td><td> </td><td> </td><td> </td><td> </td></tr><tr><td>Genes for Good</td><td> </td><td>CSV</td><td> </td><td> </td><td> </td><td> </td></tr><tr><td>Living DNA</td><td> </td><td>TAB</td><td> </td><td> </td><td> </td><td> </td></tr><tr><td>HomeDNA</td><td> </td><td>gz and zip compressed files</td><td> </td><td> </td><td> </td><td> </td></tr><tr><td>FTDNA</td><td> </td><td>almost all other genetic data formats</td><td> </td><td> </td><td> </td><td> </td></tr><tr><td>Silverberry Genomix</td><td> </td><td> </td><td> </td><td> </td><td> </td><td> </td></tr><tr><td>Toolbox Genomics</td><td> </td><td> </td><td> </td><td> </td><td> </td><td> </td></tr><tr><td>Full Genomes</td><td> </td><td> </td><td> </td><td> </td><td> </td><td> </td></tr><tr><td>Color</td><td> </td><td> </td><td> </td><td> </td><td> </td><td> </td></tr><tr><td>New Amsterdam Genomics</td><td> </td><td> </td><td> </td><td> </td><td> </td><td> </td></tr><tr><td>24Genetics</td><td> </td><td> </td><td> </td><td> </td><td> </td><td> </td></tr><tr><td>Vitagene</td><td> </td><td> </td><td> </td><td> </td><td> </td><td> </td></tr><tr><td>Helix</td><td> </td><td> </td><td> </td><td> </td><td> </td><td> </td></tr><tr><td>Genos</td><td> </td><td> </td><td> </td><td> </td><td> </td><td> </td></tr><tr><td>tellmeGen</td><td> </td><td> </td><td> </td><td> </td><td> </td><td> </td></tr><tr><td>GSA</td><td> </td><td> </td><td> </td><td> </td><td> </td><td> </td></tr><tr><td>Axiom</td><td> </td><td> </td><td> </td><td> </td><td> </td><td> </td></tr><tr><td>almost all other genetic tests</td></tr></tbody>
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<h3><strong>This DNA analysis app is optimized for Sequencing.com's Ultimate Genome Sequencing service.</strong></h3><table border="0" cellpadding="0" cellspacing="0" style="font-family: times;"><thead><tr><th > </th><th style="text-align: center;"><p><a href="https://sequencing.com/tests/order/genome-sequencing-dna-testing"><img  data-fid="74160" data-media-element="1" src="https://sequencing.com/sites/default/files/wysiwyg/14/ultimate-dna-test-kit.jpg" style="height: 209px; width: 400px;" /></a></p><p><big><strong>Ultimate DNA Test</strong></big></p></th><th style="text-align: center;"><p><a href="https://sequencing.com/tests/order/genome-sequencing-dna-testing"><img  data-fid="74156" data-media-element="1" src="https://sequencing.com/sites/default/files/wysiwyg/14/ultimate-genome-sequencing-kit.jpg" style="height: 209px; width: 400px;" /></a></p><p><big><strong>Ultimate Genome Sequencing</strong></big></p></th></tr></thead><tbody><tr><td style="vertical-align: top;"> </td><td style="vertical-align: middle; text-align: center; width: 590px; height: 55px;"><div ><a href="https://sequencing.com/tests/order/genome-sequencing-dna-testing">ORDER NOW</a></div></td><td style="vertical-align: middle; text-align: center; width: 590px; height: 55px;"><div ><a href="https://sequencing.com/tests/order/genome-sequencing-dna-testing">ORDER NOW</a></div></td></tr><tr><td style="vertical-align: top; text-align: center;"> </td><td style="vertical-align: top;"> </td><td style="vertical-align: top;"> </td></tr><tr><td style="vertical-align: top;"><strong>Discounted Price</strong></td><td style="vertical-align: top; text-align: center;"><strong>$69</strong>  <span style="color: rgb(105, 105, 105);"><s>$189</s></span></td><td style="vertical-align: top; text-align: center;"><strong>$399</strong>  <span style="color: rgb(105, 105, 105);"><s>$599</s></span></td></tr><tr><td style="vertical-align: top; text-align: center;"> </td><td style="vertical-align: top;"> </td><td style="vertical-align: top;"> </td></tr><tr><td style="vertical-align: top;"><strong>Amount of genome tested</strong></td><td style="vertical-align: top; text-align: center;">1%</td><td style="vertical-align: top; text-align: center;">100%</td></tr><tr><td style="vertical-align: top;"> </td><td style="vertical-align: top;"> </td><td style="vertical-align: top;"> </td></tr><tr><td style="vertical-align: top;"><strong>Technology</strong></td><td style="vertical-align: top; text-align: center;">Enhanced Genotyping Microarray</td><td style="vertical-align: top; text-align: center;">Clinical-Grade 30x Genome Sequencing</td></tr><tr><td style="vertical-align: top;"> </td><td style="vertical-align: top;"> </td><td style="vertical-align: top;"> </td></tr><tr><td style="vertical-align: top;"><p><strong>Bonuses</strong></p></td><td style="vertical-align: top; text-align: center;"><p>Silver Membership to Sequencing.com</p><p><small>(includes your choice of DNA analysis apps &amp; reports)</small></p></td><td style="vertical-align: top; text-align: center;"><p>Silver Membership to Sequencing.com</p><p><a href="https://sequencing.com/wellness-and-longevity">Wellness &amp; Longevity Health Analysis</a></p><p><a href="https://sequencing.com/healthcare-pro-genetic-report">Healthcare Pro Report</a></p><p><a href="https://sequencing.com/rare-disease-screen-dna-report">Rare Disease Screen Analysis</a></p></td></tr></tbody>
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<h3><strong>A sample Genetic Report is provided in the 'Overview' tab and another sample reports appears below.</strong></h3><p><iframe src="https://docs.google.com/gview?url=https://drive.google.com/file/d/1GgkTZZsGZ0f4uS1Bi6B66DE9D9o5A_ec/preview&embedded=true" ></iframe></p>


<h3>Do I need to do anything to the file containing my genetic data before it is analyzed by this app?</h3><p>Good news... the app does everything for you.</p><p>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.</p><p>23andMe data can be uploaded or imported directly from 23andMe (via the <a href="https://sequencing.com/data/upload">Upload Center</a>) 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.</p><p>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.</p><p> </p><h3>Where do I specify sex and reference genome?</h3><p>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).</p><p> </p><h3>What do the question marks and dashes represent in the 'My Genetic Makeup' column of this table?</h3><div><div><big><strong>??</strong></big></div><div>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.</div><div style="margin-left: 40px;"> </div>
</div><div><div><big><strong>?</strong></big></div><div>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. </div><div> </div><div>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.</div><div style="margin-left: 40px;"> </div>
</div><div><div><big><strong>--</strong></big></div><div>Two dashes are used if your genetic data file <em>does</em> 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.</div><div> </div><div>Two dashes are used instead of question marks because the genetic data file <em>does</em> contain data on that variant but the variant's results are not reliable.</div><div style="margin-left: 40px;"> </div>
</div><div><div><big><strong>-</strong></big></div><div>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.</div>
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<p>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. </p><div ><a href="https://sequencing.com/apps/app-market">View All DNA Reports</a></div><p> </p><h3><strong>Additional Apps by App MD</strong></h3><h2><a href="https://sequencing.com/wellness-and-longevity"><img  style="height: 150px; width: 150px;" src="https://uat.sequencing.com/sites/default/files/wellness-and-longevity-app-icon-sequencingcom.png" /></a></h2><h4><a href="https://sequencing.com/wellness-and-longevity">Wellness &amp; Longevity</a></h4><p>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.</p><p> </p><p><a href="https://sequencing.com/rare-disease-screen-dna-report"><img  style="height: 150px; width: 150px;" src="https://uat.sequencing.com/sites/default/files/rare-disease-screen-app-sequencingcom.png" /></a></p><h4><a href="https://sequencing.com/rare-disease-screen-dna-report">Rare Disease Screen</a></h4><p>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).</p><p>View the <a href="https://sequencing.com/carrier-screening-rare-diseases-syndromes-and-traits" >full list of rare diseases, conditions, and traits</a> included in the Rare Disease Screen app.</p>


<p>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.</p>


Healthcare Pro

For professional use only. This app analyzes DNA data from any genetic test and provides a genetic health report designed for healthcare providers. Easy to use.

Healthcare Pro

Genetic analysis and reports designed by physicians for healthcare providers.

A Genetic Report For Healthcare Professionals

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

Sample Report