![]() Users can search Promethease reports by gene names You can also search for keywords like eyes or cancer. For example, you can search for variants in the MTHFRgene or BRCA1 gene, the latter of which is closely associated with breast cancer. Users can also search by keywords for specific genes, body parts, or conditions. This is especially useful because many other DNA analysis services provide reports without explaining how they were produced. Users can also filter by the number of academic references and the strength of the evidence. For example, users can search for specific medical conditions like AIDS or prostate cancer. Sample Promethease report identifying an increased risk of Alzheimer’s disease Upon opening their results, users find a list of gene variants from their uploaded DNA file that Promethease analyzed. Sections of these can also be downloaded to PDFs or exported to Excel spreadsheets. The report results are made available through a web browser. Promethease offers sample reports for customers to review before uploading their data and making an order. The company generates the report, and you will receive a link to it in an email. ![]() Then purchase the genetic report, and enter your contact information. Simply upload your raw DNA data (e.g., files from 23andMe, AncestryDNA, VCF, etc.). Getting started takes just a few minutes, depending on the file size. “I accept the risk of learning that I may be at high risk for a debilitating disease”Īnd “I am aware that I am strongly encouraged to discuss my Promethease report with a doctor”Īfter accepting the terms, users are asked to watch a tutorial video from 2016. The website first greets users with its terms and conditions. Review of Getting Started with Prometheaseīefore we review Promethease reporting, let’s take a look at how to get started using the service. This information can also be run through Promethease for additional analysis. Nebula offers variant interpretation tools, deep ancestry, and new reports every week. Nebula Genomics offers Whole Genome Sequencing, providing 10,000 times more information than most genotyping based genomics tests. Want the most comprehensive sequencing to run through Promethease? The first upload costs $12, but simultaneous additional files only cost only $4. ![]() However, you can upload multiple DNA raw data files at once for a reduced cost. Users can go from their results to the scientific studies behind those results with just a few clicks.Įach Promethease DNA report costs $12 and is generated in under 15 minutes.ĭoes Promethease offer discounts? Not usually. The company is very transparent about the sources of its data. Each item carries a brief description, details about biology, and an assessment of the medical significance. The Promethease service can be used to analyze medical history and genetic health risks based on family history. The health report is presented as a list of relationships between users’ gene variants and health traits. This report is based on genetic data from academic research aggregated on – a database of single nucleotide polymorphisms (SNPs). Its flagship product is a DNA health report. The Promethease test is compatible with raw data exports from Nebula Genomics, 23andMe, AncestryDNA, etc. It is designed to be compatible with raw data from other genetic testing providers. It does not offer any DNA ancestry or family tree maker services. Instead, this company focuses on analyzing genetic markers in uploaded raw DNA data and providing detailed health reports. Promethease is a DNA data analysis and literature retrieval system that does not offer DNA testing services. ![]() Read more in our Promethease review! Looking for DNA data to upload to sites like Promethease? Nebula Genomics offers Whole Genome Sequencing that decodes 100% of your DNA! This enables comprehensive and accurate reporting for health and ancestry and one of the best DNA tests for Promethease. Each entry in the SNPedia library is selected based on actual genetic information and results from peer-reviewed scientific research. The SNPedia library contains health information on over 100,000 gene variants. The company uses SNPedia’s extensive research library to inform users of their genetic variants. Promethease and SNPedia have become some of the most widely used sites for DNA health reporting. The genealogy platform MyHeritage acquired both websites in 2019. The site launched in 2008 and is based on the SNPedia wiki. Promethease is a website used for genome health reporting.
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