Sequencing Newsletter - September 2023
Sequencing.com
education at dna.sequencing.com
Wed Sep 27 21:14:11 BST 2023
Catch up on the month of September at Sequencing
https://links.dna.sequencing.com/z/n0xfn0qut?uid=b5dd70e0-a350-4d06-ac9b-9ae02ff7deb8&txnid=98d57de6-35c1-421f-8ac4-3ded8e01c1ff&mid=709bc508-3266-403d-9226-0645a3407d03&bsft_ek=2023-09-27T19%3A20%3A33Z&bsft_mime_type=text&bsft_tv=27&bsft_lx=1
September 2023
https://links.dna.sequencing.com/z/n0xfn0qut?uid=b5dd70e0-a350-4d06-ac9b-9ae02ff7deb8&txnid=98d57de6-35c1-421f-8ac4-3ded8e01c1ff&mid=709bc508-3266-403d-9226-0645a3407d03&bsft_ek=2023-09-27T19%3A20%3A33Z&bsft_mime_type=text&bsft_tv=27&bsft_lx=2
Current Sale - End Of Summer
Currently we are offering an End Of Summer Sale. Save Over 50% on our Disease Screen Bundle.
Valued at $1059 For only $419
Bundle Includes:
- Whole Genome Sequencing
- Next-Gen Disease Screenhttps://links.dna.sequencing.com/z/w7du939vk?uid=b5dd70e0-a350-4d06-ac9b-9ae02ff7deb8&txnid=98d57de6-35c1-421f-8ac4-3ded8e01c1ff&mid=709bc508-3266-403d-9226-0645a3407d03&bsft_ek=2023-09-27T19%3A20%3A33Z&bsft_mime_type=text&bsft_tv=27&bsft_lx=3
- Wellness and Longevity Reporthttps://links.dna.sequencing.com/z/2ildx45yi?uid=b5dd70e0-a350-4d06-ac9b-9ae02ff7deb8&txnid=98d57de6-35c1-421f-8ac4-3ded8e01c1ff&mid=709bc508-3266-403d-9226-0645a3407d03&bsft_ek=2023-09-27T19%3A20%3A33Z&bsft_mime_type=text&bsft_tv=27&bsft_lx=4
- Healthcare Pro Reporthttps://links.dna.sequencing.com/z/05bjgh6k1?uid=b5dd70e0-a350-4d06-ac9b-9ae02ff7deb8&txnid=98d57de6-35c1-421f-8ac4-3ded8e01c1ff&mid=709bc508-3266-403d-9226-0645a3407d03&bsft_ek=2023-09-27T19%3A20%3A33Z&bsft_mime_type=text&bsft_tv=27&bsft_lx=5
- Melanoma Skin Care Report
- Prevent Breast Cancer Report
[View End Of Summer Sale](https://links.dna.sequencing.com/z/n0xfn0qut?uid=b5dd70e0-a350-4d06-ac9b-9ae02ff7deb8&txnid=98d57de6-35c1-421f-8ac4-3ded8e01c1ff&mid=709bc508-3266-403d-9226-0645a3407d03&bsft_ek=2023-09-27T19%3A20%3A33Z&bsft_mime_type=text&bsft_tv=27&bsft_lx=6)
Reports of the Month
https://links.dna.sequencing.com/z/nshktyxp1?uid=b5dd70e0-a350-4d06-ac9b-9ae02ff7deb8&txnid=98d57de6-35c1-421f-8ac4-3ded8e01c1ff&mid=709bc508-3266-403d-9226-0645a3407d03&bsft_ek=2023-09-27T19%3A20%3A33Z&bsft_mime_type=text&bsft_tv=27&bsft_lx=7
Carrier Status: Provides insights into your genetic makeup, identifying potential risks for common and rare inherited conditions. [More Info](https://links.dna.sequencing.com/web-only/z/nshktyxp1?uid=b5dd70e0-a350-4d06-ac9b-9ae02ff7deb8&txnid=98d57de6-35c1-421f-8ac4-3ded8e01c1ff&mid=709bc508-3266-403d-9226-0645a3407d03&bsft_ek=2023-09-27T19%3A20%3A33Z&bsft_mime_type=text&bsft_tv=27&bsft_lx=8)
https://links.dna.sequencing.com/z/32kpxos67?uid=b5dd70e0-a350-4d06-ac9b-9ae02ff7deb8&txnid=98d57de6-35c1-421f-8ac4-3ded8e01c1ff&mid=709bc508-3266-403d-9226-0645a3407d03&bsft_ek=2023-09-27T19%3A20%3A33Z&bsft_mime_type=text&bsft_tv=27&bsft_lx=9
Disease Risk Genetic Test: A genetic report on your risk of cancers, heart disease, autoimmune diseases, Alzheimer's, and more. [More Info](https://links.dna.sequencing.com/web-only/z/32kpxos67?uid=b5dd70e0-a350-4d06-ac9b-9ae02ff7deb8&txnid=98d57de6-35c1-421f-8ac4-3ded8e01c1ff&mid=709bc508-3266-403d-9226-0645a3407d03&bsft_ek=2023-09-27T19%3A20%3A33Z&bsft_mime_type=text&bsft_tv=27&bsft_lx=10)
https://links.dna.sequencing.com/z/hrwmd006z?uid=b5dd70e0-a350-4d06-ac9b-9ae02ff7deb8&txnid=98d57de6-35c1-421f-8ac4-3ded8e01c1ff&mid=709bc508-3266-403d-9226-0645a3407d03&bsft_ek=2023-09-27T19%3A20%3A33Z&bsft_mime_type=text&bsft_tv=27&bsft_lx=11
Nourish: DNA-based nutrition plan offering insights into nutrient deficiencies, food sensitivities, and recommended diets. [More Info](https://links.dna.sequencing.com/web-only/z/hrwmd006z?uid=b5dd70e0-a350-4d06-ac9b-9ae02ff7deb8&txnid=98d57de6-35c1-421f-8ac4-3ded8e01c1ff&mid=709bc508-3266-403d-9226-0645a3407d03&bsft_ek=2023-09-27T19%3A20%3A33Z&bsft_mime_type=text&bsft_tv=27&bsft_lx=12)
Commonly Asked Questions
At [Sequencing.com](https://links.dna.sequencing.com/z/e6skci738?uid=b5dd70e0-a350-4d06-ac9b-9ae02ff7deb8&txnid=98d57de6-35c1-421f-8ac4-3ded8e01c1ff&mid=709bc508-3266-403d-9226-0645a3407d03&bsft_ek=2023-09-27T19%3A20%3A33Z&bsft_mime_type=text&bsft_tv=27&bsft_lx=13), we’re dedicated to helping you unlock the mysteries of your DNA. Here are some frequently asked questions to guide you on your genetic journey:
[What can I expect from Whole Genome Sequencing?](https://links.dna.sequencing.com/z/32m4v3hkq?uid=b5dd70e0-a350-4d06-ac9b-9ae02ff7deb8&txnid=98d57de6-35c1-421f-8ac4-3ded8e01c1ff&mid=709bc508-3266-403d-9226-0645a3407d03&bsft_ek=2023-09-27T19%3A20%3A33Z&bsft_mime_type=text&bsft_tv=27&bsft_lx=14)
Whole genome sequencing provides a complete blueprint of your DNA. With over 3 billion genetic variants identified, even genes whose purpose are not yet known will be included. This ensures that your sequencing results remain relevant and applicable to the latest genetic findings for years to come. After purchasing a sequencing service from us, you’ll receive a collection kit to start the process.
[How do genetics play a role in Multifactorial Disorders?](https://links.dna.sequencing.com/z/qvtec6oei?uid=b5dd70e0-a350-4d06-ac9b-9ae02ff7deb8&txnid=98d57de6-35c1-421f-8ac4-3ded8e01c1ff&mid=709bc508-3266-403d-9226-0645a3407d03&bsft_ek=2023-09-27T19%3A20%3A33Z&bsft_mime_type=text&bsft_tv=27&bsft_lx=15)
Diseases can develop through various mechanisms. While some are purely genetic, others arise from a combination of factors. Understanding the difference between single gene diseases and multifactorial disorders is crucial. Genomics offers insights into your past, present, and future health, enabling you to adopt strategies to prevent or manage diseases.
[What are the benefits of Genome Explorer Premium?](https://links.dna.sequencing.com/z/fcgw2ypbr?uid=b5dd70e0-a350-4d06-ac9b-9ae02ff7deb8&txnid=98d57de6-35c1-421f-8ac4-3ded8e01c1ff&mid=709bc508-3266-403d-9226-0645a3407d03&bsft_ek=2023-09-27T19%3A20%3A33Z&bsft_mime_type=text&bsft_tv=27&bsft_lx=16)
Genome Explorer Premium is the pinnacle of DNA exploration. Think of it as a Google for your DNA. It’s designed for users of all genetics knowledge levels, allowing you to delve deep into your DNA and learn about genetic conditions of interest. With features like Risk Version and Your Status, it’s never been easier to unlock the secrets of your DNA.
For more detailed answers and additional insights, please visit our [Education Center](https://links.dna.sequencing.com/z/ui8302xca?uid=b5dd70e0-a350-4d06-ac9b-9ae02ff7deb8&txnid=98d57de6-35c1-421f-8ac4-3ded8e01c1ff&mid=709bc508-3266-403d-9226-0645a3407d03&bsft_ek=2023-09-27T19%3A20%3A33Z&bsft_mime_type=text&bsft_tv=27&bsft_lx=17).
[Get Sequenced Here](https://links.dna.sequencing.com/z/e6qjf49ac?uid=b5dd70e0-a350-4d06-ac9b-9ae02ff7deb8&txnid=98d57de6-35c1-421f-8ac4-3ded8e01c1ff&mid=709bc508-3266-403d-9226-0645a3407d03&bsft_ek=2023-09-27T19%3A20%3A33Z&bsft_mime_type=text&bsft_tv=27&bsft_lx=18)
This Month In Genetics
https://links.dna.sequencing.com/z/fdk2yozb0?uid=b5dd70e0-a350-4d06-ac9b-9ae02ff7deb8&txnid=98d57de6-35c1-421f-8ac4-3ded8e01c1ff&mid=709bc508-3266-403d-9226-0645a3407d03&bsft_ek=2023-09-27T19%3A20%3A33Z&bsft_mime_type=text&bsft_tv=27&bsft_lx=19
Whole Genome Sequencing: A Revolution in Newborn Screening in North Carolina
Traditionally, newborns in North Carolina undergo screening for around 60 inherited conditions. However, with about 1 in 15 children being born with a rare disease, there's an evident gap in these standard tests.
The Early Check program, a joint effort by RTI International and the University of North Carolina at Chapel Hill, is ushering in a new era of screening. By harnessing the capabilities of Whole Genome Sequencing, the program can effectively detect almost all known rare diseases in one comprehensive test.
Set to launch on September 28th, the initiative aims to sequence the genomes of 5,000 newborns over the next year. This approach not only increases the number of detectable conditions but also ensures early diagnosis. An early insight into potential health challenges enables timely interventions, offering children better health prospects from the outset and providing parents and healthcare professionals with invaluable knowledge about a child's genetic health.
[Learn More](https://links.dna.sequencing.com/z/fdk2yozb0?uid=b5dd70e0-a350-4d06-ac9b-9ae02ff7deb8&txnid=98d57de6-35c1-421f-8ac4-3ded8e01c1ff&mid=709bc508-3266-403d-9226-0645a3407d03&bsft_ek=2023-09-27T19%3A20%3A33Z&bsft_mime_type=text&bsft_tv=27&bsft_lx=20)
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