Interested in becoming a sponsor of DNA Today? Sponsors have featured interviews and advertisements on the podcast, promotion on social media (including giveaways), spotlights on this page, website banners, newsletter feature (to over 6,600 people) and more! Email Kira Dineen at info@DNAtoday.com for our full media kit, next steps, and more. We have 60 sponsors and counting!
Sarepta is a global biotechnology company on an urgent mission: engineer precision genetic medicine to reclaim futures otherwise impacted by rare diseases. They are in a daily race to transform genetic understanding into genetic medicines. Their multi-platform Precision Genetic Medicine Engine includes gene therapy, RNA and gene editing approaches. Sarepta is collaborating with health networks and payers, rethinking pricing models for revolutionary new treatments in development. Learn more about Sarepta on their website.
What is the most common inherited muscular dystrophy that primarily affects males? That would be Duchenne muscular dystrophy, or DMD for short. It affects mostly people assigned male at birth because it’s an X-linked condition1. Approximately 1 in 3,500 to 5,000 males born worldwide have the condition (2,3). How does DMD affect the muscles? Over time muscles become weak, particularly in the legs. Usually this becomes noticeable between the ages of 3 and 5 years old1. Unfortunately, as kids get older their heart and breathing muscles weaken and this becomes life threatening (4). Genetic testing is a critical step in diagnosing any genetic disease. Knowing the specific mutation can affect decisions on which therapeutic approaches might be appropriate for disease management (5). Cost should never be a barrier to genetic testing: genetic testing is often covered by insurance and in the US there are several sponsored no-charge testing options for people with suspected muscular dystrophies, including Invitae Detect MD and Perkin Elmer Decode Duchenne. You can also learn more at duchenne.com.
1. Aartsma-Rus A, Ginjaar lB, Bushby K. The importance of genetic diagnosis for Duchenne muscular dystrophy. J Med Genet. 2016;53:145-151.
2. Emery AEH. Population frequencies of inherited neuromuscular diseases--a world survey. Neuromuscul Disord. 1991;1:19-29.
3. Crisafulli S, Sultana J, Fontana A, et al. Global epidemiology of Duchenne muscular dystrophy: an updated systematic review and meta-analysis. Orphanet J. Rare Dis. 2020;15:141-161.
4. Emery AEH. The muscular dystrophies. Lancet. 2002;359:687-695
5. Birnkrant DJ, Bushby K, Bann CM, et al; for the DMD Care Considerations Working Group. Diagnosis and management of Duchenne muscular dystrophy, part 1: diagnosis, and neuromuscular, rehabilitation, endocrine, and gastrointestinal and nutritional management. Lancet Neurol. 2018;17:251-267.
Which muscular dystrophy causes weakness of the muscles typically starting around the hips and shoulders? That would be limb girdle muscular dystrophy, or LGMD. LGMD is a group of neuromuscular diseases caused by mutations in genes responsible for proteins critical for muscle function, regulation, and repair (1-3). It’s important for people clinically diagnosed or suspected of having LGMD to receive genetic testing to confirm the diagnosis. Why? There are so many reasons, including disease specific management, potential eligibility to be a participant in clinical trials, and knowing the risk to other family members (4). Cost should never be a barrier to genetic testing: genetic testing is often covered by insurance and in the US there are several sponsored no-charge testing options for people with suspected muscular dystrophies, including Invitae Detect MD, Perkin Elmer Decode Duchenne, and Perkin Elmer Lantern Project. Links in the show notes and on dnatoday.com. You can also learn more at limbgirdle.com.
1. Murphy AP and Straub V. J Neuromusc Dis. 2015;2(suppl. 2):S7-S19.
2. Liewluck T and Milone M. Muscle Nerve. 2018;58(2):167-77.
3. McNally EM. The Sarcoglycans. In: Landes Bioscience. 2000–2013.
4. Narayanaswami et al. Evidence-based guideline summary: Diagnosis and treatment of limb-girdle and distal dystrophies. American Academy of Neurology. 2014: 1453-1463.
Are you interested in the rapidly growing field of genetics and want to learn more about clinical genetics, molecular genetics, and laboratory science? Then you should check out the Genetic Assistant Online Training Program at Johns Hopkins University School of Medicine! By taking part in the program, you will be joining both national and international learners with the same passion for genetics. Interact directly with your Johns Hopkins instructors and fellow students throughout the program. Applications are now being reviewed for the Fall 2023 cohort, and a limited number of spots are still available.
PerkinElmer Genomics is a global leader in genetic testing focusing on rare diseases, inherited disorders, newborn screening, and hereditary cancer. Testing services support the full continuum of care from preconception and prenatal to neonatal, pediatric, and adult. Testing options include sequencing for targeted genes, multiple genes, the whole exome or genome, and copy number variations. Using a simple saliva or blood sample, PerkinElmer Genomics answers complex genetic questions that can proactively inform patient care and end the diagnostic odyssey for families. Learn more at PerkinElmerGenomics.com.
Picture Genetics is a new and unique DNA testing service powered by Fulgent Genetics. These tests are designed for every stage of life, from family planning and newborn health, to personal wellness and disease risk. Picture Genetics’ now also offers COVID-19 testing for easy testing without leaving your home. Unlike other companies, this is actually a clinical grade test where physicians and genetic counselors are involved. The test sequences entire genes that are medically actionable. It’s easy to order and understand with good looking reports! To order your Picture Genetics go to picturegenetics.com and use code “DNATODAY” for 25% off and free-shipping! Get actionable genetic insights today to benefit your family of tomorrow.
Imagine a health record system designed specifically for genomics. Cause let’s be honest, electronic health records are not built for genetics. Now you can stop imagining and start using, because PhenoTips is just this! PhenoTips is the world’s first complete genomic health record system. Now you can try it for free, just go to phenotips.com/signup.
You can also tune into their monthly international PhenoTips Speaker Series, hosted by Kira Dineen.
Do you work in a lab? Want to receive rewards when you order supplies? Check out Thermo Fisher Scientific’s Aspire program, it’s a rewards program created with scientists, like you, in mind. All members receive a free full size trial product every year. Points are earned every time you use or purchase products. Rewards include science themed apparel like a zip up DNA hoodie! Check it out at ThermoFisher.com/aspire-DNAtoday and for a limited time receive 500 bonus points. See the show notes for terms and conditions and that link.
ThermoFisher Terms and Conditions: Open only to eligible participants in the US (excluding Puerto Rico) and Canada (excluding Quebec). Eligible participants must complete the enrollment process for the Aspire member program in order to be enrolled in the program and receive rewards and benefits. Enrollees must confirm their health care professional or government employment status during time of enrollment. For full terms and conditions of the program, go to thermofisher.com/aspire/tc. Offer is void where prohibited, licensed, or restricted by federal, state, provincial, or local laws or regulation or agency/institutional policy. Other restrictions may apply.
The Illumina mission is to improve human health by unlocking the power of the genome. With Illumina’s sequencing-by-synthesis technology, they have only just begun to discover the true impact of genomics in areas including oncology, reproductive health, genetic disease, agriculture, microbiology, and beyond. Knowing the discoveries that lie ahead is what inspires Illumina to push the boundaries of their imagination and constantly drive innovation. To learn more by visiting illumina.com.
At the end of a busy day in the clinic, lab or classroom, the last thing you want to do is figure out dinner: what to make, actually cooking it, and doing the dishes. It all takes up too much time and energy to do every night.
Eating better is easy with Factor’s fresh, ready-to-eat meals. As some of you may know our host has been launching some new podcasts recently and these 2 minute meals have been a game changer during this busy time.
There are loads of different options weekly. All with no prep and no mess. And you can customize how many meals. And it’s less expensive than take out especially if you use our code, DNATODAY50.
What are you waiting for? Go check it out at factormeals.com/dnatoday50 to get 50% off. And let us know what your favorite meal is so we can try it out.
Discover the unparalleled precision of Wasatch Biolabs, your premier research and clinical lab service provider. With a focus on targeted DNA methylation analysis, Wasatch offers comprehensive genomic and cell-free DNA solutions. WBL’s services enable you to illuminate the nuances of native DNA sequence and methylation status at thousands of regions, delivering up to 750 kilobases of data per sample.
Their exclusive technology provides all the benefits of Oxford Nanopore Technologies native DNA sequencing—copy number identification, structural variance, methylation and hydroxymethylation status, etc.—at a fraction of the cost by honing in on regions of interest without amplification. Whether you're looking to quantify DNA, determine DNA cell of origin, multiplex multiple loci, or analyze hard-to-sequence genes, Wasatch BioLabs is your trusted partner for precision and accuracy.
In Episode 276 of DNA Today you can hear more about the technology and its applications directly from two of Wasatch Biolabs’s Co-Founders—CEO Chad Pollard and VP of Science and Technology Dr. Jonathon Hill.
Learn more about their innovative solutions at wasatchbiolabs.com. Go explore how Wasatch Biolabs can elevate your scientific endeavors.
As a listener of DNA Today, you probably heard me talk about NIPT, non-invasive prenatal screening, that looks for extra or missing chromosome conditions during pregnancy. But did you know there is one that can also screen for recessive disorders (like cystic fibrosis) and fetal antigens?
BillionToOne offers UNITY Screen, which does all this from one blood draw from a pregnant person.
Visit unityscreen.com for more info. And stay tuned for our upcoming episodes with BillionToOne exploring non-invasive prenatal screening for recessive conditions and red blood cell fetal antigens!
As a listener of DNA Today you have heard me interview countless guests about genetic testing. I’m sure you have thought to yourself, “I wonder what my results would be”.
Now you can find out or gift it to someone else! At Panacea, you can access affordable Whole Exome Sequencing, that’s analyzing all of your coding genes, genetic counseling and physician oversight in a 10-minute workflow for under $1000.
As a DNA Today listener you get 30% off (that’s a $300 discount), just use the code “DNATODAY” at seekpanacea.com. Again that’s code “DNATODAY” at seekpanacea.com for $300 off. The link is also in the show notes.
The show receives a lot of emails from listeners interested in genetic careers and we love connecting and providing resources. One of those is Keck Graduate Institute’s genetics programs in Southern California. KGI offers a master’s degree in genetic counseling, but for those of you looking for something slightly different - KGI also has a first-of-its-kind graduate program in genomic data analytics. This two-year master’s program gives students the opportunity to work side-by-side with applied life scientists and future genetic counselors while gaining hands-on experience with the technologies and information that are revolutionizing the future of medicine. Learn more about the program by visiting kgi.edu/dnatoday.
Have you heard of the Blueprint Genetics My Retina Tracker Program? This program offers eligible patients in the US no-cost comprehensive genetic testing and counseling for their inherited retinal degeneration. The My Retina Tracker Program Panel includes 351 genes, mitochondrial DNA, and non-coding variant assessment. Stay tuned for our interview with Blueprint Genetics about the My Retina Tracker Program on May 13th, 2022 of DNA Today. In the meantime, you can learn more at BlueprintGenetics.com.
If you’ve been listening to DNA Today for a while, you probably know our host Kira Dineen is also a full time prenatal genetic counselor. Between that job, this podcast, and being a producer/host of other podcasts, she is pretty busy! To keep her energy up and stay productive she drinka a decent amount of coffee. The new coffee she is drinking is from Four Sigmatic. She is really picky about her coffee, it’s got to be bold, not watery. And she has been really happy with Four Sigmatic.
Here’s the difference from other coffees, it includes mushrooms, which I know sounds bizarre. We will admit we were hesitant, but you get health benefits and don’t taste it. We like the immune system boost. So we teamed up with Four Sigmatic to get you 30% off using promo code “DNATODAY” redeem it at FourSigmatic.com, again that’s FourSigmatic.com using code “DNATODAY” for 30% off! And let us know if you like it too!
Every pregnancy has a chance to have a genetic abnormality or complication. Mitera empowers you to make the most informed reproductive decisions through their at-home genetic tests, without needing your doctor’s order. These tests include non-invasive prenatal screening (Mitera’s Peaches&Me) and carrier screening (Mitera’s 23pears). Our host Kira did the 23pears kit and discovered she is a carrier of a condition. Request your own kit at miteragenetics.com and use code “DNATODAY” for 10% off. Mitera. Predict. Prevent. Prepare.
Are you seeking a career with purpose in the healthcare space? We recommend checking out Worldwide Clinical Trials, a contract research organization that partners with pharmaceutical and biotechnology companies to advance development of new medicines. Apply your passion at Worldwide where they take an entrepreneurial approach backed by scientific expertise to help bring treatment options to patients. With a global team of 3,000 experts, you will be inspired by bright thinkers, dreamers and doers who innovate and invent for a brighter tomorrow. Perks include unlimited flexible paid time off, limited travel requirements, and the ability to work remotely. Bring your talents and passion and join the team at worldwide.com.
Do you want to connect with other people who have the same genetic variant as you? You should check out “Connect My Variant”, it’s an online resource that allows you to do just that. “Connect My Variant” also provides different avenues of informing your family of possible inherited risk of disease. This includes helping find where your variant came from and finding distant cousins that may also be at risk. The University of Washington has supported the “Connect My Variant” project in an effort to help patients and families understand where their unique genetic variants come from. Check out it at ConnectMyVariant.org.
Do you or someone you know have Prader-Willi syndrome? Harmony Biosciences is looking for people with Prader-Willi syndrome to enroll in a new clinical study in the United States. Harmony Biosciences will be studying the safety and impact of an investigational medication on excessive daytime sleepiness, cognition, and behavioral function in people with Prader Willi syndrome. Learn more about the clinical study and refer a patient to a study center here.
Vizgen is dedicated to pioneering the next generation of genomics, providing tools that demonstrate the possibilities of in situ single cell spatial genomics. These tools are enabling researchers to gain insight into the biological systems that govern human health and disease. Stay tuned for our full episode with Vizgen where we explore single-cell spatial genomics. Get a sneak peak by visiting their website at vizgen.com. Vizgen, leaders in spatially resolved, single-cell transcriptomics.
Did you know that most cancer samples cannot be subjected to some of the most common cytogenetic analyses due to their storage in formalin and other intractable storage conditions? Don’t let difficult sample types and convoluted assay cascades get in the way of your research! Phase Genomics has developed a brand new Next Generation Cytogenomics platform to advance discovery in reproductive genetics and precision oncology. A single assay has the ability to do comprehensive testing for chromosomal abnormalities in fresh, frozen, AND even paraffin-embedded FFPE samples. Learn more about Phase Genomics’ incredible new platform in cytogenomics by visiting PhaseGenomics.com. You can also hear our in depth interview with them on Episode 169 of DNA Today released on January 28th, 2022.
Aceragen is a rare disease biopharmaceutical company. Aceragen takes on rare, orphan diseases that typically have no approved treatments, and works to develop therapies to help patients. The needs of patients who suffer from under-served rare diseases drive Aceragen’s mission. Be sure to tune into our episode with Aceragen in February 2022 as we celebrate rare disease month! Learn more at aceragen.com. Aceragen working for a better life for patients with rare diseases.
If you’re a healthcare provider helping pregnant patients you have inevitably been asked the question, “Can I take this medication during my pregnancy”? Then you need TERIS, a clinical electronic resource that contains information on the teratogenic risks of over 1,700 medications and other environmental exposures and infections, including 200 of the most frequently prescribed drugs. What makes TERIS (Teratogen Information System) a unique database? TERIS is governed by an Advisory Board of world-renowned experts in clinical teratology and is an intellectual property of the University of Washington. Visit TERIS today and use code “DNAToday” for your free no obligation 2-week evaluation license.
Genomenon is an AI-driven genomics company dedicated to improving the lives of patients with rare genetic diseases and cancer. Genomenon’s Genomic Landscapes help pharma and biopharma gain profound insight into the molecular drivers of disease to accelerate progress through all stages of the drug development process. Look out for our October 1st episode – the founder of Genomenon will be a guest on DNA Today to explore the genetics of ALS. Learn more about Genomenon here.
Want to chat with genetic counselors? You should attend the virtual open houses at Sarah Lawrence College! In these events you can learn what it’s like to be a genetic counselor. And you will have the opportunity to ask your questions live!
You can also hear insight about the Genetic Counseling Master’s degree program at Sarah Lawrence College. It is the largest program in the world. Which means there are so many alumni to connect with, including myself. I graduated from the program last year and am really looking forward to chatting with you! The next open house is on October 28th followed by December 7th.
Go to SLC.edu/DNAtoday, to sign up for the free genetic counseling open houses. Our host Kira Dineen will see you there!
If you enjoy DNA Today you will also love Eureka’s Sounds of Science, a podcast from Charles River. Sounds of Science tells the stories of how – how chicken eggs impact vaccine development; how a single parent can change the FDA; how a horseshoe crab saves lives. If you enjoyed our episode (#74) with Huntington Disease patient advocate Antonio Maltese, you should check him out in this episode of Eureka’s Sounds of Science podcast! Listen to Eureka’s Sounds of Science on Apple Podcasts, Spotify, or wherever you download your podcasts.
Do you work in cytogenetics? Thinking about applying to new jobs? Well I found a great position for you at UNC Health. In this Senior Cytogenetic Technologist position you will join a team of 20 fellow technologists and specialists. The Cytogenetics Lab at UNC Health performs prenatal, postnatal, and cancer cytogenetic testing on about 5,000 cases every year and you have the opportunity to perform conventional cytogenetics, FISH and microarray testing.
Unfortunately, not everyone has access to see a genetic counselor in person, this has always been a barrier in our field. That’s why Elizabeth Turner started Advanced Tele-Genetic Counseling in 2016, to be able to provide a scalable telehealth platform for genetic counseling services, where genetic counselors can help patients navigate through areas of genetics like genetic testing, and ultimately understand their own genetics.
Their multidisciplinary approach to genetic counseling makes AT-GC a great fit for patients and their providers. So if you find yourself having questions about your own genetics, or want to know more about adding the expertise of AT-GC’s certified genetic counselors to help support your own practice, reach out to the team through their website at at-gc.com.
Did you know most people are visual learners? That’s why visual aids are critical during genetic counseling appointments. As we explore in this show, genetic concepts can be really complex to understand, which is why the Greenwood Genetic Center created genetic counseling aids. And now their 7th edition is available, including an app for iPads. In telehealth appointments it can be incredibly helpful to share your screen with these visual aids from Greenwood, so head over to ggc.org/publications to download this vital tool for your daily practice.
LetsGetChecked offers home testing kits for sexual health, men's health, women's health and general wellness. A kit gets sent discretely to your place, you collect a sample and send it back in the mail. Your results are available through the website and you receive a call from a nurse to go through your results! Our host Kira did their female fertility test to help her understand my hormonal health. For 20% off your own kit use code “DNAToday” at checkout on LetsGetChecked.com.
How do you keep research articles organized? We have struggled with this for years, but have finally found a solution that is simple and easy. It’s called Paperpile! It radically simplifies the workflow of collecting, managing and writing papers. Paperpile allows you to highlight and annotate papers, manage references, share and collaborate and even cite directly in Google Docs and Microsoft Word. Paperpile’s new mobile apps allows you to sync your library to all your devices so you can read and annotate on your iPad, iPhone, or Android device. Start your free 30 day trial today at paperpile.com with promo code “DNATODAY”. Paperpile costs only $36 per year, but with code “DNATODAY” you save 20%!
The Parkinson's Foundation makes life better for people with Parkinson’s disease by improving care and advancing research toward a cure. In everything we do, we build on the energy, experience and passion of our global Parkinson's community. PD GENEration: Mapping the Future of Parkinson’s Disease is a Parkinson’s Foundation initiative that offers genetic testing and genetic counseling at no cost for people with Parkinson’s disease (PD). When you participate, you can help scientists in their journey to advance understanding of PD, leading to new, more effective PD therapies. Enroll here for the PD GENEration study.
Healthy Davis Together is a joint project between the City of Davis and UC Davis with a goal to prevent the spread of COVID-19 and facilitate a coordinated and gradual return to regular city activities and reintegration of UC Davis students back into the Davis community. Learn more in this DNA Today podcast episode with Healthy Davis Together representatives who share insight on COVID-19 variants. You can also check out the Healthy Davis Together website.
BioVaxys is a clinical-stage biopharma developing antiviral and anticancer vaccine platforms. BioVaxys is evaluating a potential SARS-CoV-2 vaccine based on its haptenized viral protein technology, and advancing a compassionate use trial in the EU to evaluate its haptenized cell vaccine for late-stage ovarian cancer. Learn more in their DNA Today interview in this podcast episode. You can also check out their website.
Did you do a direct-to-consumer test? Maybe you are confused and scared what the results could mean? Instead of going to Dr. Google, you can speak to a certified Genetic Counselor. And now I have a new resource for you, DNA Ally. Think of them as your genetic counselor matchmaker. For $79 you can book a 20 minute session with a certified genetic counselor to answer your burning questions. DNA Ally is giving DNA Today listeners a discount. Use code “DNAToday” at checkout for 15% off that original $79, so that’s $67 for your session. Replace confusion with clarity, go to DNAally.com and decode your DNA test results.
Early genetic screening is an important step in planning for a healthy family. Get a comprehensive, affordable genetic test at-home. Available in all states at the price of $149 with insurance. Bonus, there is free genetic counseling. Learn more and request your kit now at Jscreen.org.
GenoBank is the first anonymous DNA storage and sharing platform. GenoBank allows you to participate in the Genomic Revolution with maximized privacy through Blockchain Networks to keep track of all the data sets and Genomic Reports without exposing your personal data (and your family’s data)! GenoBank creates a way for you to decide who has access to your genetic information. The aspect we are most intrigued by is how you can take part in research to further science by choosing specific institutions and even projects to contribute your DNA. Check it out at genobank.io.
The practice of genomic counselling and variant interpretation is advancing at an incredible pace. The University of British Columbia offers an online, flexible graduate certificate for genetic professionals who want to keep up. You will learn to apply the latest methods in clinical bioinformatics, variant interpretation, and genomic counselling. It’s an ideal way to earn CEUs while enhancing your genetic counselling practice. Learn more and register on their website.
Do you want to influence change in the genomics market? Lucky for you a new position just opened at Agilent where you can have an impact as a Genomic Software Field Applications Scientist. In this west coast remote-based role you will provide technical consultation, training, and education to enable customers to perform data analysis in clinical laboratory environments. You will partner with sales to serve as the scientific/technical specialist to help drive sales and provide support for customers in diverse clinical settings. Learn more about the position and submit your application here.
Did you know there is a genetic counselor that specializes in offering care to those in the adoptee community? Brianne Kirkpatrick cowrote “The DNA Guide for Adoptees” to provide a resource for those in the adoptee community who are utilizing DNA testing to find biological relatives or to seek out medical information. She also started Watershed DNA to offer personalized genetic counseling to directly support people in the aftermath of a surprise DNA discovery. You can hear Brianne share her insight from her book in Episode 56 and Episode 103 of DNA Today! Learn more at WatershedDNA.com where you can also book your consult today with Brianne.
Variant classification and interpretation have become important skills for genetic counselors. But it takes so long! Even if it’s just a VUS you want to double check. To make it streamlined check out franklin.genoox.com/DNAToday. You can access so much information about a variant including relevant publications, automated ACMG classifications, annotations and phenotypes/disease. Best part? It’s free! All this data about one variant is compiled at your fingertips. No more sifting through PubMed! Join the future of variant interpretation.
Precipio's platform delivers superior diagnostic accuracy through academic expertise and cutting edge technology. Precipio is a laboratory focused on delivering specialized diagnostic services to physicians and their patients to ensure they receive accurate results. Learn more on their website, PrecipioDX.com.
How do you like spending the summer? In my free time I am usually with friends at our apartment’s pool. My spot is right next to the water reading a book, most recently A Crack In Creation, which might come up in a future episode. I like keeping cool by sipping on some ice tea while I read, but I don’t like all the sugar. So I’ve been enjoying Sound drinks instead. Sound makes unsweetened, organic sparkling waters made with tea and botanicals. No natural flavors or sugar.
My fav is the blueberry with cinnamon and hibiscus tea. Try it out by ordering at DrinkSound.com using promo code DNATODAY for 20% off, plus you are supporting the podcast!
A bunch of my friends in my apartment complex have dogs and I love being able to offer them a treat when I take them for a walk or they visit my place. So I got Sundays for Dogs.
Now this is dog food, but can also be used as dog treats. My friend Annie’s dog, Frank, gets so excited when he sees me, and if I’m being honest, I think it’s more the food than me. Sundays For Dogs is real food formulated by a Vet with high quality meat, veggies, fruit and superfoods, then air-dried to perfection.
Since you are a DNA Today listener, you can visit SundaysForDogs.com and use code “DNATODAY” for 35% off your first order. Support your pup and the podcast!
Curious and want to try a DNA test, but concerned about your genetic data being shared? Secret Sequence is an anonymous genetic testing company, you never give your name for any reason. So they do not sell or share your data, unlike other companies. Secret Sequence offer various tests including ancestry, nutrition and exercise. For $25 off two kits or more head over to SecretSequence.com and use promo code “DNAToday”.