MyOme’s Post

Genomes2People director Dr. Robert Green MD, MPH spoke on 'Newborn Sequencing' at the Critical Assessment of Genome Interpretation (CAGI) workshop at the Northeastern University, Boston today. Newborn sequencing plays a pivotal role in modern healthcare by offering insights into a baby's genetic makeup. It can identify potential genetic disorders and conditions early on, enabling timely interventions and personalized treatments. #conference #workshop #scienceconference #biology #genetics #dna #genes #genome #genomics #preventivegenomics #computationalbiology #computationalgenome #research #science #newborn #sequencing #genomesequencing #newbornhealth #publichealth #health #precisionhealth #medicine #precisionmedicine #healthcare

Are you attending the ACMG - American College of Medical Genetics and Genomics 2024 Annual Conference? Visit MyOme’s booth #627D to hear about our latest updates: - Discover how we are seeking to help reduce the diagnostic odyssey for neurodevelopmental delays,  and how you can be a part of the solution.  - Learn how our offerings provide comprehensive solutions to population health studies. While at our booth, enter our raffle for a chance to win a complimentary MyOme Personal Genome™, a clinical-grade, whole genome sequencing test, which includes a Proactive Health Report and a Pharmacogenomics Report, as well as a one-on-one genetic counseling session. Once you’re on the MyOme Personal Genome™ platform, you will be notified of additional reports when they become available. Learn more about the MyOme Personal Genome™ test at myome.com. Want to spend more dedicated time learning how we can potentially partner? Contact us at support@myome.com to set up a ☕️ meeting. Looking forward to seeing you in Toronto! #acmgmtg24 #neurodevelopmentaldelay #populationhealth #pgx #phr #screening #diagnotictesting #precisiononcology #wgs #genome #genetics #genomesequencing #wholegenomesequencing #healthtech #healthcare #health #precisionmedicine #precisionhealth #genes #science #dna #dnasequencing #dnatesting #dnatest #biotech #familyhealth #hereditarycancer #pharmacogenetics #pharmacogenomics #familymedicine #conciergemedicine #myome

Translational Genomics: Unraveling the Genetic Basis of Common and Complex Diseases #clinicalgenetics #genomicresearch #healthcare #humangenetics #medicalgenetics #medicine #precisionmedicine #translationalgenomics

𝐂𝐚𝐫𝐫𝐢𝐞𝐫 𝐒𝐜𝐫𝐞𝐞𝐧𝐢𝐧𝐠 𝐌𝐚𝐫𝐤𝐞𝐭 𝐒𝐢𝐳𝐞 𝐭𝐨 𝐑𝐞𝐚𝐜𝐡 $𝟓.𝟒 𝐁𝐢𝐥𝐥𝐢𝐨𝐧 𝐛𝐲 𝟐𝟎𝟐𝟖 𝐃𝐨𝐰𝐧𝐥𝐨𝐚𝐝 𝐏𝐃𝐅 𝐒𝐚𝐦𝐩𝐥𝐞 𝐑𝐞𝐩𝐨𝐫𝐭: https://lnkd.in/d5mfDrVB The size of global carrier screening market in terms of revenue was estimated to be worth $2.2 Billion in 2023 and is poised to reach $5.4 Billion by 2028, growing at a CAGR of 19.7% from 2023 to 2028. 𝐊𝐞𝐲 𝐏𝐥𝐚𝐲𝐞𝐫𝐬: Good Start Genetics Bioarray Genetic Diagnosis The Allied Group. IGENOMIX UK Picture Genetics Repromed South Genetics, Inc. Jetanin Hospital Neoscreen Medical Ltd Advanced Testing in Clinical Genetics Lumi Health AU TAGmedica Miragenex CellGenetics Noor Thalassemia Foundation #CarrierScreening, #GeneticTesting, #HealthcareInnovation, #PrenatalCare, #MedicalResearch #carrierscreeningmarket

#G2PSpotlight: Thomas Minten, Ph.D. (mentored by Dr. Nina Gold) presented on "Exploring heterogeneity among gene lists proposed for newborn sequencing," at ACMG - American College of Medical Genetics and Genomics #ACMGMtg24. You can read the research study here: https://lnkd.in/gE6PxvvG #research #healthresearch #translationalresearch #science #genetics #dna #genes #geneticresearch #genome #genomics #preventivegenomics #translationgenomics #genomicresearch #screening #sequencing #genetictest #genetictesting #geneticcounseling #newbornscreening #newbornsequencing #health #newbornhealth #childhealth #publichealth #populationhealth #precisionhealth #preventivehealth #preventativehealth #futureofhealth #personalizedhealth #healthcare #newbornhealthcare #childrenhealthcare #preventivehealthcare #preventativehealthcare #personalizedhealthcare #medicine #precisionmedicine #genomicmedicine #preventivemedicine #preventativemedicine #personalizedmedicine #clinicalresearch #futureofhealthcare #healthcareinnovation #futureofmedicine #healthcommunication #posterpresentation #healthcareconference #toronto #sciencecommunication #scicomm

Here's what we've heard are current hot topics dominating the biopharma news cycle as we head into 2024: - Obesity and diabetes - Genomic medicine - Microbiome - Synthetic biology - Neuro-tech - Reproductive tech - Bioethics - Industry financing and business models in current climate ⬇️ Tune in below for our first highlights reel from #TicketToBiotech's recent Press Pass panel. What else would you add to this list?

In the latest issue of The Journal of Perinatology-Neonatology, Madhuri Hegde, Senior Vice President and Chief Scientific Officer at #Revvity, delves into the cost-effective potential of employing first-line Whole Genome Sequencing to diagnose #genetic conditions in children. The aim? Minimizing delays and expediting prompt treatments. Check out the insightful article on Pages 32-33 Link: http://ms.spr.ly/6042cb9ou

Integrating genetics into primary care is crucial. There are four key areas where genetics can make a real difference for patients across their lifespan. The #1 way genetic insights help: MANAGING MEDICATIONS AND SIDE EFFECTS Researchers have found that your genes influence how you respond to different drugs. Genetic variations affect the way you absorb, distribute, metabolize and eliminate medicine from your body. These variations impact medication effectiveness and safety. By collaborating with a geneticist to obtain pharmacogenomic information, healthcare providers can tailor the dosage and choice of medication to your DNA. This can help optimize treatment plans and overall outcomes. To learn more about genetics and primary care, check out our article on the topic: https://lnkd.in/eh6-VuGC #genetictesting #genetics #sequencemd #caremanagement #diagnosis #raredisorders #neurogenetic #raregeneticdisorders #metabolicconditions #chromosome15 #geneticdisorders #AngelmanSyndrome #Duplication15q #PraderWillisyndrome #primarycare #medicationsideeffects #DNA

🌐🔬The evolution of medicine is ahead of all expectations thanks to new technologies for analysing and editing the genome. 🧬✨ 🔍 Genome analysis allows us to look into the very core of our DNA, revealing information about our genetic predispositions to various diseases. This is the key to early detection and prevention of many diseases. 🛠️ Genome editing, including CRISPR technologies, offers the potential to alter our genetics, providing a unique opportunity to correct defective genes and fight inherited diseases. These innovations have the potential to change the face of medicine, making it more accurate and effective. They could help treat a range of diseases, from rare genetic disorders to oncology, as well as contribute to a better understanding of human biology.🩺🙌🏻 #medicaljobs #HealthcareJobs #MedicalCareer #vacancies #medicine #medicalfield #MedicalRecruitment #healthcare #genetics #genome #technologies

New algorithm could improve the search for genetic cause of hereditary diseases. Variations of genetic sequence occur relatively frequently on average, one in a thousand nucleotide of a person's genome is affected. In rare cases, these changes can lead to defective RNAs and hence non functional proteins. This can lead to dysfunction in individual organs. If a rare disease is suspected, computer-assisted diagnosis programs can help in the search for possible genetic causes. Specifically the genome can be analyzed using algorithms to find out whether there is a connection between rare genetic variations and dysfunctions in specific parts of the body. Submissions are open for the upcoming issue. You may submit case reports, case studies, and research or review papers. Submit to: editor.geneticsandheredity@journalmaples.org Follow our page: https://lnkd.in/dd-AwMD8 Visit us: https://lnkd.in/dhyieEcT (Source: internet) #genetic #heredity #research #genes #genomics #algorithm #geneticsequence #diagnosis #submissions #openaccess