Devyser’s Post

Did you know that Carepoint Labs offers top-notch cytogenetic services? Whether you're in need of comprehensive genetic testing or exploring chromosomal abnormalities, Carepoint Labs has you covered. Learn more about our cytogenetic services and how we can assist you on our website. Trust Carepoint Labs for accurate results and expert care in genetic testing! #CarepointLab #GeneticTesting #Atlanta

Hereditary Genetic Testing Market to Soar to $81.95 Billion by 2033: BIS Research https://lnkd.in/eWV5D86Z #marketanalysis #marketresearch #marketresearchreports #businessintelligence

Our paper on genetic testing of VEXAS syndrome has recently been published. You can read the paper and let us know if you have the testing needs. #vexas #xna #luminex https://lnkd.in/g4egwu9h

Did you miss the recent Devyser webinar with Dr. Robert Akkers highlighting the shifting distribution of hemoglobinopathy and the need for expanded thalassemia genetic testing? Now watch the on-demand webinar here: https://bit.ly/3RPitjr #thalassemia #ngs #genetictesting

New Episode of ASN Kidney Translation with @Nephro_Sparks @ASNKidney Genetic Testing in Nephrology: Topics include genetic testing in CKD, MUC1 ADTKD screening, and digenic Alport syndrome insights https://lnkd.in/e2gFnjAq

August is Spinal Muscular Atrophy (SMA) awareness month! 1 in 50 people are a carrier for SMA and the only way to learn your carrier status is through genetic screening. #GeneticTesting #GeneticScreening #SMA #SpinalMuscularAtrophy #GetJScreened #CancerGeneticTesting

Clinician-led reanalysis of exome sequencing (ES) data significantly improves the diagnostic yield for patients with inherited retinal disease (IRD), identifying additional genetic causes that were missed in initial genetic testing, according to a study. Read the complete article below ⤵️ #GeneticTesting #IRD #InheritedRetinalDisease

Polygenic risk scores (PRSs) are estimates of an individual's susceptibility to a specific complex trait obtained by aggregating the effects of dozens, thousands, and potentially millions of genetic variants associated with that specific trait into a single figure. Some private companies now market PRS embryo screening to prospective parents through the use of in vitro fertilization and pre-implantation genetic testing.

Cornelia de Lange Syndrome (CdLS) is a congenital genetic disorder typically stemming from de novo variants rather than inheritance. Its etiology commonly involves variations in one of seven genes occurring at or shortly after conception. Genetic testing can help aid in the diagnosis of this syndrome. Learn more about our CdLS Panel here: https://ow.ly/7g6F50Ro98w

🧪✨ Stay informed on the latest innovations and best practices in genetic testing! This comprehensive seminar will help guide professionals through the different steps of the Preimplantation Genetic Testing (PGT) process, from the initial intake of patients to successful post-procedure follow-up. During the two-day programme, you will learn about: 💠 Tips and tricks for PGT sampling 💠 Before and after PGT 💠 Evaluation of PGT technology for all indications – lessons learnt 💠 Embryo transfer policies 💠 New trends in PGT You'll also have the opportunity to submit your questions or case reports in advance for discussion during the panel sessions following each presentation. Do you have a question or a report you would like discussed? Make sure to register and send in your submissions! 📑 Registration is required for both in person or virtual participation: find out all details on 🔗https://lnkd.in/empMfcBX #ESHRE #PGTConsortium #PGTSeminar2024