Top Tweets for #vus
VUS: ¿Avance o maquillaje? 🤔
Digitalizar solo la cita no es transformación digital real. Es hora de que en Bogotá la tecnología sirva para eliminar la presencialidad innecesaria.
Comenta tu experiencia con la VUS. 👇
#DirectoYClaro #MovilidadBogotá #VUS
Valle Umbra Servizi, ok a bilancio 2025: 47 milioni di euro di investimenti https://t.co/OZDCDFK3rz
#tuttoggi #ComunicatiStampa #EconomiaLavoro #Foligno #bilancio #evidenza #scoop #valleumbraservizi #vus
Variants of uncertain significance (VUS) remain one of the most challenging aspects of genetic testing. ACMG's new Points to Consider statement provides evidence-based recommendations to support consistent reporting and interpretation. https://t.co/E18xQUtUlJ #VUS
Not everyone undergoing #genetictesting will receive a clear result - sometimes they find an alteration in a gene but don't yet know enough about the specific alteration to determine if it causes disease or not. This is known as a #VUS - a variant of unknown significance 🧐👇
𝐖𝐡𝐞𝐧 "𝐖𝐞 𝐃𝐨𝐧'𝐭 𝐊𝐧𝐨𝐰" 𝐈𝐬 𝐭𝐡𝐞 𝐌𝐨𝐬𝐭 𝐑𝐞𝐬𝐩𝐨𝐧𝐬𝐢𝐛𝐥𝐞 𝐀𝐧𝐬𝐰𝐞𝐫 𝐢𝐧 𝐆𝐞𝐧𝐨𝐦𝐢𝐜𝐬 https://t.co/6lsEmIcYzf via @lynchsyndromirl
Struggling with tricky variants in rare neurodevelopmental disorders?
We unpacked 3 real cases in Horizon Series:
🧬 TCF4 – broader phenotypes
🧬KCNH1 - G6PD focal epilepsy
🧬KMT2D – Kabuki syndrome
Long-read genomics delivering answers.
#raredisease #Genomics #VUS #Gene
To resolve VUS variants, Horizon Variant Knowledgebase provides global open access to additional insights with identical variants.
Search your VUS (SNV, Indel, SVs) to gain more insights:
https://t.co/HxscsoBmHs
#VUS #rarediseases #Genome #Gene
Search any variant to learn about their ACMG or AMP pathogenicity for #raredisease or #cancer This is free to use, and includes SNV, indels, and SVs, with non-coding annotations as well.
Horizon variant search server: https://t.co/HxscsoBmHs
#rarediseases #cancer #genome #VUS
Don’t ignore the #VUS. High-risk VUS in genes associated with hereditary thoracic aortic disease strongly associated with aortic dissection. https://t.co/ul9ZwPaTlx #aortopathy #TAAD
Yök başkanımızdan güzel bir tespit
Doktoralı veteriner hekimlerin uzmanlık ve tecrübeleri heba edilmemeli.
#veterinerhekim
#onehealth
#teksağlık
#vus
#farmakoloji
#tarımveorman
#veterinerhekimsenyıpranırsın
Tarım ve Orman Bakan Yardımcısı sayın @AhmetGumen ile Veteriner Hekimliğinde Uzmanlık Kurulu üyelerini Yükseköğretim Kurulumuzda ağırladık.
Görüşmemizde, başta veteriner hekimliğinde uzmanlık eğitimi olmak üzere, Tarım ve Orman Bakanlığı ile Yükseköğretim Kurulu arasında, Bakanlığın ihtiyaç duyduğu konularda üniversitelerimizde araştırmaların yapılması ve projelerin geliştirilmesi, Bakanlık bünyesinde çalışan doktoralı uzman personelin 2547 sayılı Kanunun Ek/46. Maddesi kapsamında üniversitelerimizde görevlendirilmeleri üzerine değerlendirmelerde bulunduk.
Introducing TopoGrammar: Cracking the "VUS" Code with 3D Genomics & Blockchain
68% of identified ##genomic variants are currently classified as "Variants of Uncertain Significance" (#VUS). For patients, this means a #diagnostic dead end.
The Problem: Conventional sequencing misses "balanced" structural variants, inversions and translocations that don't change gene dosage but do wreck the genome's 3D regulatory architecture.
The Solution: #TopoGrammar treats chromatin organization as a structured language. By modeling enhancers and promoters as "grammatical sentences," we identify disruptions that others miss.
The Tech:🧬 PINNs: Physics-informed neural networks for high-fidelity 3D reconstruction. 🎯
- CTCF-Gating: 91% boundary detection accuracy (outperforming HiCCUPS). ⛓️ #Blockchain
- Attestation: Every result is hashed to the #BSV blockchain for immutable, @US_FDA-compliant verification without exposing PHI.
The Results:• 68% VUS reclassification rate. • 93% pathogenic accuracy. • Seamless integration with @BioPrimeAI v4.0 for genome-to-drug workflows.
Stop guessing on VUS. Start decoding the #3Dgenome.
🔗 Try the Live Demo: https://t.co/EEUuiIdHWL
@SmartLedgerTech @bioprimeai @Sdot2121 @Codenlighten1 @jalexanderm @grok
#Genomics #PrecisionMedicine #AI #Biotech
VUS celebrated Saraswati Puja with reverence and devotion, seeking the blessings of Goddess Saraswati for wisdom, knowledge, and enlightenment. The celebration reflected our collective respect for learning, culture, and tradition.
#SaraswatiPuja #VUS #Knowledge #Wisdom
❓ What’s a Variant of Uncertain Significance (VUS)?
A VUS may appear in genetic testing, but it’s NOT actionable on its own!
Always interpret VUS results with a phenotype-driven approach and family context. 🧠
#VUS #Genetics #CardiologyTips
Impressive talk by Dustin Baldridge tackling one of the biggest challenges in genomics: variants of uncertain significance. Deep mutational scanning is pushing us toward real answers — and real clinical impact. Powerful stuff. 🧬🔥#PPI #VUS @WashUMedGen @WashUMedPeds #Genetics
C. elegans model enables rapid reclassification of FH gene variants, offering a powerful tool to interpret #VUS and improve diagnosis in FH-associated metabolic diseases. https://t.co/yA2zb81tB2 #GIMO #FHfum1 #ClinicalVariant #CRISPR #VariantClassification #ClinicalDiagnosis
Rare #ARID2 variants cause a #neurodevelopmental disorder with developmental delay, ID, behavioural issues, and dysmorphic features.
A unique DNA methylation episignature may help reclassify #VUS and refine diagnosis.
https://t.co/bGZW86Ubvh
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