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    Charles G. Mullighan, MBBS (Hons), MSc, MD-Member, St. Jude Faculty-Deputy Director, Comprehensive Cancer Center-St. Jude Children’s Research Hospital Charles Mullighan, MD, delves into the genomic classification of Acute Lymphoblastic Leukemia (ALL) and its diagnostic approaches. He covers three main area…

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    • Explore Acute Lymphoblastic Leukemia insights by Charles Mullighan, MD! Learn about genomic classification, diagnostics, and more. 🧬 #ALL #Genomics [slides][video] https://t.co/2aoU8Ienvu ➡️ @_MDEducation @Ryan_fitzpatric https://t.co/bP0utDRKlF

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    Uncover your genetic health and potential risks with Bioaro’s comprehensive genomic testing. Book your test now and take control of your health with personalized insights and recommendations.

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    • Make sure to check @macleans Let’s beat Cancer! Get Tested with #BioAro Get WHOLE DNA analyzed, Know YOUR Whole Book 📖. https://t.co/CWqVk4LUqm @BioAroInc @MediaplanetCA #Macleans #Genomics #PrecisionHealth #BioInformatics #Cancer #CancerCare #MensHealth… https://t.co/F9ahA86cNj https://t.co/GguSHEktS7

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    Register to attend in person Register to attend virtually

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    • The ICR's Professor Paul Workman is speaking today at the Karolinska Institutet (@karolinskainst) about 'the promise and perils of #ChemicalProbes', to celebrate 20 years of the Structural #Genomics Consortium (@thesgconline). More information here⬇️ https://t.co/ErW1QACN7J https://t.co/9ktrqi30T8

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    The mission of the Public Health Genomics is to integrate advances in human genetics into public health research, policy, and programs

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    • Check out #HLBS-PopOmics: an online, continuously updated, searchable database of published scientific literature. @CDCgov @NIH resources & other materials on the translation of #Genomics and other #Precision Health discoveries into improved health. https://t.co/U73IrHmEdA #CTRIS https://t.co/Y2GU6NK4rA

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    Nature Genetics – A modified framework leveraging a protein language model (ESM1b) is used to predict all possible 450 million missense variant effects in the human genome and shows potential for…

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    • THIS ROCKS: #Genome-wide prediction of #disease variant effects with a deep protein language model https://t.co/X6IwVMRHvv #Genetics #Genomics #ClinVar #HGMD Advancing #variant effect prediction using protein language models https://t.co/KuI085HUJ4 #pathogenic #SNV/#SNP… https://t.co/lT0TnZv0EK https://t.co/cwI5AWqxqb

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    Northwestern Medicine investigators led by Ruli Gao, PhD, have developed a novel genetic sequencing tool that accelerates sequencing analysis of same-cell genotypes and phenotypes in tumors, as detailed in a study published in Nature Communications.

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    • Investigators led by @LurieCancer member @Ruli_Gao have developed scNanoGPS, a novel genetic sequencing tool that accelerates analysis of same-cell genotypes and tumor phenotypes, detailed in @NatureComms. https://t.co/FUkPSMGHvV via @NUFeinbergMed #genomics