Top Tweets for #NGStesting
We’ve been talking about why NGS matters. Now I want to hear from you. What is your BIGGEST barrier to ordering NGS testing for your patients?
#DecodeTheCancer #CancerFax #NGSTesting #PrecisionOncology #OncologyEducation #CancerCareIndia
ಕ್ಯಾನ್ಸರ್ ಚಿಕಿತ್ಸೆಯಲ್ಲಿ ಆಧುನಿಕ ತಂತ್ರಜ್ಞಾನ: ಒಂದು ಹೊಸ ಭರವಸೆ
A decade ago, most cancers were treated with similar chemotherapy.
Today, molecular testing and NGS guide personalized treatment decisions.
#KIMSMACS #KIMS #MACSclinic #DrSandeepNayak #NGSTesting #GeneticTesting
On Jan. 29: Explore the hybrid approach for #NGStesting that combines rigorous expert curation & fast AI workflows. See how HGMD Pro’s integration with Franklin accelerates actionable #hereditarydisease insights. Save your seat 👉 https://t.co/cL0AzJlRPC
BREAKWATER - BRAFV600Emt mCRC
EC-FOLFIRI has now joined EC-FOLFOX
#BRAFV600E #NGStesting #Genomic
#mCRC
At #ASCOGI26, BREAKWATER extends targeted therapy into the FOLFIRI backbone for BRAFV600E-mutant mCRC.
Encorafenib + Cetuximab + FOLFIRI vs FOLFIRI + Bevacizumab (1L)
Toxicity was not worse than control, and treatment exposure was longer.
This does not replace EC + mFOLFOX6 for everyone.
But for patients unsuitable for prolonged oxaliplatin (neuropathy), this is a credible, biology-driven alternative.
Standard of care?
Perhaps not universal—but choice matters in BRAF-mutant disease.
#BREAKWATER #BRAF #mCRC #ColorectalCancer #TargetedTherapy #Oncology
When cancer care demands
clarity, evidence, and precision —
Innovation must deliver answers.
Get ready for the next leap in precision
oncology.
#WherePrecisionMeetsDecision #CancerDiagnostics #NGSTesting #1CellAi
🧩Explore testing genetic alterations in #breastcancer with our recorded webinar — approved for 1.0 CMLE and 1.0 AMA PRA Category 1 credit. Learn more and register: https://t.co/obvCa5boBj #molpath #CancerResearch #NGSTesting
American Academy of Pediatrics Backs NGS Testing for Developmental Delay, Intellectual Disability. #PediatricGeneticTesting #NGStesting #WGS #WES #AmericanAcademyPediatrics #NeurodevelopmentalDisorders @GenomeWeb
https://t.co/8WVjhjXpbX
🔓 Unlock the unseen in BAL Diagnostics.
NeXGen NGS: Rapid, comprehensive fungal and AFB detection from blood and BAL. (Bronchoalveolar Lavage)
📄 READ the Organisms Dataset PDF:
https://t.co/OYd2GqP5AI
🎯 Precision diagnostics, redefined.
#ViracorNeXGenBAL #NGSTesting #Bronchoalveolar #FungalInfection
🧬 Learn about somatic NGS tumor testing in #breastcancer! Approved for 1.0 CMLE and AMA PRA Category 1 credit, this webinar covers predictive and tissue-agnostic markers and diagnostics. Register👉🏽https://t.co/gsxyvIfyfp #NGSTesting
📢 NEW ASSAY ALERT - Now Available!
READ 👉 https://t.co/rnNBd3oTw3
🔓 Unlock the unseen. NeXGen NGS: Rapid, comprehensive fungal & AFB detection from blood and BAL. 🎯 Precision diagnostics, redefined.
#ViracorNeXGen #NGSTesting #Bronchoalveolar #IDtwitter #Fungal #Candida
🌟 Day 1 at the Masters in Therapeutic Oncology Summit | MaTOS GU Edition 2025 🌟
Session 1 just wrapped up, and what an insightful start to the summit! 🙌 We had the privilege of interviewing Dr. Arnab Basu👨⚕️
#MaTOS2025 #OncologyExperts #NGSTesting @arnabguonc @EdgardoSantosMD
Is your clinical diagnostic lab experiencing rising sample volumes and shrinking turnaround times? 😩 On March 11, discover how the latest enhancements to QCI Interpret for Oncology can accelerate your clinical reporting workflows for #precisiononcology #NGStesting 🚀⬇️
<24H: Visit our @Labroots virtual booth to learn how to supercharge NGS testing for #oncology! Ft. expert-curated data and ultra-fast software 👇
Bonus: hear from the head of Serbia’s national cancer research center on cutting through the noise in #NGStesting. Don’t miss this!
🎧 Active noise canceling: what if I apply that to my data? 🤯
Tomorrow, hear how Serbia’s national #cancer research center uses expert-curated variant content to bypass the noise in their #NGStesting results, letting them streamline and focus on clinically relevant variants ⬇️
👋 We’re still at the @CG_Consortium #CGCAnnual2024 meeting in St. Louis, MO until tomorrow! Drop by booth 27 to explore our solutions for #oncology #NGStesting. Get free demos by just walking in, or schedule your personalized consult ⬇️
🤩 QIAGEN will be at the 15th @CG_Consortium meeting in St. Louis, MO, USA on Aug. 4–7! Listen to our talk on implementing comprehensive genomic profiling, or stop by booth 27 to learn how we can augment your pipeline for #NGStesting for #oncology. See you there 👇 #CGCAnnual2024
👨⚕️ Does your lab do #NGStesting for #oncology? We can help you increase test throughput & reduce turnaround times while delivering comprehensive, oncologist-ready reports that match patients to the most apt therapies & clinical trials. Interested? Join us tomorrow to learn how 👇
Experiencing diagnostic bottlenecks? 😓 Find out how you can perform better #NGStesting for #oncology, from scaling up to producing oncologist-ready reports within a shorter turnaround time, on July 18 (with multiple timeslots, so you don’t miss out 😉). Save your seat ⬇️
QIAGEN's Software QCI Interpret Accelerates Clinical Reporting Turnaround Time For High Throughput NGS Testing Labs
Single gene tests and small gene panels are being replaced with large.
Read More: https://t.co/MfXHjQuT8s
#ClinicalReporting #NGSTesting #HighThroughput
😫 Do you find NGS testing out of reach? Not anymore.
Now, even small and decentralized labs can adopt #NGStesting for #oncology and inherited diseases without extensive time and resource investment. Join our webinar to find out how ⬇️
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