AGTC Genomics

🔍 𝐃𝐞𝐭𝐞𝐜𝐭 𝐂𝐚𝐧𝐜𝐞𝐫 𝐄𝐚𝐫𝐥𝐲 𝐰𝐢𝐭𝐡 𝐂𝐚𝐧𝐜𝐞𝐫𝐒𝐜𝐫𝐞𝐞𝐧𝐃𝐱 𝐛𝐲 𝐀𝐆𝐓𝐂 𝐆𝐞𝐧𝐨𝐦𝐢𝐜𝐬 CancerScreenDx is revolutionizing early cancer detection! A single blood test can now identify over 110 types of cancer, giving you a proactive edge to fight cancer when it's most treatable. 🌟 𝐖𝐡𝐲 𝐂𝐚𝐧𝐜𝐞𝐫𝐒𝐜𝐫𝐞𝐞𝐧𝐃𝐱? ✔Comprehensive Detection: Screen for 110+ types of cancer, surpassing traditional methods. ✔Accurate & Predictive: Pinpoints cancer origin with precision for early intervention. ✔Non-Invasive: One simple blood draw for easy and accessible screening. Fast Turnaround: Results within 7–14 days from our ISO 15189-certified lab. 🧬 𝐇𝐨𝐰 𝐈𝐭 𝐖𝐨𝐫𝐤𝐬 CancerScreenDx detects circulating tumor DNA (ctDNA) in the blood, identifying cancer signals early and accurately predicting their source. This empowers patients and healthcare providers to take timely action with confidence. 🎯 𝐖𝐡𝐨 𝐒𝐡𝐨𝐮𝐥𝐝 𝐆𝐞𝐭 𝐓𝐞𝐬𝐭𝐞𝐝? ● Individuals aged 40+ for routine screening. ● Those with family history of cancer. ● People with previous cancer diagnoses seeking proactive monitoring. ● Anyone with symptoms such as unexplained weight loss, fatigue, or persistent pain. 🚀 𝐁𝐞𝐧𝐞𝐟𝐢𝐭𝐬 𝐨𝐟 𝐄𝐚𝐫𝐥𝐲 𝐃𝐞𝐭𝐞𝐜𝐭𝐢𝐨𝐧 ● Higher survival rates with timely treatment. ● Improved quality of life through reduced treatment burdens. ● Cost savings by avoiding advanced-stage treatments. 𝐎𝐫𝐝𝐞𝐫 𝐓𝐨𝐝𝐚𝐲 𝐚𝐧𝐝 𝐓𝐚𝐤𝐞 𝐂𝐨𝐧𝐭𝐫𝐨𝐥 𝐨𝐟 𝐘𝐨𝐮𝐫 𝐇𝐞𝐚𝐥𝐭𝐡! 1️⃣ Order the test through your healthcare provider. 2️⃣ Blood draw at your lab or clinic. 3️⃣ Receive your results in just 7-14 working days. For more information: 📧 info@agtcgenomics.com 🌐 www.agtcgenomics.com

🌟 𝐉𝐨𝐢𝐧 𝐮𝐬 𝐟𝐨𝐫 𝐚 𝐦𝐞𝐚𝐧𝐢𝐧𝐠𝐟𝐮𝐥 𝐬𝐞𝐬𝐬𝐢𝐨𝐧 𝐨𝐧 𝐂𝐚𝐧𝐜𝐞𝐫 𝐀𝐰𝐚𝐫𝐞𝐧𝐞𝐬𝐬 𝐭𝐡𝐢𝐬 𝐒𝐚𝐭𝐮𝐫𝐝𝐚𝐲, 𝐍𝐨𝐯𝐞𝐦𝐛𝐞𝐫 9𝐭𝐡, 𝐚𝐭 𝐀𝐦𝐞𝐞𝐧'𝐬 𝐂𝐚𝐟é, 𝐊𝐮𝐚𝐥𝐚 𝐋𝐮𝐦𝐩𝐮𝐫, 𝐟𝐫𝐨𝐦 9:30 𝐀𝐌 𝐭𝐨 1:00 𝐏𝐌. 🌟 At AGTC Genomics, we're dedicated to advancing cancer awareness and early detection. This event brings together esteemed experts, including Dr. Nur Fadhlina Abdul Satar, Dr. Lee Ah Keh, and our own Prof. Dr. Chee-Onn Leong, for insightful discussions on holistic cancer treatments and the power of early detection. 📅 Agenda Highlights: ● Medical talk on holistic cancer treatment ● Psychosocial care discussion with an oncologist ● Cutting-edge advancements in early cancer detection Let's continue the journey toward a future where lives are saved through early awareness and accessible diagnostics. 🔗 [Scan QR to RSVP] or reach out for more information. 📍 Location: Ameen's Café, Ground Floor, 39, Jalan Ampang, 50100 Kuala Lumpur 📞 Contact: 011-7251 4068 Together, let's make a difference. #CancerAwareness #AGTCGenomics #EarlyDetection #HolisticCare #CancerResearch #HealthcareCommunity

🚀 𝐔𝐧𝐥𝐨𝐜𝐤 30% 𝐎𝐟𝐟 𝐘𝐨𝐮𝐫 𝐍𝐞𝐱𝐭 𝐓𝐫𝐚𝐧𝐬𝐜𝐫𝐢𝐩𝐭𝐨𝐦𝐢𝐜𝐬 𝐒𝐞𝐪𝐮𝐞𝐧𝐜𝐢𝐧𝐠 𝐏𝐫𝐨𝐣𝐞𝐜𝐭! 🚀 𝘌𝘯𝘥 𝘵𝘩𝘦 𝘺𝘦𝘢𝘳 𝘴𝘵𝘳𝘰𝘯𝘨 𝘸𝘪𝘵𝘩 𝘦𝘹𝘤𝘭𝘶𝘴𝘪𝘷𝘦 𝘴𝘢𝘷𝘪𝘯𝘨𝘴 𝘰𝘯 𝘤𝘶𝘵𝘵𝘪𝘯𝘨-𝘦𝘥𝘨𝘦 𝘵𝘳𝘢𝘯𝘴𝘤𝘳𝘪𝘱𝘵𝘰𝘮𝘪𝘤𝘴 𝘴𝘰𝘭𝘶𝘵𝘪𝘰𝘯𝘴. 𝘚𝘶𝘱𝘦𝘳𝘤𝘩𝘢𝘳𝘨𝘦 𝘺𝘰𝘶𝘳 𝘳𝘦𝘴𝘦𝘢𝘳𝘤𝘩 𝘸𝘪𝘵𝘩 𝘵𝘩𝘪𝘴 𝘭𝘪𝘮𝘪𝘵𝘦𝘥-𝘵𝘪𝘮𝘦 𝘰𝘧𝘧𝘦𝘳 — 𝘢𝘷𝘢𝘪𝘭𝘢𝘣𝘭𝘦 𝘶𝘯𝘵𝘪𝘭 𝘋𝘦𝘤𝘦𝘮𝘣𝘦𝘳 30𝘵𝘩, 2024. 𝘋𝘰𝘯’𝘵 𝘮𝘪𝘴𝘴 𝘰𝘶𝘵! In genomics, capturing a complete view of gene expression is vital for accurate biological insights. But when it comes to RNA sequencing, two approaches often stand out: Whole-Transcriptome Sequencing (WTS) and mRNA Sequencing (RNA-seq). While both have unique strengths, there are key differences that make WTS invaluable in research and diagnostics. Let's dive in! 🔬 1️⃣ 𝐂𝐨𝐦𝐩𝐫𝐞𝐡𝐞𝐧𝐬𝐢𝐯𝐞 𝐂𝐨𝐯𝐞𝐫𝐚𝐠𝐞 𝐨𝐟 𝐭𝐡𝐞 𝐓𝐫𝐚𝐧𝐬𝐜𝐫𝐢𝐩𝐭𝐨𝐦𝐞 RNA-seq focuses specifically on mRNA, giving insights into protein-coding genes by analyzing exons. This is excellent for studying gene expression at the coding level. WTS, on the other hand, captures ALL RNA types—including non-coding RNA, long non-coding RNA (lncRNA), small RNA, microRNA (miRNA) and circular RNA. This gives a complete view of the transcriptome, unlocking data that RNA-seq can't access, which is essential for understanding complex regulatory networks. 2️⃣ 𝐍𝐨𝐧-𝐂𝐨𝐝𝐢𝐧𝐠 𝐑𝐍𝐀𝐬 𝐚𝐧𝐝 𝐓𝐡𝐞𝐢𝐫 𝐑𝐨𝐥𝐞 𝐢𝐧 𝐃𝐢𝐬𝐞𝐚𝐬𝐞 With the broader coverage of WTS, researchers can detect non-coding RNAs, which play crucial roles in gene regulation, disease mechanisms, and cancer pathways. These RNA species often remain underexplored with RNA-seq, limiting the depth of insights for diseases with regulatory complexity. 3️⃣ 𝐃𝐞𝐭𝐞𝐜𝐭𝐢𝐧𝐠 𝐆𝐞𝐧𝐞 𝐅𝐮𝐬𝐢𝐨𝐧𝐬 𝐚𝐧𝐝 𝐈𝐬𝐨𝐟𝐨𝐫𝐦𝐬 Unlike mRNA sequencing, WTS allows for the discovery of gene fusions, alternative splicing events, and transcript isoforms that contribute to cellular diversity. These details can be pivotal in cancer research, where fusion genes and isoform diversity often drive disease progression and drug resistance. 4️⃣ 𝐁𝐢𝐨𝐦𝐚𝐫𝐤𝐞𝐫 𝐃𝐢𝐬𝐜𝐨𝐯𝐞𝐫𝐲 𝐚𝐧𝐝 𝐃𝐢𝐚𝐠𝐧𝐨𝐬𝐭𝐢𝐜𝐬 𝐏𝐨𝐭𝐞𝐧𝐭𝐢𝐚𝐥 WTS’s ability to capture the entire RNA landscape opens doors to more comprehensive biomarker discovery. Non-coding RNAs, fusion genes, and novel transcripts offer new diagnostic markers that RNA-seq would miss, broadening potential applications in personalized medicine. In essence, while mRNA sequencing remains a powerful tool for understanding gene expression, Whole-Transcriptome Sequencing offers a 360-degree view that is unmatched. For researchers and clinicians aiming to unravel complex diseases, WTS provides the full transcriptomic picture needed to make breakthrough discoveries. 🌐💡 Let’s continue advancing our genomic toolbox and leverage these innovations to drive impactful insights!

November is the #LungCancer Awareness Month, and we're honored to support the lung cancer community in raising awareness and promoting education about this disease.

🧬 𝐌𝐨𝐧𝐢𝐭𝐨𝐫 𝐂𝐚𝐧𝐜𝐞𝐫 𝐑𝐞𝐜𝐮𝐫𝐫𝐞𝐧𝐜𝐞 𝐰𝐢𝐭𝐡 𝐂𝐨𝐧𝐟𝐢𝐝𝐞𝐧𝐜𝐞 – 𝐈𝐧𝐭𝐫𝐨𝐝𝐮𝐜𝐢𝐧𝐠 𝐂𝐚𝐧𝐜𝐞𝐫𝐓𝐑𝐀𝐂𝐄 𝐛𝐲 𝐀𝐆𝐓𝐂 𝐆𝐞𝐧𝐨𝐦𝐢𝐜𝐬 Cancer recurrence can be unpredictable, but with CancerTRACE, you gain the tools to stay ahead. Our non-invasive liquid biopsy detects minimal residual disease (MRD) through circulating tumor DNA (ctDNA) in the bloodstream—providing peace of mind and actionable insights. 🌟 𝐖𝐡𝐲 𝐂𝐚𝐧𝐜𝐞𝐫𝐓𝐑𝐀𝐂𝐄? ✔Non-Invasive: No need for surgery—just a simple blood draw. ✔Cost-Effective: More affordable and repeatable than traditional biopsies. ✔Fast & Reliable: Results within 7–14 working days from our ISO 15189-certified lab. ✔High Sensitivity: Detects even small amounts of cancer DNA for early intervention. 🚀 𝐊𝐞𝐲 𝐁𝐞𝐧𝐞𝐟𝐢𝐭𝐬 𝐨𝐟 𝐂𝐚𝐧𝐜𝐞𝐫𝐓𝐑𝐀𝐂𝐄 ● Early Detection: Identifies recurrence before symptoms appear. ● Early Detection: Dynamic Monitoring: Track real-time changes to adjust treatment plans. ● Early Detection: Wide Applicability: Effective across solid tumors and hematological cancers. ● Early Detection: Comprehensive Testing: Monitor 523 genes relevant to cancer recurrence. 🧬 𝐇𝐨𝐰 𝐭𝐨 𝐆𝐞𝐭 𝐒𝐭𝐚𝐫𝐭𝐞𝐝 1️⃣ Order the test through your healthcare provider. 2️⃣ Provide a blood sample at a clinic or lab. 3️⃣ Receive actionable insights to guide personalized care. With CancerTRACE, you’re empowered to make informed decisions and live with confidence—knowing your health is monitored with precision and care. 📧 info@agtcgenomics.com 🌐 www.agtcgenomics.com #CancerTRACE #LiquidBiopsy #CancerRecurrence #PrecisionMedicine #AGTCGenomics #MRD #HealthcareInnovation

🌟 𝐄𝐱𝐩𝐥𝐨𝐫𝐞 𝐎𝐮𝐫 𝐂𝐥𝐢𝐧𝐢𝐜𝐚𝐥 𝐆𝐞𝐧𝐨𝐦𝐢𝐜 𝐒𝐞𝐫𝐯𝐢𝐜𝐞𝐬 𝑵𝒐𝒗𝒂𝑫𝒙™ – 𝑪𝒍𝒊𝒏𝒊𝒄𝒂𝒍 𝑾𝒉𝒐𝒍𝒆 𝑮𝒆𝒏𝒐𝒎𝒆 𝑺𝒆𝒒𝒖𝒆𝒏𝒄𝒊𝒏𝒈 (𝑾𝑮𝑺) 🧬 Comprehensive genome coverage to diagnose complex and undiagnosed cases with certainty. 🔍 Recommended for rare diseases, family planning, and rapid diagnostics in NICU/PICU settings. 𝑰𝒏𝒔𝒊𝒈𝒉𝒕𝑫𝒙™ – 𝑪𝒍𝒊𝒏𝒊𝒄𝒂𝒍 𝑬𝒙𝒐𝒎𝒆 𝑺𝒆𝒒𝒖𝒆𝒏𝒄𝒊𝒏𝒈 (𝑾𝑬𝑺) 🧪 Focus on protein-coding regions to uncover disease-causing variants efficiently. 🧬 Ideal for diagnosing patients with atypical symptoms and genetic heterogeneity. 𝑯𝒐𝒓𝒊𝒛𝒐𝒏𝑫𝒙™ – 𝑪𝒐𝒎𝒑𝒓𝒆𝒉𝒆𝒏𝒔𝒊𝒗𝒆 𝑪𝒂𝒓𝒓𝒊𝒆𝒓 𝑺𝒄𝒓𝒆𝒆𝒏𝒊𝒏𝒈 👪 Detect carrier status to assess the risk of transmitting genetic conditions to offspring. 💡 Informed family planning through advanced screening. 𝑶𝒓𝒊𝒈𝒆𝒏𝑫𝒙™ – 𝑵𝒆𝒘𝒃𝒐𝒓𝒏 𝑮𝒆𝒏𝒆𝒕𝒊𝒄 𝑺𝒄𝒓𝒆𝒆𝒏𝒊𝒏𝒈 🍼 Early detection of 130+ inborn errors of metabolism for newborns and infants. 💊 Supports prompt interventions to improve health outcomes. 𝑶𝒅𝒚𝒔𝒔𝒆𝒚𝑫𝒙™ – 𝑹𝒂𝒓𝒆 𝑫𝒊𝒔𝒆𝒂𝒔𝒆 𝑺𝒐𝒍𝒖𝒕𝒊𝒐𝒏𝒔 🔎 Diagnose rare hereditary diseases with advanced genomic technology. 🧬 End long diagnostic journeys with definitive results. 𝑷𝒉𝒂𝒓𝒎𝑷𝑮𝒙™ – 𝑪𝒐𝒎𝒑𝒓𝒆𝒉𝒆𝒏𝒔𝒊𝒗𝒆 𝑷𝒉𝒂𝒓𝒎𝒂𝒄𝒐𝒈𝒆𝒏𝒐𝒎𝒊𝒄𝒔 𝑻𝒆𝒔𝒕 💊 Tailor medications based on genetic makeup to enhance drug efficacy and minimize side effects. 𝑪𝒐𝒏𝒕𝒊𝒏𝒖𝒖𝒎𝑫𝒙™ – 𝑷𝒆𝒓𝒔𝒐𝒏𝒂𝒍 𝑮𝒆𝒏𝒐𝒎𝒊𝒄𝒔 𝒂𝒏𝒅 𝑫𝒊𝒔𝒆𝒂𝒔𝒆 𝑹𝒊𝒔𝒌 𝑷𝒓𝒆𝒅𝒊𝒄𝒕𝒊𝒐𝒏 🔮 Polygenic risk scores to help individuals manage and mitigate potential health risks. 𝑯𝑳𝑨-𝑫𝒙™ – 𝑯𝑳𝑨 𝑻𝒚𝒑𝒊𝒏𝒈 𝒇𝒐𝒓 𝑶𝒓𝒈𝒂𝒏 𝑻𝒓𝒂𝒏𝒔𝒑𝒍𝒂𝒏𝒕 🧬 Ensure compatibility and reduce rejection risks with precise HLA matching and monitoring. 🚀 𝐖𝐡𝐲 𝐀𝐆𝐓𝐂 𝐆𝐞𝐧𝐨𝐦𝐢𝐜𝐬? ● World-Class Technology: Powered by the latest advancements in NGS and bioinformatics. ● Trusted Expertise: Supported by PhD scientists, pathologists, and genetic counselors. ● High Data Security: All testing is conducted locally in Malaysia, ensuring secure data handling. ● Fast Turnaround: Results within 7–14 days to accelerate patient care. 💡 Take the next step towards precision healthcare—empower your clinical decisions with the most comprehensive genomic services in the region. 📧 info@agtcgenomics.com 🌐 www.agtcgenomics.com #Genomics #PrecisionMedicine #PersonalizedHealthcare #ClinicalNGS #AGTCGenomics

🔬 𝐑𝐞𝐯𝐨𝐥𝐮𝐭𝐢𝐨𝐧𝐢𝐳𝐞 𝐂𝐚𝐧𝐜𝐞𝐫 𝐂𝐚𝐫𝐞 𝐰𝐢𝐭𝐡 𝐀𝐆𝐓𝐂 𝐆𝐞𝐧𝐨𝐦𝐢𝐜𝐬 𝐂𝐚𝐧𝐜𝐞𝐫 𝐒𝐨𝐥𝐮𝐭𝐢𝐨𝐧𝐬 Empower your clinical decisions with AGTC Genomics’ Cancer Genomics Solutions—designed to deliver precise, personalized cancer care and improve patient outcomes. 🌟 𝐎𝐮𝐫 𝐂𝐚𝐧𝐜𝐞𝐫 𝐆𝐞𝐧𝐨𝐦𝐢𝐜𝐬 𝐒𝐨𝐥𝐮𝐭𝐢𝐨𝐧𝐬 𝐚𝐭 𝐚 𝐆𝐥𝐚𝐧𝐜𝐞 𝐂𝐚𝐧𝐜𝐞𝐫𝐑𝐢𝐬𝐤𝐃𝐱: 𝐇𝐞𝐫𝐞𝐝𝐢𝐭𝐚𝐫𝐲 𝐂𝐚𝐧𝐜𝐞𝐫 𝐒𝐜𝐫𝐞𝐞𝐧𝐢𝐧𝐠 🔍 Detects mutations in 316 genes linked to 125 types of hereditary cancer. 🧬 Provides valuable insights for preventive action and family health management. 𝐂𝐚𝐧𝐜𝐞𝐫𝐒𝐜𝐫𝐞𝐞𝐧𝐃𝐱: 𝐌𝐮𝐥𝐭𝐢-𝐂𝐚𝐧𝐜𝐞𝐫 𝐄𝐚𝐫𝐥𝐲 𝐃𝐞𝐭𝐞𝐜𝐭𝐢𝐨𝐧 💉 Non-invasive blood test detecting 110+ types of cancer at their earliest stages. ⚡ Fast results and predictive analysis to support early interventions. 𝐏𝐫𝐞𝐜𝐢𝐬𝐞𝐃𝐱: 𝐂𝐨𝐦𝐩𝐫𝐞𝐡𝐞𝐧𝐬𝐢𝐯𝐞 𝐆𝐞𝐧𝐨𝐦𝐢𝐜 𝐏𝐫𝐨𝐟𝐢𝐥𝐢𝐧𝐠 🧪 Analyzes 523 genes to identify targeted therapies and immunotherapies. 🔄 Supports both pan-cancer profiling and cancer-specific diagnostics. 𝐋𝐢𝐪𝐮𝐢𝐝𝐃𝐱: 𝐜𝐭𝐃𝐍𝐀 𝐋𝐢𝐪𝐮𝐢𝐝 𝐁𝐢𝐨𝐩𝐬𝐲 💧 Monitors cancer in real time through a simple blood draw. 🎯 Detects genetic mutations to guide personalized therapy. 𝐂𝐚𝐧𝐜𝐞𝐫𝐓𝐑𝐀𝐂𝐄: 𝐂𝐚𝐧𝐜𝐞𝐫 𝐑𝐞𝐜𝐮𝐫𝐫𝐞𝐧𝐜𝐞 𝐌𝐨𝐧𝐢𝐭𝐨𝐫𝐢𝐧𝐠 📈 Tracks minimal residual disease (MRD) for early detection of recurrence. 🧬 Provides peace of mind with non-invasive monitoring tools. 🚀 𝐖𝐡𝐲 𝐀𝐆𝐓𝐂 𝐆𝐞𝐧𝐨𝐦𝐢𝐜𝐬? ✔Proven Accuracy: 99.9% accuracy with cutting-edge NGS technology. ✔ISO 15189-Certified Lab: Fast, reliable results in 7–14 working days. ✔End-to-End Data Security: All testing conducted locally in Malaysia. ✔Actionable Insights: Align with FDA-approved therapies and clinical trials. ✔Personalized Support: PhD experts available for consultation throughout your journey. 💡 Partner with AGTC Genomics to transform how cancer is diagnosed, treated, and monitored. Take control of your health with world-class genomic solutions. 📧 info@agtcgenomics.com 🌐 www.agtcgenomics.com #CancerGenomics #PrecisionMedicine #CancerCare #EarlyDetection #AGTCGenomics #PersonalizedTreatment

💧 𝐑𝐞𝐯𝐨𝐥𝐮𝐭𝐢𝐨𝐧𝐢𝐳𝐞 𝐂𝐚𝐧𝐜𝐞𝐫 𝐂𝐚𝐫𝐞 𝐰𝐢𝐭𝐡 𝐋𝐢𝐪𝐮𝐢𝐝𝐃𝐱 𝐜𝐭𝐃𝐍𝐀 𝐋𝐢𝐪𝐮𝐢𝐝 𝐁𝐢𝐨𝐩𝐬𝐲 𝐛𝐲 𝐀𝐆𝐓𝐂 𝐆𝐞𝐧𝐨𝐦𝐢𝐜𝐬 Say goodbye to invasive procedures! With LiquidDx, you can now monitor and detect cancer through a simple blood draw using circulating tumor DNA (ctDNA). 🌟 𝐖𝐡𝐲 𝐂𝐡𝐨𝐨𝐬𝐞 𝐋𝐢𝐪𝐮𝐢𝐝𝐃𝐱? ✔Non-Invasive: Just a blood draw—no surgery, no hospital admission. ✔Comprehensive: Profiles 523 genes and key genomic markers like TMB, MSI, and HRR. ✔Actionable Insights: Offers guidance on FDA-approved therapies and immunotherapies. ✔Fast Results: Delivered within 7–14 working days from our ISO 15189-certified lab. 🚀 𝐊𝐞𝐲 𝐁𝐞𝐧𝐞𝐟𝐢𝐭𝐬 𝐨𝐟 𝐋𝐢𝐪𝐮𝐢𝐝𝐃𝐱 ● Alternative to Tissue Biopsy: Ideal when a tissue sample is inaccessible or unavailable. ● Monitor Therapeutic Response: Track treatment effectiveness and detect residual disease early. ● Identify New Mutations: Stay ahead by detecting tumor heterogeneity and acquired resistance. ● Convenient & Reliable: Suitable for routine monitoring and optimizing personalized treatments. 🧬 𝐇𝐨𝐰 𝐭𝐨 𝐆𝐞𝐭 𝐒𝐭𝐚𝐫𝐭𝐞𝐝 1️⃣ Order the test with your healthcare provider. 2️⃣ Provide a blood sample—no complicated preparation needed. 3️⃣ Receive detailed genomic insights for targeted therapy or clinical trial options. 💡 LiquidDx gives patients and providers a non-invasive, fast, and precise alternative to traditional tissue biopsies, transforming cancer care and enabling precision medicine. 📧 info@agtcgenomics.com 🌐 www.agtcgenomics.com #LiquidBiopsy #PrecisionMedicine #ctDNA #AGTCGenomics #CancerCare #PersonalizedMedicine #HealthcareInnovation

𝐖𝐚𝐫𝐦 𝐃𝐞𝐞𝐩𝐚𝐯𝐚𝐥𝐢 𝐆𝐫𝐞𝐞𝐭𝐢𝐧𝐠𝐬 𝐟𝐫𝐨𝐦 𝐀𝐆𝐓𝐂 𝐆𝐞𝐧𝐨𝐦𝐢𝐜𝐬! Wishing you and your loved ones a joyous and bright Deepavali filled with happiness, prosperity, and new beginnings. May this festival of lights illuminate your life with hope and positivity. Happy Deepavali! Best wishes, The AGTC Genomics Team

🔬 𝐀𝐜𝐜𝐞𝐥𝐞𝐫𝐚𝐭𝐞 𝐃𝐢𝐬𝐜𝐨𝐯𝐞𝐫𝐲 𝐰𝐢𝐭𝐡 𝐀𝐆𝐓𝐂 𝐆𝐞𝐧𝐨𝐦𝐢𝐜𝐬 𝐒𝐞𝐫𝐯𝐢𝐜𝐞𝐬 At AGTC Genomics, we offer a wide range of genomics services designed to meet the most demanding research needs. Whether you're working on population genomics, oncology, agriculture, or personalized medicine, our cutting-edge technology and expertise ensure you get the insights you need—quickly and accurately. 🌟 𝐎𝐮𝐫 𝐂𝐨𝐦𝐩𝐫𝐞𝐡𝐞𝐧𝐬𝐢𝐯𝐞 𝐆𝐞𝐧𝐨𝐦𝐢𝐜𝐬 𝐒𝐞𝐫𝐯𝐢𝐜𝐞𝐬 ✔Whole Genome Sequencing (WGS): Explore the full genetic composition of an organism. ✔Whole Exome Sequencing (WES): Focus on coding regions to identify disease-causing mutations. ✔Single Cell Sequencing: Uncover cellular heterogeneity for immune and cancer research. ✔Metagenomic Sequencing: Understand complex microbial communities through 16S/18S or shotgun metagenomics. ✔Transcriptome Sequencing: Study gene expression and regulatory networks with RNA-Seq and mRNA analysis. ✔Epigenome Sequencing: Profile methylation patterns with WGBS and DNA methylation microarrays. 🚀 𝐖𝐡𝐲 𝐂𝐡𝐨𝐨𝐬𝐞 𝐀𝐆𝐓𝐂 𝐆𝐞𝐧𝐨𝐦𝐢𝐜𝐬? ● Competitive Pricing: Transparent, all-inclusive pricing models. ● Exceptional Data Quality: Over 90% of bases scoring Q30 or higher. ● Optimized Workflows: Efficient processes to ensure reliable results. ● Dedicated PhD Experts: Personalized support throughout the project. ● End-to-End Data Security: All services conducted in Malaysia, ensuring full data sovereignty. 🔧 𝐇𝐨𝐰 𝐈𝐭 𝐖𝐨𝐫𝐤𝐬 1️⃣ Send us your samples and project information. 2️⃣ Monitor progress with your dedicated project manager. 3️⃣ Receive ready-to-use results—aligned, analyzed, and secure BAM/VCF files. 💡 With AGTC Genomics, your data transforms into discovery. Our expert teams are ready to support you with state-of-the-art technology for any research project. 📧 info@agtcgenomics.com 🌐 www.agtcgenomics.com #Genomics #PrecisionMedicine #AGTCGenomics #NGS #GenomeSequencing #Transcriptomics #Epigenetics #ScientificResearch