The CGC represents clinical cytogeneticists, molecular geneticists, and molecular pathologists to promote best practices & education in clinical cancer genomics

United States
Joined August 2016
The CGC Early Career Webinar is almost here! Join the CGC Early Career Committee for The Negotiation Gene: Do You Have It? Featuring Kelly Quesnelle, PhD, FAAPE, and Avni B. Santani, PhD, FACMG 📅 October 28 | 10:00 AM PDT / 12:00 PM CDT / 1:00 PM EDT
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🌟 CGC Volunteer Spotlight: Fang Fang, PhD! Fang is a CGC Trainee Member, Assistant Laboratory Director at Natera, and a volunteer with the CCGA Working Group. We’re grateful for her contributions to the CGC community! 🧬 #CGC #CancerGenomics
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Tomorrow! Join Dr. David Scott as we dive into the evolving science of aggressive B-cell lymphoma. Explore molecular classifications and how they are advancing our understanding of the disease. 🗓️ October 13 | 12–1 p.m. ET Join the discussion: buff.ly/gw4QM8f
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Coming up Tuesday! Join CGC on October 13 for a scientific discussion with Dr. David Scott on molecular classifications of aggressive B-cell lymphoma and their implications for understanding the disease. 🗓️ Tuesday, October 13 ⏰ 12–1 p.m. ET
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A year of growth. A vision for 2027. Explore CGC’s 2026 highlights and priorities for the year ahead in a letter from President Cate Randal Paschal, PhD, FACMG. 👉 buff.ly/CfXT0lI #CancerGenomics #CGC
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🧬 Have an idea for CGC 2027? Invited Session Proposals are now open for the 18th Annual Meeting in Seattle! Submit ideas for scientific talks, panels, or interactive workshops. 📅 Deadline: November 16, 2026 Learn more and submit your proposal: buff.ly/CBfvBY6
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📚 New CGC publication! The Somatic Overgrowth & Vascular Anomalies Working Group published a review in Genetics in Medicine on genetic testing and mosaic variants. 🔗 Read the full article: buff.ly/jjbKBcq
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Q46: An 83-year-old man with DLBCL and a hx of prostate cancer has a TP53 path variant (VAF 45%) in blood. Family hx is negative. What’s the next step? A. Report + familial testing B. Report; likely de novo C. Test another tissue for mosaicism D. Test another tissue; likely CHIP
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Registration is open! The Negotiation Gene: Do You Have It? Learn practical strategies for negotiating salary, positions, resources, responsibilities & career opportunities with confidence. Featuring Kelly Quesnelle, PhD, FAAPE & Avni B. Santani, PhD, FACMG 📅 Oct. 28, 2026
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The CGC Early Career Initiative has had a busy year of webinars, mentoring, networking, and outreach for early-career professionals. Next up: 🧬 The Negotiation Gene: Do You Have It? 📅 Oct. 28, 2026 Register today 👉️ buff.ly/loo7fQj
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Registration is open! The Negotiation Gene: Do You Have It? Learn practical strategies for negotiating salary, roles, resources, responsibilities, and career opportunities with confidence. Featuring Kelly Quesnelle, PhD, FAAPE, & Avni B. Santani, PhD 📅 Oct. 28, 2026
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Q46: An 83-year-old man with DLBCL and a hx of prostate cancer has a TP53 path variant (VAF 45%) in blood. Family hx is negative.What’s the next step? A. Report + familial testing B. Report; likely de novo C. Test another tissue for mosaicism D. Test another tissue; likely CHIP
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Type your answer in the chat below and come back next week for the answer and explanation!
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Webinar reminder: Join us Oct. 13, 12–1 p.m. ET, for a scientific discussion on molecular classifications of aggressive B-cell lymphoma with David Scott, MD, PhD. Register: buff.ly/gw4QM8f
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Join us Oct. 13, 12–1 p.m. ET, for a scientific discussion on molecular classifications of aggressive B-cell lymphoma with David Scott, MD, PhD. 🧬 Register today: buff.ly/gw4QM8f
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Q.45 Fusion NGS missed a classic t(11;14) in mantle cell lymphoma. FISH found it at 90%. Why did NGS fail to detect it? A. FISH tested a different sample B. No IGH-CCND1 chimeric RNA was made C. Tumor content too low D. NGS tested the wrong sample
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