Hereditary cancer testing has changed over the years as our understanding of genes grows and evolves. Explore what's next as Dr. Elizabeth Chao explains why pan-cancer panels are the future of genetic risk assessment. #AmbryKnowsGenes #genetictesting #hereditarycancer #SettingtheStandard https://hubs.ly/Q02YLYGc0
Ambry Genetics
生物技术研究
Aliso Viejo，CA 75,659 位关注者
Finding Answers Through Quality Genetic Testing
关于我们
Ambry Genetics is a company built by scientists, genetic counselors and physicians, dedicated to leading the clinical genomic diagnostic industry. Ambry boasts the largest genetic sequencing lab in the world; is CAP-accredited, CLIA-licensed and, as part of the Konica Minolta family, has access to the most complete suite of diagnostic technology in the world. Ambry Genetics' scope of clients includes some of the world's most respected academic institutions, pharmaceutical companies and leading treatment hospitals. Our experience, technology and dedication to science make us a trusted source for all clinical genetic testing, and an ideal partner for developing precision medicine solutions. Patients are at the core of everything we do, which is why Ambry partners with several non-profit organizations so that we can help both patients and clinicians alike find answers. Hiring Fraud Alert: Ambry/REALM IDx has received reports of employment scams in recent months that seek financial commitments, or requests personal information from job candidates. Unsuspecting job seekers have reported receiving unsolicited contacts by phone, email or text from individual(s) posing to be or represent Ambry/REALM IDx recruiter(s). If you’ve experienced either of these scenarios, please visit this page to learn more about hiring fraud: https://consumer.ftc.gov/articles/job-scams. Or visit https://realmidx.com/careers/recruitment-fraud-alert/ to learn more about our policy on recruitment fraud. You can confirm the legitimacy of a job posting by viewing our current open roles at https://realmidx.com/careers/.
- 网站
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https://www.ambrygen.com
Ambry Genetics的外部链接
- 所属行业
- 生物技术研究
- 规模
- 501-1,000 人
- 总部
- Aliso Viejo，CA
- 类型
- 私人持股
- 创立
- 1999
- 领域
- Molecular Diagnostic Testing、Clinical Diagnostic Exome、Breast Cancer Genetics、Hereditary Cancer、Cardio Genetics、Neuro Genetics、General Genetics、Family History Questionnaire、Pedigree Drawing Tool和Risk Assessment Tool
地点
Ambry Genetics员工
动态
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Check out this GenomeWeb article highlighting recent research on reduced penetrance pathogenic variants in the BRCA1/2 genes, published in npj Precision Oncology. Ambry was proud to collaborate on this study, which may help redefine how clinicians approach hereditary cancer risk counseling and management, as not all BRCA variants confer the same level of risk. https://hubs.ly/Q02YVGGn0
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Do you have questions about ExomeReveal?? Join us for a webinar Wednesday, December 11, to discover the power of adding RNA analysis to exome testing. Register today! https://hubs.ly/Q02YBcBF0 https://hubs.ly/Q02YB3Qy0
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Happy 25th Anniversary, Ambry! Ambry CEO Tom Schoenherr has a special thank-you message for everyone who helped us get to this day. #Ambry25 #ExperienceMatters #SettingtheStandard
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It's time to bust another #exome myth!
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This November, we reflect on the impact of hereditary pancreatic cancer on individuals and their loved ones. How to take action: Know Your Family History: Discuss any family instances of pancreatic cancer and other cancers (e.g., breast, colon) with your healthcare provider. Hereditary pancreatic cancer makes up ~10% of cases and can bring immense challenges to those at risk. Genetic Testing: If you have a strong family history of cancer, you can identify risks through genetic testing. Our enhanced CancerNext-Expanded panel includes guideline-based genes associated with inherited pancreatic cancer (as well as other cancers, like breast, colorectal, etc.), plus offers an optional 5-gene panel add-on for pancreatitis. https://hubs.ly/Q02Y4kJ80 Spread Awareness: By sharing knowledge and personal stories, we can foster a supportive community that empowers those affected by this disease. Together, we can make a difference. Early detection saves lives! #PancreaticCancer #HereditaryCancer #GeneticTesting #Awareness
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Only ~4% of individuals at risk due to family or personal history undergo genetic counseling or genetic testing. The Ambry CARE Program?? is working to change that by empowering healthcare providers with tools to identify more at-risk patients and connect them with education, testing, and counseling. https://hubs.ly/Q02XhkfJ0
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Join us in Texas this December for the San Antonio Breast Cancer Symposium. Ambry is dedicated to guideline-based screening and genetic testing for the prevention, early detection and informed treatment of breast cancer. We have been #SettingtheStandard in #genetictesting for 25 years. We hope to see you at booth 1052 to discuss our enhanced hereditary cancer test menu and The Ambry CARE Program?.
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Myth 2: Exome testing returns a higher rate of variants of uncertain significance (VUS) compared to multigene panels. Answer: False! In a Genetics in Medicine publication from 2023, Rehm et al concluded that the VUS rate in exome and genome testing were actually 10% lower on average compared to multigene panels. Those differences grew as panel size increased. Read more: https://hubs.ly/Q02Y4-GS0
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