GeneDx to Showcase Key Research and Innovation at the 2025 American College of Medical Genetics (ACMG) Annual Meeting
GeneDx to Showcase Key Research and Innovation at the 2025 American College of Medical Genetics (ACMG) Annual Meeting
Presentations to highlight how GeneDx is leveraging AI to drive both better patient care and scale
演示將強調GeneDx如何利用人工智能推動更好的患者醫療和規模化
GAITHERSBURG, Md.--(BUSINESS WIRE)--Mar. 13, 2025--GeneDx (Nasdaq: WGS), a leader in delivering improved health outcomes through genomic insights, announced today its scientific contributions will be presented at the 2025 American College of Medical Genetics and Genomics (ACMG) Annual Clinical Genetics Meeting. GeneDx will showcase its leadership in genomic research and innovation, driving the industry forward with three platform presentations and two poster presentations.
馬里蘭州蓋瑟斯堡--(商業新聞)--2025年3月13日--GeneDx(納斯達克:WGS),作爲通過基因組洞察改善健康結果的領導者,今天宣佈其科學貢獻將在2025年美國醫學遺傳學和基因組學年會(ACMG)上展示。GeneDx將展示其在基因組研究和創新方面的領導地位,通過三場平台演示和兩場海報展示推動行業發展。
GeneDx earned one of the limited spots available for an industry-specific platform presentation on its AI-powered gene ranker embedded in its interpretation platform to enhance the speed and efficiency of clinical analysis. Through the combination of GeneDx's industry leading proprietary dataset, publicly available data, and the power of AI, Multiscore prioritizes genes with positive findings in exome and genome sequences by ranking them based on alignment with a patient's clinical presentation. GeneDx's AI-powered gene ranker accelerates analysis, reducing turnaround times and costs for patients and ultimately increasing access to care.
GeneDx獲得了針對其嵌入解釋平台的人工智能驅動基因評估器進行行業特定平台演示的有限席位,以提高臨牀分析的速度和效率。通過GeneDx領先的專有數據集、公開可用數據和人工智能的結合,Multiscore根據與患者臨牀表現的匹配程度,對外顯子和基因組序列中具有正面發現的基因進行優先排序。GeneDx的人工智能驅動基因評估器加快了分析過程,減少了患者的週轉時間和成本,最終增加了醫療保健的可及性。
- Multiscore, a Gene Ranker Powered by Artificial Intelligence and Real-World Clinical Data, Shows High Sensitivity in 10,000 Exomes and Genomes will be presented by Vinnie Ustach, PhD (GeneDx) on Thursday, March 20, 2025 at 12:00 pm PT in Meeting Room: Petree Hall D
- 由Vinnie Ustach博士(GeneDx)於2025年3月20日週四中午12:00(太平洋時間)在會議室:Petree Hall D介紹的Multiscore,一種基於人工智能和真實世界臨牀數據的基因評估器,在10,000個外顯子和基因組中顯示出高靈敏度
Featured as a Top 20 Poster, GeneDx will also present findings from an RNA sequencing program used to aid in variant of uncertain significance (VUS) resolution for patients that received exome-based testing for rare disease.
作爲前20名海報之一,GeneDx還將展示用於幫助解決不確定意義(VUS)變異的RNA測序項目的研究結果,這些患者接受了針對罕見疾病的外顯子測試。
- Clinical Impact of RNA Sequencing on VUS Resolution in a Diverse Rare Disease Cohort of Over 100,000 Patients will be presented by Melanie Napier, MSc, MSc, CGC, CCGC (GeneDx) on Thursday, March 20 at 12:00 pm PT in the Exhibit Hall Learning Lounge and Friday, March 21 at 10:30 am PT at West Exhibit Hall A
- RNA測序對超過100,000名患者的VUS解決的臨牀影響將由Melanie Napier碩士(GeneDx)於2025年3月20日(週四)中午12:00(太平洋時間)在展覽廳學習休息區及2025年3月21日(週五)上午10:30(太平洋時間)在西展覽廳A進行介紹。
"GeneDx's research, collaborations and AI-powered innovations being presented at ACMG reflect our commitment to advancing the utilization of exome and genome testing to improve patient care," said Dr. Paul Kruszka, MD, FACMG, Chief Medical Officer at GeneDx. "By investing in industry-changing research and harnessing cutting-edge technology, we are enhancing the speed, accuracy, and impact of genetic insights, ultimately enabling a precise diagnosis, faster and better outcomes for patients, and also driving cost efficiency."
"GeneDx的研究、合作以及人工智能驅動的創新在ACMG上展示了我們致力於推進外顯子和基因組測試的應用,以改善病人護理的承諾," GeneDx的首席醫療官Paul Kruszka博士說道。"通過投資於改變行業的研究,並利用尖端技術,我們正在提升基因洞察的速度、準確性和影響力,最終實現精確診斷,爲病人帶來更快更好的結果,同時推動成本效率。"
GeneDx leverages its industry-leading dataset, exome and genome across numerous studies to advance clinical care for pediatric patients and showcase strong evidence to expand utilization. Through strategic collaborations with PacBio, GUARDIAN, and Seqfirst, GeneDx champions research to drive forward exome and genome sequencing as the standard of care in diverse clinical settings.
GeneDx利用其行業領先的數據集,針對衆多研究中的外顯子和基因組,促進兒科患者的臨牀護理,並展示強有力的證據以擴大應用。通過與PacBio、GUARDIAN和Seqfirst的戰略合作,GeneDx積極推動研究,以推進外顯子和基因組測序作爲不同臨牀環境中的標準護理。
GeneDx collaborated on the following posters and presentations:
GeneDx在以下海報和演示中進行了合作:
- Resolution of large complex VNTRs with HiFi sequencing: applications in LPA Kringle IV-type 2 repeat and D4Z4 repeat will be presented by Xiao Chen, PhD on Thursday, March 20 at 12:00 pm PT in Meeting Room: Petree Hall D
- GUARDIAN Expanded Newborn Screening Study: Early Experiences will be presented by Brenna Boyd, MS, CGC on Friday, March 21 at 1:30 pm PT in Meeting Room: 501 ABC
- Parental needs during pediatric whole genome sequencing for developmental disorders: an interview study will be presented by Priyanka Murali, MS, CGC on Thursday, March 20 at 10:30 am PT in West Exhibit Hall A
- 利用HiFi測序解決大型複雜VNTR:在LPA Kringle IV型2重複和D4Z4重複中的應用將由Chen Xiao博士在3月20日星期四下午12:00(太平洋時間)在會議室:Petree Hall D進行展示。
- GUARDIAN擴展新生兒篩查研究:早期經驗將由Brenna Boyd,MS,CGC於3月21日星期五下午1:30(太平洋時間)在會議室:501 農業銀行進行展示。
- 在發展性疾病的兒科全基因組測序中,父母的需求:一項訪談研究將由Priyanka Murali,MS,CGC於3月20日星期四上午10:30(太平洋時間)在西展覽廳A進行展示。
About GeneDx:
At GeneDx (Nasdaq: WGS), we believe that everyone deserves personalized, targeted medical care—and that it all begins with a genetic diagnosis. Fueled by one of the world's largest, rare disease data sets, our industry-leading exome and genome tests translate complex genomic data into clinical answers that unlock personalized health plans, accelerate drug discovery, and improve health system efficiencies. For more information, please visit genedx.com and connect with us on LinkedIn, Facebook, and Instagram.
關於GeneDx:
在GeneDx(納斯達克:WGS),我們相信每個人都應得到個性化、針對性的醫療保健——而這一切都始於遺傳診斷。依託世界上最大的罕見疾病數據集之一,我們行業領先的外顯子和基因組檢測將複雜的基因組數據轉化爲臨牀解答,解鎖個性化健康計劃,加速藥物發現,提高健康系統效率。有關更多信息,請訪問genedx.com,並在LinkedIn、Facebook和Instagram上與我們聯繫。
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Source: GeneDx
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