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Kepler Uniklinikum Harnesses SOPHiA GENETICS' Tech for Blood Cancer Diagnostics

Kepler Uniklinikum Harnesses SOPHiA GENETICS' Tech for Blood Cancer Diagnostics

开普勒医院利用SOPHiA GENETICS技术进行血液癌症诊断
Benzinga ·  06/13 06:06

SOPHiA GENETICS (NASDAQ:SOPH), a cloud-native healthcare technology company and a leader in data-driven medicine, today announced that Kepler Uniklinikum, Austria's second largest hospital, is live on SOPHiA GENETICS' platform. The hospital will use the SOPHiA DDM Platform to advance its next-generation sequencing (NGS) testing and diagnostics of blood-related cancers.

今天,SOPHiA遗传学公司(纳斯达克股票代码:SOPH),是一家云原生医疗科技公司,也是数据驱动型医学的领导者,宣布奥地利第二大医院Kepler Uniklinikum已经接入SOPHiA GENETICS的平台。该医院将使用SOPHiA DDM平台推进下一代测序(NGS)对血液相关癌症的检测和诊断。

Kepler Uniklinikum, which has 1,800 beds, is the central healthcare provider for Upper Austria. The hospital will implement the SOPHiA DDM Platform across its medical and chemical laboratory locations to deepen its in-house NGS testing capabilities and expand its offerings to its patients, specifically for those faced with blood cancers and disorders.

拥有1800张病床的Kepler Uniklinikum是上奥地利的中心医疗服务提供者。该医院将在其医疗和化学实验室中部署SOPHiA DDM平台,以深化其内部NGS测试能力,并将其服务扩展到其患者中,尤其是那些面临血液癌症和疾病的患者。

Cancer is the second most common cause of death in Austria, with about 42,000 people diagnosed with cancer each year.1 Additionally, on a global scale, blood cancers are the fifth most common type of cancer in the world.2 Advances in diagnostics and treatment of blood cancers depend on timely, cost-effective, and reliable sequencing data. The SOPHiA DDM Platform uses NGS to target key variants from FFPE, blood, or bone marrow samples, helping lead to fast and accurate detection of variants associated with the disease. The SOPHiA DDM Platform is specifically designed to compute a wide array of genomic variants and continually hones its machine learning algorithms to detect genomic variants associated with rare and challenging cases.

癌症是奥地利第二大死因,每年约有42,000人被诊断出患有癌症。此外,在全球范围内,血液癌症是世界上第五常见的癌症类型。血液癌症的诊断和治疗的进展取决于及时、具有成本效益和可靠的测序数据。SOPHiA DDM平台使用NGS来针对FFPE、血液或骨髓样本的关键变异,帮助快速准确地检测与疾病相关的变异。SOPHiA DDM平台特别设计用于计算各种基因组变异,并不断改进其机器学习算法,以检测与罕见病例相关的基因组变异。

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