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Kepler Uniklinikum Harnesses SOPHiA GENETICS' Tech for Blood Cancer Diagnostics

Kepler Uniklinikum Harnesses SOPHiA GENETICS' Tech for Blood Cancer Diagnostics

開普勒醫院利用SOPHiA GENETICS技術進行血液癌症診斷
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遺傳學公司(納斯達克股票代碼:SOPH),是一家雲原生醫療科技公司,也是數據驅動型醫學的領導者,宣佈奧地利第二大醫院Kepler Uniklinikum已經接入SOPHiA GENETICS的平台。該醫院將使用SOPHiA DDM平台推進下一代測序(NGS)對血液相關癌症的檢測和診斷。

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.

擁有1800張病牀的Kepler Uniklinikum是上奧地利的中心醫療服務提供者。該醫院將在其醫療和化學實驗室中部署SOPHiA DDM平台,以深化其內部NGS測試能力,並將其服務擴展到其患者中,尤其是那些面臨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.

癌症是奧地利第二大死因,每年約有42,000人被診斷出癌症。此外,在全球範圍內,血液癌是世界上第五種最常見的癌症類型。血液癌的診斷和治療的進展依賴於及時、經濟、可靠的測序數據。SOPHiA DDm平台使用NGS針對FFPE、血液或骨髓樣本的關鍵變異,有助於快速準確地檢測與該疾病相關的變異。SOPHiA DDm平台專門設計用於計算各種基因組變異,並不斷完善其機器學習算法,以檢測與罕見和具有挑戰性的案例相關的基因組變異。

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