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Laboratorio Barnafi-Krause is Live on SOPHiA DDM™

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SOPHiA GENETICS partners with Laboratorio Barnafi-Krause in Chile to enhance research capabilities for blood disorders, particularly Chronic Lymphocytic Leukemia (CLL), using advanced AI-powered technology. This collaboration aims to revolutionize diagnostic approaches and treatment strategies for leukemia patients in Chile and Latin America.
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The Chile-based Laboratory is using SOPHiA GENETICS' platform to advance its research capabilities with blood disorders

BOSTON and ROLLE, Switzerland, April 2, 2024 /PRNewswire/ -- SOPHiA GENETICS (Nasdaq: SOPH), a cloud-native software company and a leader in data-driven medicine, today announced that Laboratorio Barnafi-Krause is live on the SOPHiA DDM™ Platform. Laboratorio Barnafi-Krause, located in Chile, has implemented SOPHiA GENETICS' technology to help elevate its testing and analysis of blood cancers and diseases, including Leukemia.

Chronic Lymphocytic Leukemia (CLL) is a complex and critical condition, that accounts for 25–30 percent of all the leukemia in Western Countries, with over 100,000 incidence cases and over 40,000 death cases globally reported in 2019.1 With the implementation of SOPHiA GENETICS' technology, Laboratorio Barnafi-Krause is the exclusive laboratory in Chile equipped to conduct next-generation sequencing (NGS) for CLL.

"We take great pride in being at the forefront of genomic innovation and collaborating with SOPHiA GENETICS to drive progress in the diagnosis of leukemia helps us do just that," said Esteban Barnafi, Production Manager, and Technical Director of Laboratorio Barnafi-Krause. "As the sole laboratory in Chile with access to these specialized panels, we reaffirm our commitment to delivering cutting-edge healthcare solutions to our community, and ultimately aim to reshape the landscape of genomic medicine and improve outcomes for patients in the battle against leukemia."

This new capability, made possible by SOPHiA GENETICS and its advanced, AI-powered solution, underscores the collaborative initiatives aimed at refining diagnostic approaches and treatment strategies for leukemia patients in Chile.  With the SOPHiA DDM™ Platform, Laboratorio Barnafi-Krause will offer tailored NGS-based workflows that enable accurate and sensitive characterization of the complex mutational landscape associated with blood disorders. SOPHiA DDM™ provides high-quality, reproducible data and streamlined insights on up-to-date gene panels in a matter of days, helping to expedite and advance research and support clinicians in making data-driven recommendations for patients.

"The adoption of our technology from Laboratorio Barnafi-Krause demonstrates its ongoing commitment to progress the use of data-driven medicine throughout Chile and Latin America," said Ricardo Mendonca Filho, PhD., Managing Director, LAPAC, SOPHiA GENETICS. "The impact of this collaboration transcends geographical boundaries and will not only contribute to the overall healthcare in Chile, but also foster additional global collective intelligence on blood disorders."

Through the use of the SOPHiA DDM™ Platform, Laboratorio Barnafi-Krause will move forward in its work to reshape the landscape of genomic medicine in Chile and improve outcomes for patients in the battle against leukemia.

For more information on SOPHiA GENETICS, visit SOPHiAGENETICS.COM, or connect on X, LinkedInFacebook, and Instagram

About SOPHiA GENETICS 
SOPHiA GENETICS (Nasdaq: SOPH) is a software company dedicated to establishing the practice of data-driven medicine as the standard of care and for life sciences research. It is the creator of the SOPHiA DDM™ Platform, a cloud-native platform capable of analyzing data and generating insights from complex multimodal data sets and different diagnostic modalities. The SOPHiA DDM™ Platform and related solutions, products and services are currently used by a broad network of hospital, laboratory, and biopharma institutions globally. For more information, visit SOPHiAGENETICS.COM, or connect on X, LinkedInFacebook, and Instagram. Where others see data, we see answers. 

SOPHiA GENETICS products are for Research Use Only and not for use in diagnostic procedures unless specified otherwise. The information in this press release is about products that may or may not be available in different countries and, if applicable, may or may not have received approval or market clearance by a governmental regulatory body for different indications for use. Please contact support@sophiagenetics.com to obtain the appropriate product information for your country of residence.

SOPHiA GENETICS Forward-Looking Statements:
This press release contains statements that constitute forward-looking statements. All statements other than statements of historical facts contained in this press release, including statements regarding our future results of operations and financial position, business strategy, products, and technology, as well as plans and objectives of management for future operations, are forward-looking statements. Forward-looking statements are based on our management's beliefs and assumptions and on information currently available to our management. Such statements are subject to risks and uncertainties, and actual results may differ materially from those expressed or implied in the forward-looking statements due to various factors, including those described in our filings with the U.S. Securities and Exchange Commission. No assurance can be given that such future results will be achieved. Such forward-looking statements contained in this press release speak only as of the date hereof. We expressly disclaim any obligation or undertaking to update these forward-looking statements contained in this press release to reflect any change in our expectations or any change in events, conditions, or circumstances on which such statements are based, unless required to do so by applicable law. No representations or warranties (expressed or implied) are made about the accuracy of any such forward-looking statements.

1 https://biomedical-engineering-online.biomedcentral.com/articles/10.1186/s12938-021-00973-6

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SOURCE SOPHiA GENETICS

The partnership aims to advance research capabilities for blood disorders, specifically Chronic Lymphocytic Leukemia (CLL), using AI-powered technology.

CLL accounts for 25–30% of all leukemia cases in Western Countries, with over 100,000 incidence cases and over 40,000 death cases globally reported in 2019.

Laboratorio Barnafi-Krause is implementing SOPHiA GENETICS' technology for next-generation sequencing (NGS) for CLL.

Esteban Barnafi is the Production Manager and Technical Director of Laboratorio Barnafi-Krause, collaborating with SOPHiA GENETICS to drive progress in leukemia diagnosis.

The SOPHiA DDM™ Platform will offer tailored NGS-based workflows for accurate characterization of mutational landscape associated with blood disorders, providing high-quality data and insights in a matter of days.

The collaboration aims to reshape the landscape of genomic medicine in Chile and improve outcomes for leukemia patients through data-driven approaches.
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About SOPH

sophia genetics, world's largest clinical genomics community, brings together expertise in genetics, bioinformatics, machine learning and genomic privacy. based in switzerland, we are known for our high medical standards and swiss precision. sophia genetics offers health professionals who perform clinical genetic testing unparalleled bioinformatics analysis, quality assurance and secure banking of patient dna sequence data generated by ngs. the company helps clinical laboratories to reduce costs, overcome complexity, significantly improve the turnaround time for routine diagnosis and meet quality requirements related to the use of ngs in the clinic. our solution, the sophia ddm™ platform allows hospitals to better and faster diagnose patients using cutting edge ngs analytics algorithms and through knowledge sharing within the largest clinical genomics community in the world (+100 hospitals). the name « sophia » means wisdom in greek and it is the definition of our excellence based