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Clinical research blog

Explore our blog for insights into the big questions in precision medicine and clinical research.

Podcast recap: Balancing privacy and progress in healthcare data with Ben Goldacre

In the latest episode of The Genetics Podcast, Sano CEO Patrick Short had an enlightening conversation with Ben Goldacre, a prominent figure in healthcare data ...
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Healthcare policy frameworks supporting precision medicine

Establishing robust policy frameworks to support precision medicine involves creating an ecosystem that fosters innovation, ensures safety and efficacy, and pro...
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Implementing genomics: Key strategies for early detection in at-risk populations

To fully harness the potential of genomics for early detection and prevention in at-risk populations, a comprehensive and strategic approach is crucial. Below, ...
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Exploring the future of genomics in healthcare: Early detection and prevention strategies for at-risk populations

Genomics has come a long way since the first human genome was sequenced in 2003. Today, sequencing a genome is not only faster but also significantly more affor...
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The Genetics Podcast recap: Championing diversity and accessibility in genomics with Mavis Machirori

In the latest episode of the Genetics Podcast, Sano CEO Patrick Short had the pleasure of speaking with Mavis Machirori, a senior researcher at the Ada Lovelace...
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Legal landscapes in precision medicine: Market access and intellectual property law

Precision medicine takes into account individual differences in patients' genes, environments, and lifestyles to guide treatment and prevention. That reliance o...
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Personalized medicine: Privacy, consent, and compliance

Personalized medicine depends on the characterization of individuals' phenotypes and genotypes, including molecular profiling, medical imaging, and lifestyle da...
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Genetic screening for prevention: Benefits and barriers

Many hereditary diseases are clinically manageable when detected early, yet most carriers are identified only after symptoms appear. Population genomic screenin...
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Newborn screening equity: Sequencing and global gaps

Over the last two decades, following the landmark achievement of sequencing the first complete human genome, a suite of powerful genetic tools has emerged. Gene...
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Prenatal genetic testing: NIPT, ethics, and newborn care

Genomic screening is changing how clinicians and families approach prenatal and neonatal care. These tests, which analyze fetal or newborn DNA for chromosomal c...
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