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This episode is brought to you by The Daily Quote, a podcast designed to kickstart your day in a positive way. Link is in the show notes.
Today we're diving into breakthroughs in medical care speed, AI decoding life, and global conservation wins. What if doctors could get life-saving genetic diagnoses for critically ill babies in just a few hours? That's our lead story. Plus, supercomputers deciphering the language of proteins, and new blood tests that can spot over 50 types of cancer.
First up: The New World Record for Fastest Human Whole Genome Sequencing.
Medicine is entering a new era of speed, and it's saving tiny lives. Boston Children's Hospital, working with Broad Clinical Labs and Roche Sequencing Solutions, has set a Guinness World Record for the fastest human whole genome sequencing. And this isn't just a fun record—it's a massive clinical breakthrough.
The team successfully sequenced and analyzed human samples, with the fastest taking less than four hours to provide data on genetic variants from extracted DNA.
Why is this huge? Currently, rapid genomic sequencing can take days, but many critical care decisions in the NICU need to happen in a matter of hours.
According to Dr. Monica Wojcik, this workflow means they could potentially send out a genome sequencing sample from a baby in the morning and have the diagnosis and report that same afternoon. In the NICU, a few hours could mean the difference between unnecessary procedures and targeted, life-saving treatment.
This breakthrough brings us one step closer to integrating point-of-care genome sequencing into standard critical care.
Now, let's talk about artificial intelligence and its war on disease. We have two incredible stories here, both centered on detection and decoding.
First: an AI-powered supercomputer is decoding the language of proteins.
Scientists at the University of Glasgow used the Tursa supercomputer—an advanced machine normally reserved for cosmic research—to create a protein language model called PLM-Interact.
Here's why this matters: proteins are the workhorses of life, essential to cellular structure and all biological processes. Their interactions are crucial, and disruptions in these protein-to-protein interactions often signal the start of diseases like cancer and genetic disorders. Viruses even exploit them to replicate.
And speaking of crucial detection, let's look at two major advances in cancer identification.
Google showcased DeepSomatic AI, a tool that accurately identifies cancer-causing genetic mutations. DeepSomatic achieved approximately 98% accuracy on a key benchmark.
Meanwhile, a massive trial shows great promise for the Galleri blood test, which can detect fragments of cancerous DNA circulating in the blood. Results from a North American trial involving 25,000 adults showed that the Galleri test identified a wide range of cancers.
Here's what's crucial: three-quarters of the cancers detected were types that currently have no screening program—like ovarian, liver, stomach, bladder, and pancreatic cancer. More than half the cancers were detected at an early stage, when successful treatment or cure is most likely. The test also correctly ruled out cancer in over 99% of those who tested negative.
Researchers believe this could fundamentally change the approach to cancer screening.
All right, let's dive into the speed round for even more great news from around the world.
Until next time, keep looking for the good in the world—because it's not only there, it's everywhere.
By Andrew McGivernThis episode is brought to you by The Daily Quote, a podcast designed to kickstart your day in a positive way. Link is in the show notes.
Today we're diving into breakthroughs in medical care speed, AI decoding life, and global conservation wins. What if doctors could get life-saving genetic diagnoses for critically ill babies in just a few hours? That's our lead story. Plus, supercomputers deciphering the language of proteins, and new blood tests that can spot over 50 types of cancer.
First up: The New World Record for Fastest Human Whole Genome Sequencing.
Medicine is entering a new era of speed, and it's saving tiny lives. Boston Children's Hospital, working with Broad Clinical Labs and Roche Sequencing Solutions, has set a Guinness World Record for the fastest human whole genome sequencing. And this isn't just a fun record—it's a massive clinical breakthrough.
The team successfully sequenced and analyzed human samples, with the fastest taking less than four hours to provide data on genetic variants from extracted DNA.
Why is this huge? Currently, rapid genomic sequencing can take days, but many critical care decisions in the NICU need to happen in a matter of hours.
According to Dr. Monica Wojcik, this workflow means they could potentially send out a genome sequencing sample from a baby in the morning and have the diagnosis and report that same afternoon. In the NICU, a few hours could mean the difference between unnecessary procedures and targeted, life-saving treatment.
This breakthrough brings us one step closer to integrating point-of-care genome sequencing into standard critical care.
Now, let's talk about artificial intelligence and its war on disease. We have two incredible stories here, both centered on detection and decoding.
First: an AI-powered supercomputer is decoding the language of proteins.
Scientists at the University of Glasgow used the Tursa supercomputer—an advanced machine normally reserved for cosmic research—to create a protein language model called PLM-Interact.
Here's why this matters: proteins are the workhorses of life, essential to cellular structure and all biological processes. Their interactions are crucial, and disruptions in these protein-to-protein interactions often signal the start of diseases like cancer and genetic disorders. Viruses even exploit them to replicate.
And speaking of crucial detection, let's look at two major advances in cancer identification.
Google showcased DeepSomatic AI, a tool that accurately identifies cancer-causing genetic mutations. DeepSomatic achieved approximately 98% accuracy on a key benchmark.
Meanwhile, a massive trial shows great promise for the Galleri blood test, which can detect fragments of cancerous DNA circulating in the blood. Results from a North American trial involving 25,000 adults showed that the Galleri test identified a wide range of cancers.
Here's what's crucial: three-quarters of the cancers detected were types that currently have no screening program—like ovarian, liver, stomach, bladder, and pancreatic cancer. More than half the cancers were detected at an early stage, when successful treatment or cure is most likely. The test also correctly ruled out cancer in over 99% of those who tested negative.
Researchers believe this could fundamentally change the approach to cancer screening.
All right, let's dive into the speed round for even more great news from around the world.
Until next time, keep looking for the good in the world—because it's not only there, it's everywhere.