Name:
Whole-genome sequencing for precision medicine
Description:
Whole-genome sequencing for precision medicine
Thumbnail URL:
https://cadmoremediastorage.blob.core.windows.net/6a3cdce3-bf67-438d-b59a-a5441a0ad152/videoscrubberimages/Scrubber_0.jpg
Duration:
T00H02M01S
Embed URL:
https://stream.cadmore.media/player/6a3cdce3-bf67-438d-b59a-a5441a0ad152
Content URL:
https://cadmoreoriginalmedia.blob.core.windows.net/6a3cdce3-bf67-438d-b59a-a5441a0ad152/Precision Medicine Btn Infocus - V2-1.m4v?sv=2019-02-02&sr=c&sig=2BS3r3N%2FXaXodlVTQ2QD0yDLU1D7sJPCdoOfzoQhloo%3D&st=2024-11-21T17%3A31%3A50Z&se=2024-11-21T19%3A36%3A50Z&sp=r
Upload Date:
2021-07-29T00:00:00.0000000
Transcript:
Language: EN.
Segment:0 .
[MUSIC PLAYING]
SPEAKER: Human whole genome sequencing has end to end applications from academic research to clinical practice. In fact, comprehensive genome analysis has been used across a range of scientific purposes. As the technology continues to advance, researchers have been able to better identify inherited disorders, characterize mutations for improved diagnosis and treatment of cancer, and predict adverse responses to drugs and treatments.
SPEAKER: From precision diagnostics to clinical trial development, hospitals and clinics are seeking to both understand a patient's risk for disease and how they respond to new drugs and treatment protocols. In fact, the whole genome sequencing technology that makes this possible is becoming routine and is no longer out of reach in terms of cost, speed, or the utility of captured data. Today, precision or personalized medicine is taking a front seat in areas like rare disease and oncology research.
SPEAKER: For example, one of the biggest challenges in rare diseases is getting a diagnosis. As whole genome sequencing advances, undiagnosed or misdiagnosed patients have been able to understand the cause of their symptoms, often identifying treatments and other life-improving therapies. Similarly, understanding the specific genetic variant associated with the patient's tumor is improving treatments, life expectancy, and quality of life by leaps and bounds.
SPEAKER: But the applications of whole genome sequencing are not limited to rare disease and oncology. In some cases, science fiction is becoming reality. In one recent study, rapid whole genome sequencing in neonatal intensive care units was shown to significantly decrease infant mortality, among patients born with serious conditions. Look out for our In Focus "Realizing Precision Medicine with Whole Genome Sequencing" on www.BioTechniques.com. This In Focus, sponsored by Psomagen and featuring their experts, will explore the impact whole genome sequencing is having on precision medicine, the techniques involved, and much more.
SPEAKER: You can follow us on LinkedIn, Facebook, and Twitter to keep up to date with the latest from this In Focus. [MUSIC PLAYING]