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What is Genomics - Full Length
Were pleased to present our latest video, What is Genomics? developed in collaboration with Ontario Genomics Institute and Genome British Columbia.
It looks at what genomics means to us and our world and how it relatetes to DNA & genetics, and what studying genomics means to human health, our environment and our knowledge about how we fit into our world.
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What is Genomics?
Genomics
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Barry Schuler: An introduction to genomics
http://www.ted.com What is genomics? How will it affect our lives? In this intriguing primer on the genomics revolution, entrepreneur Barry Schuler says we can at least expect healthier, tastier food. He suggests we start with the pinot noir grape, to build better wines.
TEDTalks is a daily video podcast of the best talks and performances from the TED Conference, where the world's leading thinker
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Introducing Genomics in Healthcare
With new technologies we can now examine the whole of a person's DNA -- their genome -- quicker and cheaper than ever before. In this video, Vivienne Parry OBE introduces the fundamentals of genomics and its growing importance for healthcare.
Health Education England is developing a substantial education programme to inform healthcare professionals about the impact of genomics on clinical practic
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Genomics, Big Data, and Medicine Seminar Series -- Eric D. Green
Eric D. Green, Director, National Human Genome Research Institute (NHGRI) at the National Institutes of Health (NIH) speaks on human genomics, precision medicine, and advancing human health.
Introduction by Eric Schadt, Director, Institute for Genomics and Multiscale Biology, Icahn School of Medicine at Mount Sinai
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Richard Resnick: Welcome to the genomic revolution
http://www.ted.com In this accessible talk from TEDxBoston, Richard Resnick shows how cheap and fast genome sequencing is about to turn health care (and insurance, and politics) upside down.
TEDTalks is a daily video podcast of the best talks and performances from the TED Conference, where the world's leading thinkers and doers give the talk of their lives in 18 minutes. Featured speakers have
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Genomics and Proteomics
In this video, Biology Professor discusses genomics and proteomics, what they are, how they were made possible, and why they are important.
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Envisioning how genomics will improve human health | Illumina Video
In 2014, We asked our employees and thought leaders to share their vision of how genomics will transform our world. The stories are speculative and reflect our hopes for the future. Learn more about Illumina http://www.illumina.com/company.html and how we are unlocking the power of the genome to improve human health.
Illumina is transforming human health as the global leader in sequencing and ar
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Sequencing the Single Cell – Adventures in Genomics
A single cell is the smallest building block in biology. Each and every cell contains an entire genome with all the information to create an entire organism – be it a bacterium or a buffalo cell. Recent advances in sequencing technology are making it possible to extract and sequence the genomes from individual cells. This is advancing our understanding of many biological processes. Subscribe to Il
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Genomics, Big Data, and Medicine Seminar Series – George Church
George Church, Professor, Genetics at Harvard Medical School and Director, PersonalGenomes.org, speaks on "Why Big Data Is Easier than Little Data."
Introductions by Eric Schadt, Director, Institute for Genomics and Multiscale Biology and Jason Bobe, Director, Sharing Lab, Icahn Institute for Genomics and Multiscale Biology.
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Decoding a Genomic Revolution: Manolis Kellis at TEDxCambridge 2013
MIT Computational Biologist Manolis Kellis gives us a glimpse of the doctor's office visit of the future, and uses his own genetic mutations to show us how a revolution in genomics is unlocking treatments that could transform medicine as we know it. Learn more about Manolis Kellis at http://web.mit.edu/manoli and TEDxCambridge at http://www.tedxcambridge.com.
About TEDx, x = independently organiz
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Human Longevity Inc Brad Perkins: genomics close to a breakthrough - Full WIRED Talk
A "supercharged" approach to human genome research could see as many health breakthroughs made in the next decade as in the previous century, says Brad Perkins, chief medical offer at Human Longevity Inc.
"I don’t have a pill" to boost human lifespan, Perkins admitted on stage at WIRED Health 2015. But he has perhaps the next best thing -- data, and the means to make sense of it. Based in San Die
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Genomics, Big Data, and Medicine Seminar Series – Eric J. Topol
Eric J. Topol, MD, Director, Scripps Translational Science Institute speaks on leveraging, developing and testing technology to improve health care.
Introduction by Eric Schadt, Director, Institute for Genomics and Multiscale Biology, Icahn School of Medicine at Mount Sinai
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George Church on the Future of Human Genomics and Synthetic Biology
http://research.ncsu.edu/ges In his talk “The Future of Human Genomics and Synthetic Biology,” Church discussed the exponentially fast pace of emerging genetic technologies (due in part to his own inventions and advancements in the fields of genetics and synthetic biology) and the application of these technologies to present and future work. Synthetic biology, which includes altering gene sequence
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Genomics and Personalized Medicine
(October 20, 2009) Michael Snyder, Professor of Genetics and Chair of the Department of Genetics at Stanford, discusses advances in gene sequencing, the impact of genomics on medicine, the potential for personalized medicine. and efforts at Stanford to further study these issues.
Stanford Mini Med School is a series arranged and directed by Stanford's School of Medicine, and presented by the St
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Big genomic data on Google Cloud Platform
As the cost of DNA sequencing has dropped, the volume of data produced has risen into the petabytes. Google is working with the genomics community to define a standard API for working with big genomic data sets in the cloud. Building on Google Cloud Platform, we show how to store, process, explore and share genomic data using technologies like BigQuery, AppEngine MapReduce, R and more.
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SGI-DNA, A Synthetic Genomics, Inc. Company: Advancing Genomics To Better Life
San Diego is home to Synthetic Genomics, which is revolutionizing biotechnology research by advancing genomics to better life. Founded by world renowned researchers Craig Venter and Hamilton Smith, our expert team of scientists, engineers, and bioinformaticians develop synthetic biology reagents, instruments, informatics tools, and services for our customers and partners, enabling them to research
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Tech Forum at Festival of Genomics: 10X Genomics
10X Genomics present on the Tech Forum Stage at Festival of Genomics Boston 2015
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Genomics: Why Individualized Medicine Matters
The UConn Health Center and The Jackson Laboratory are collaborating to build the future of genomic medicine. The Jackson Laboratory for Genomic Medicine is being built on a 17-acre site on the campus of the University of Connecticut Health Center in Farmington, CT. Together, UConn and JAX will transform medicine by improving care, lowering costs, and increasing life span and health span. JAX Geno
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Genomics of Cancer
Genomics of Cancer
Air date: Wednesday, April 16, 2014, 3:00:00 PM
Category: Wednesday Afternoon Lectures
Runtime: 00:59:56
Description: The understanding of the genetics and genomics of cancer is changing very rapidly. The ability to use next-generation sequencing technologies to dissect the genomes of individual cancer patients is helping to drive this increase in knowledge. In his lecture
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Webinar: Get to know Google Genomics
Learn how Google Genomics can help you store, process, explore, and share genomic data — whether it’s your own or massive shared datasets, like TCGA or Autism Speaks’ MSSNG project. We will talk about why Google is interested in genome data, how our Cloud Platform can make a difference, the GATK pipeline, and other examples of how the service is already being used.
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Kathryn Blair, Ph.D., CPO, Seven Bridges Genomics
The Cancer Pan-Genome in the Cloud
Data produced by cancer genomics research will soon reach exabyte scale, outgrowing current IT approaches to genomic analysis. Moreover, current analytical approaches suffer from “reference bias,” which hinders variant detection generally and in particular the identification of structural variation, known to play an important role in cancer. A cloud-based platfo
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David Haussler: Large-Scale Cancer Genomics
UCSC has built the Cancer Genomics Hub (CGHub) for the US National Cancer Institute, designed to hold data for all major NCI projects. To date it has served more than more than 10 petabytes of data to more than 320 research labs. Cancer is exceedingly complex, with thousands of subtypes involving an immense number of different combinations of mutations. The only way we will understand it is to gat
What is Genomics - Full Length
Were pleased to present our latest video, What is Genomics? developed in collaboration with Ontario Genomics Institute and Genome British Columbia.
It looks at ...
Were pleased to present our latest video, What is Genomics? developed in collaboration with Ontario Genomics Institute and Genome British Columbia.
It looks at what genomics means to us and our world and how it relatetes to DNA & genetics, and what studying genomics means to human health, our environment and our knowledge about how we fit into our world.
wn.com/What Is Genomics Full Length
Were pleased to present our latest video, What is Genomics? developed in collaboration with Ontario Genomics Institute and Genome British Columbia.
It looks at what genomics means to us and our world and how it relatetes to DNA & genetics, and what studying genomics means to human health, our environment and our knowledge about how we fit into our world.
- published: 24 Mar 2010
- views: 40736
Barry Schuler: An introduction to genomics
http://www.ted.com What is genomics? How will it affect our lives? In this intriguing primer on the genomics revolution, entrepreneur Barry Schuler says we can ...
http://www.ted.com What is genomics? How will it affect our lives? In this intriguing primer on the genomics revolution, entrepreneur Barry Schuler says we can at least expect healthier, tastier food. He suggests we start with the pinot noir grape, to build better wines.
TEDTalks is a daily video podcast of the best talks and performances from the TED Conference, where the world's leading thinkers and doers give the talk of their lives in 18 minutes. Featured speakers have included Al Gore on climate change, Philippe Starck on design, Jill Bolte Taylor on observing her own stroke, Nicholas Negroponte on One Laptop per Child, Jane Goodall on chimpanzees, and "Lost" producer JJ Abrams on the allure of mystery. TED stands for Technology, Entertainment, Design, and TEDTalks cover these topics as well as science, business, development and the arts. Watch the Top 10 TEDTalks on TED.com, at http://www.ted.com/index.php/talks/top10
wn.com/Barry Schuler An Introduction To Genomics
http://www.ted.com What is genomics? How will it affect our lives? In this intriguing primer on the genomics revolution, entrepreneur Barry Schuler says we can at least expect healthier, tastier food. He suggests we start with the pinot noir grape, to build better wines.
TEDTalks is a daily video podcast of the best talks and performances from the TED Conference, where the world's leading thinkers and doers give the talk of their lives in 18 minutes. Featured speakers have included Al Gore on climate change, Philippe Starck on design, Jill Bolte Taylor on observing her own stroke, Nicholas Negroponte on One Laptop per Child, Jane Goodall on chimpanzees, and "Lost" producer JJ Abrams on the allure of mystery. TED stands for Technology, Entertainment, Design, and TEDTalks cover these topics as well as science, business, development and the arts. Watch the Top 10 TEDTalks on TED.com, at http://www.ted.com/index.php/talks/top10
- published: 24 Jan 2009
- views: 42459
Introducing Genomics in Healthcare
With new technologies we can now examine the whole of a person's DNA -- their genome -- quicker and cheaper than ever before. In this video, Vivienne Parry OBE ...
With new technologies we can now examine the whole of a person's DNA -- their genome -- quicker and cheaper than ever before. In this video, Vivienne Parry OBE introduces the fundamentals of genomics and its growing importance for healthcare.
Health Education England is developing a substantial education programme to inform healthcare professionals about the impact of genomics on clinical practice. This video is the first educational resource from the programme.
wn.com/Introducing Genomics In Healthcare
With new technologies we can now examine the whole of a person's DNA -- their genome -- quicker and cheaper than ever before. In this video, Vivienne Parry OBE introduces the fundamentals of genomics and its growing importance for healthcare.
Health Education England is developing a substantial education programme to inform healthcare professionals about the impact of genomics on clinical practice. This video is the first educational resource from the programme.
- published: 25 Jun 2014
- views: 11824
Genomics, Big Data, and Medicine Seminar Series -- Eric D. Green
Eric D. Green, Director, National Human Genome Research Institute (NHGRI) at the National Institutes of Health (NIH) speaks on human genomics, precision medicin...
Eric D. Green, Director, National Human Genome Research Institute (NHGRI) at the National Institutes of Health (NIH) speaks on human genomics, precision medicine, and advancing human health.
Introduction by Eric Schadt, Director, Institute for Genomics and Multiscale Biology, Icahn School of Medicine at Mount Sinai
wn.com/Genomics, Big Data, And Medicine Seminar Series Eric D. Green
Eric D. Green, Director, National Human Genome Research Institute (NHGRI) at the National Institutes of Health (NIH) speaks on human genomics, precision medicine, and advancing human health.
Introduction by Eric Schadt, Director, Institute for Genomics and Multiscale Biology, Icahn School of Medicine at Mount Sinai
- published: 25 Mar 2015
- views: 4422
Richard Resnick: Welcome to the genomic revolution
http://www.ted.com In this accessible talk from TEDxBoston, Richard Resnick shows how cheap and fast genome sequencing is about to turn health care (and insuran...
http://www.ted.com In this accessible talk from TEDxBoston, Richard Resnick shows how cheap and fast genome sequencing is about to turn health care (and insurance, and politics) upside down.
TEDTalks is a daily video podcast of the best talks and performances from the TED Conference, where the world's leading thinkers and doers give the talk of their lives in 18 minutes. Featured speakers have included Al Gore on climate change, Philippe Starck on design, Jill Bolte Taylor on observing her own stroke, Nicholas Negroponte on One Laptop per Child, Jane Goodall on chimpanzees, Bill Gates on malaria and mosquitoes, Pattie Maes on the "Sixth Sense" wearable tech, and "Lost" producer JJ Abrams on the allure of mystery. TED stands for Technology, Entertainment, Design, and TEDTalks cover these topics as well as science, business, development and the arts. Closed captions and translated subtitles in a variety of languages are now available on TED.com, at http://www.ted.com/translate.
wn.com/Richard Resnick Welcome To The Genomic Revolution
http://www.ted.com In this accessible talk from TEDxBoston, Richard Resnick shows how cheap and fast genome sequencing is about to turn health care (and insurance, and politics) upside down.
TEDTalks is a daily video podcast of the best talks and performances from the TED Conference, where the world's leading thinkers and doers give the talk of their lives in 18 minutes. Featured speakers have included Al Gore on climate change, Philippe Starck on design, Jill Bolte Taylor on observing her own stroke, Nicholas Negroponte on One Laptop per Child, Jane Goodall on chimpanzees, Bill Gates on malaria and mosquitoes, Pattie Maes on the "Sixth Sense" wearable tech, and "Lost" producer JJ Abrams on the allure of mystery. TED stands for Technology, Entertainment, Design, and TEDTalks cover these topics as well as science, business, development and the arts. Closed captions and translated subtitles in a variety of languages are now available on TED.com, at http://www.ted.com/translate.
- published: 15 Sep 2011
- views: 159921
Genomics and Proteomics
In this video, Biology Professor discusses genomics and proteomics, what they are, how they were made possible, and why they are important....
In this video, Biology Professor discusses genomics and proteomics, what they are, how they were made possible, and why they are important.
wn.com/Genomics And Proteomics
In this video, Biology Professor discusses genomics and proteomics, what they are, how they were made possible, and why they are important.
- published: 10 Sep 2015
- views: 694
Envisioning how genomics will improve human health | Illumina Video
In 2014, We asked our employees and thought leaders to share their vision of how genomics will transform our world. The stories are speculative and reflect our ...
In 2014, We asked our employees and thought leaders to share their vision of how genomics will transform our world. The stories are speculative and reflect our hopes for the future. Learn more about Illumina http://www.illumina.com/company.html and how we are unlocking the power of the genome to improve human health.
Illumina is transforming human health as the global leader in sequencing and array-based technologies. The company serves customers in a broad range of markets, enabling the adoption of genomic solutions in research and clinical settings. Through collaborative innovation, we are fueling groundbreaking advancements in the areas of oncology http://www.illumina.com/applications/cancer.html?sciid=2013211IBN28 , reproductive health http://www.illumina.com/clinical/reproductive-genetic-health.html?sciid=2014243IBN1, genetic disease, http://www.illumina.com/applications/complex-disease-genomics.html?sciid=2013230IBN3,microbiology http://www.illumina.com/applications/microbiology.html?sciid=2013225IBN3 , agriculture http://www.illumina.com/applications/agriculture.html?sciid=2013103IBN3, drug development http://www.illumina.com/applications/genomics-in-drug-development.html?sciid=2014248IBN1, and forensic science http://www.illumina.com/applications/forensics.html?sciid=2013227IBN2.
wn.com/Envisioning How Genomics Will Improve Human Health | Illumina Video
In 2014, We asked our employees and thought leaders to share their vision of how genomics will transform our world. The stories are speculative and reflect our hopes for the future. Learn more about Illumina http://www.illumina.com/company.html and how we are unlocking the power of the genome to improve human health.
Illumina is transforming human health as the global leader in sequencing and array-based technologies. The company serves customers in a broad range of markets, enabling the adoption of genomic solutions in research and clinical settings. Through collaborative innovation, we are fueling groundbreaking advancements in the areas of oncology http://www.illumina.com/applications/cancer.html?sciid=2013211IBN28 , reproductive health http://www.illumina.com/clinical/reproductive-genetic-health.html?sciid=2014243IBN1, genetic disease, http://www.illumina.com/applications/complex-disease-genomics.html?sciid=2013230IBN3,microbiology http://www.illumina.com/applications/microbiology.html?sciid=2013225IBN3 , agriculture http://www.illumina.com/applications/agriculture.html?sciid=2013103IBN3, drug development http://www.illumina.com/applications/genomics-in-drug-development.html?sciid=2014248IBN1, and forensic science http://www.illumina.com/applications/forensics.html?sciid=2013227IBN2.
- published: 09 Jan 2015
- views: 11311
Sequencing the Single Cell – Adventures in Genomics
A single cell is the smallest building block in biology. Each and every cell contains an entire genome with all the information to create an entire organism – b...
A single cell is the smallest building block in biology. Each and every cell contains an entire genome with all the information to create an entire organism – be it a bacterium or a buffalo cell. Recent advances in sequencing technology are making it possible to extract and sequence the genomes from individual cells. This is advancing our understanding of many biological processes. Subscribe to Illumina: http://bit.ly/IlluminaYouTube
Links:
http://www.illumina.com/science/education/adventures-in-genomics.ilmn
Nick Navin at The University of Texas MD Anderson Cancer Center --http://faculty.mdanderson.org/Nicholas_Navin/Default.asp?SNID=2113230403
For more info on applications in cancer - http://www.illumina.com/applications/cancer/research.ilmn
For more info on applications in other areas
http://www.illumina.com/science/publications/publications-review.ilmn
The Adventures in Genomics video series hosted by the Illumina Scientific Affairs team. Embark on a fascinating journey, exploring amazing discoveries and meeting the scientists behind the breakthroughs who are helping us better understand ourselves and the world around us.
See all our Adventures in Genomics videos:
https://www.youtube.com/playlist?list=PLKRu7cmBQlah8wHBByBXEO0dNW-xNvvX_
http://www.Illumina.com
wn.com/Sequencing The Single Cell – Adventures In Genomics
A single cell is the smallest building block in biology. Each and every cell contains an entire genome with all the information to create an entire organism – be it a bacterium or a buffalo cell. Recent advances in sequencing technology are making it possible to extract and sequence the genomes from individual cells. This is advancing our understanding of many biological processes. Subscribe to Illumina: http://bit.ly/IlluminaYouTube
Links:
http://www.illumina.com/science/education/adventures-in-genomics.ilmn
Nick Navin at The University of Texas MD Anderson Cancer Center --http://faculty.mdanderson.org/Nicholas_Navin/Default.asp?SNID=2113230403
For more info on applications in cancer - http://www.illumina.com/applications/cancer/research.ilmn
For more info on applications in other areas
http://www.illumina.com/science/publications/publications-review.ilmn
The Adventures in Genomics video series hosted by the Illumina Scientific Affairs team. Embark on a fascinating journey, exploring amazing discoveries and meeting the scientists behind the breakthroughs who are helping us better understand ourselves and the world around us.
See all our Adventures in Genomics videos:
https://www.youtube.com/playlist?list=PLKRu7cmBQlah8wHBByBXEO0dNW-xNvvX_
http://www.Illumina.com
- published: 26 Aug 2015
- views: 4118
Genomics, Big Data, and Medicine Seminar Series – George Church
George Church, Professor, Genetics at Harvard Medical School and Director, PersonalGenomes.org, speaks on "Why Big Data Is Easier than Little Data."
Introducti...
George Church, Professor, Genetics at Harvard Medical School and Director, PersonalGenomes.org, speaks on "Why Big Data Is Easier than Little Data."
Introductions by Eric Schadt, Director, Institute for Genomics and Multiscale Biology and Jason Bobe, Director, Sharing Lab, Icahn Institute for Genomics and Multiscale Biology.
wn.com/Genomics, Big Data, And Medicine Seminar Series – George Church
George Church, Professor, Genetics at Harvard Medical School and Director, PersonalGenomes.org, speaks on "Why Big Data Is Easier than Little Data."
Introductions by Eric Schadt, Director, Institute for Genomics and Multiscale Biology and Jason Bobe, Director, Sharing Lab, Icahn Institute for Genomics and Multiscale Biology.
- published: 21 Apr 2015
- views: 6600
Decoding a Genomic Revolution: Manolis Kellis at TEDxCambridge 2013
MIT Computational Biologist Manolis Kellis gives us a glimpse of the doctor's office visit of the future, and uses his own genetic mutations to show us how a re...
MIT Computational Biologist Manolis Kellis gives us a glimpse of the doctor's office visit of the future, and uses his own genetic mutations to show us how a revolution in genomics is unlocking treatments that could transform medicine as we know it. Learn more about Manolis Kellis at http://web.mit.edu/manoli and TEDxCambridge at http://www.tedxcambridge.com.
About TEDx, x = independently organized event
In the spirit of ideas worth spreading, TEDx is a program of local, self-organized events that bring people together to share a TED-like experience. At a TEDx event, TEDTalks video and live speakers combine to spark deep discussion and connection in a small group. These local, self-organized events are branded TEDx, where x = independently organized TED event. The TED Conference provides general guidance for the TEDx program, but individual TEDx events are self-organized.* (*Subject to certain rules and regulations)
wn.com/Decoding A Genomic Revolution Manolis Kellis At Tedxcambridge 2013
MIT Computational Biologist Manolis Kellis gives us a glimpse of the doctor's office visit of the future, and uses his own genetic mutations to show us how a revolution in genomics is unlocking treatments that could transform medicine as we know it. Learn more about Manolis Kellis at http://web.mit.edu/manoli and TEDxCambridge at http://www.tedxcambridge.com.
About TEDx, x = independently organized event
In the spirit of ideas worth spreading, TEDx is a program of local, self-organized events that bring people together to share a TED-like experience. At a TEDx event, TEDTalks video and live speakers combine to spark deep discussion and connection in a small group. These local, self-organized events are branded TEDx, where x = independently organized TED event. The TED Conference provides general guidance for the TEDx program, but individual TEDx events are self-organized.* (*Subject to certain rules and regulations)
- published: 25 Sep 2013
- views: 11244
Human Longevity Inc Brad Perkins: genomics close to a breakthrough - Full WIRED Talk
A "supercharged" approach to human genome research could see as many health breakthroughs made in the next decade as in the previous century, says Brad Perkins,...
A "supercharged" approach to human genome research could see as many health breakthroughs made in the next decade as in the previous century, says Brad Perkins, chief medical offer at Human Longevity Inc.
"I don’t have a pill" to boost human lifespan, Perkins admitted on stage at WIRED Health 2015. But he has perhaps the next best thing -- data, and the means to make sense of it. Based in San Diego, Human Longevity is fixed on using genome data and analytics to develop new ways to fight age-related diseases.
Perkins says the opportunity for humanity -- and Human Longevity -- is the result of the convergence of four trends: the reduction in the cost of genome sequencing (from $100m per genome in 2000, to just over $1,000 in 2014), the vast improvement in computational power, the development of large-scale machine learning techniques and the wider movement of health care systems towards ‘value-based’ models. Together these trends are making it easier than ever to analyse human genomes at scale.
Read The Full Story: http://wired.uk/XE09MR
WIRED Health is a one-day summit designed to introduce, explain and predict the coming trends facing the medical and personal healthcare industries. This ambitious inaugural event was held on April 24 2015, at the home of the Royal College of General Practitioners, 30 Euston Square, London.
SUBSCRIBE HERE: http://bit.ly/X6kG5b
For more tech reviews, science explained, gaming news and Wired Talks - visit our website: http://www.wired.co.uk/
To download the Wired UK iPad App: http://bit.ly/W6UsAt
Like Wired UK on Facebook: http://bit.ly/VCGxjy
Follow Wired UK on Twitter: http://bit.ly/TQBDQ7
wn.com/Human Longevity Inc Brad Perkins Genomics Close To A Breakthrough Full Wired Talk
A "supercharged" approach to human genome research could see as many health breakthroughs made in the next decade as in the previous century, says Brad Perkins, chief medical offer at Human Longevity Inc.
"I don’t have a pill" to boost human lifespan, Perkins admitted on stage at WIRED Health 2015. But he has perhaps the next best thing -- data, and the means to make sense of it. Based in San Diego, Human Longevity is fixed on using genome data and analytics to develop new ways to fight age-related diseases.
Perkins says the opportunity for humanity -- and Human Longevity -- is the result of the convergence of four trends: the reduction in the cost of genome sequencing (from $100m per genome in 2000, to just over $1,000 in 2014), the vast improvement in computational power, the development of large-scale machine learning techniques and the wider movement of health care systems towards ‘value-based’ models. Together these trends are making it easier than ever to analyse human genomes at scale.
Read The Full Story: http://wired.uk/XE09MR
WIRED Health is a one-day summit designed to introduce, explain and predict the coming trends facing the medical and personal healthcare industries. This ambitious inaugural event was held on April 24 2015, at the home of the Royal College of General Practitioners, 30 Euston Square, London.
SUBSCRIBE HERE: http://bit.ly/X6kG5b
For more tech reviews, science explained, gaming news and Wired Talks - visit our website: http://www.wired.co.uk/
To download the Wired UK iPad App: http://bit.ly/W6UsAt
Like Wired UK on Facebook: http://bit.ly/VCGxjy
Follow Wired UK on Twitter: http://bit.ly/TQBDQ7
- published: 30 Apr 2015
- views: 5433
Genomics, Big Data, and Medicine Seminar Series – Eric J. Topol
Eric J. Topol, MD, Director, Scripps Translational Science Institute speaks on leveraging, developing and testing technology to improve health care.
Introducti...
Eric J. Topol, MD, Director, Scripps Translational Science Institute speaks on leveraging, developing and testing technology to improve health care.
Introduction by Eric Schadt, Director, Institute for Genomics and Multiscale Biology, Icahn School of Medicine at Mount Sinai
wn.com/Genomics, Big Data, And Medicine Seminar Series – Eric J. Topol
Eric J. Topol, MD, Director, Scripps Translational Science Institute speaks on leveraging, developing and testing technology to improve health care.
Introduction by Eric Schadt, Director, Institute for Genomics and Multiscale Biology, Icahn School of Medicine at Mount Sinai
- published: 19 Jun 2015
- views: 3462
George Church on the Future of Human Genomics and Synthetic Biology
http://research.ncsu.edu/ges In his talk “The Future of Human Genomics and Synthetic Biology,” Church discussed the exponentially fast pace of emerging genetic ...
http://research.ncsu.edu/ges In his talk “The Future of Human Genomics and Synthetic Biology,” Church discussed the exponentially fast pace of emerging genetic technologies (due in part to his own inventions and advancements in the fields of genetics and synthetic biology) and the application of these technologies to present and future work. Synthetic biology, which includes altering gene sequences and expression of genes in living organisms, relies on existing and emerging technologies to manipulate and reconstruct genes and genomes.
Church noted that we have been genetically engineering humans for decades. The first recombinant DNA (DNA joined from different sources) was achieved in the 1970s and paved the way for advances such as gene knock-in and knock-out applications, which are widely used today in biotechnology, medicine, and research. Advances in genome sequencing have also led to targeted gene therapy techniques, including regulation of gene expression using technologies such as RNA interference, which can selectively degrade the messenger RNA of a specific gene or prevent translation of a gene’s mRNA into protein. Church’s own technology, the use of the CRISPR/CRISPR associated protein 9 (Cas9) system to edit specific gene sequences, is a new contender for targeted gene therapy and potential alteration of genomes of entire populations, such as disease transmitting Aedes aegypti mosquitoes.
Many technologies in synthetic biology exist and continue to develop. The difficulty largely lies in deciding which technological implementations to allow. Church noted future applications such as releasing more genetically modified organisms (GMOs)into the wild, altering ageing genes to extend human life, and manipulating genes to help humans adapt to life in space
The GES program is unique example of engaged scholarship that serves as a regional, national, and international hub of interdisciplinary, research analysis and inclusive dialogue surrounding opportunities and challenges associated with genetic engineering and society. It is unique in the nation and world in its blending of approaches from natural sciences, social sciences and humanities. The GES Center provides mechanisms for discussion and rigorous, trustworthy analysis about how products of genetic engineering and synthetic biology may impact society and the environment. Find out more at http://research.ncsu.edu/ges
wn.com/George Church On The Future Of Human Genomics And Synthetic Biology
http://research.ncsu.edu/ges In his talk “The Future of Human Genomics and Synthetic Biology,” Church discussed the exponentially fast pace of emerging genetic technologies (due in part to his own inventions and advancements in the fields of genetics and synthetic biology) and the application of these technologies to present and future work. Synthetic biology, which includes altering gene sequences and expression of genes in living organisms, relies on existing and emerging technologies to manipulate and reconstruct genes and genomes.
Church noted that we have been genetically engineering humans for decades. The first recombinant DNA (DNA joined from different sources) was achieved in the 1970s and paved the way for advances such as gene knock-in and knock-out applications, which are widely used today in biotechnology, medicine, and research. Advances in genome sequencing have also led to targeted gene therapy techniques, including regulation of gene expression using technologies such as RNA interference, which can selectively degrade the messenger RNA of a specific gene or prevent translation of a gene’s mRNA into protein. Church’s own technology, the use of the CRISPR/CRISPR associated protein 9 (Cas9) system to edit specific gene sequences, is a new contender for targeted gene therapy and potential alteration of genomes of entire populations, such as disease transmitting Aedes aegypti mosquitoes.
Many technologies in synthetic biology exist and continue to develop. The difficulty largely lies in deciding which technological implementations to allow. Church noted future applications such as releasing more genetically modified organisms (GMOs)into the wild, altering ageing genes to extend human life, and manipulating genes to help humans adapt to life in space
The GES program is unique example of engaged scholarship that serves as a regional, national, and international hub of interdisciplinary, research analysis and inclusive dialogue surrounding opportunities and challenges associated with genetic engineering and society. It is unique in the nation and world in its blending of approaches from natural sciences, social sciences and humanities. The GES Center provides mechanisms for discussion and rigorous, trustworthy analysis about how products of genetic engineering and synthetic biology may impact society and the environment. Find out more at http://research.ncsu.edu/ges
- published: 29 Oct 2014
- views: 10852
Genomics and Personalized Medicine
(October 20, 2009) Michael Snyder, Professor of Genetics and Chair of the Department of Genetics at Stanford, discusses advances in gene sequencing, the impact ...
(October 20, 2009) Michael Snyder, Professor of Genetics and Chair of the Department of Genetics at Stanford, discusses advances in gene sequencing, the impact of genomics on medicine, the potential for personalized medicine. and efforts at Stanford to further study these issues.
Stanford Mini Med School is a series arranged and directed by Stanford's School of Medicine, and presented by the Stanford Continuing Studies program. Featuring more than thirty distinguished, faculty, scientists and physicians from Stanford's medical school, the series offers students a dynamic introduction to the world of human biology, health and disease, and the groundbreaking changes taking place in medical research and health care.
Stanford University
http://www.stanford.edu
Stanford University School of Medicine
http://med.stanford.edu
Stanford Continuing Studies
http://continuingstudies.stanford.edu
Stanford University Channel on YouTube:
http://www.youtube.com/stanford
wn.com/Genomics And Personalized Medicine
(October 20, 2009) Michael Snyder, Professor of Genetics and Chair of the Department of Genetics at Stanford, discusses advances in gene sequencing, the impact of genomics on medicine, the potential for personalized medicine. and efforts at Stanford to further study these issues.
Stanford Mini Med School is a series arranged and directed by Stanford's School of Medicine, and presented by the Stanford Continuing Studies program. Featuring more than thirty distinguished, faculty, scientists and physicians from Stanford's medical school, the series offers students a dynamic introduction to the world of human biology, health and disease, and the groundbreaking changes taking place in medical research and health care.
Stanford University
http://www.stanford.edu
Stanford University School of Medicine
http://med.stanford.edu
Stanford Continuing Studies
http://continuingstudies.stanford.edu
Stanford University Channel on YouTube:
http://www.youtube.com/stanford
- published: 11 Feb 2010
- views: 26362
Big genomic data on Google Cloud Platform
As the cost of DNA sequencing has dropped, the volume of data produced has risen into the petabytes. Google is working with the genomics community to define a s...
As the cost of DNA sequencing has dropped, the volume of data produced has risen into the petabytes. Google is working with the genomics community to define a standard API for working with big genomic data sets in the cloud. Building on Google Cloud Platform, we show how to store, process, explore and share genomic data using technologies like BigQuery, AppEngine MapReduce, R and more.
wn.com/Big Genomic Data On Google Cloud Platform
As the cost of DNA sequencing has dropped, the volume of data produced has risen into the petabytes. Google is working with the genomics community to define a standard API for working with big genomic data sets in the cloud. Building on Google Cloud Platform, we show how to store, process, explore and share genomic data using technologies like BigQuery, AppEngine MapReduce, R and more.
- published: 25 Jun 2014
- views: 18028
SGI-DNA, A Synthetic Genomics, Inc. Company: Advancing Genomics To Better Life
San Diego is home to Synthetic Genomics, which is revolutionizing biotechnology research by advancing genomics to better life. Founded by world renowned researc...
San Diego is home to Synthetic Genomics, which is revolutionizing biotechnology research by advancing genomics to better life. Founded by world renowned researchers Craig Venter and Hamilton Smith, our expert team of scientists, engineers, and bioinformaticians develop synthetic biology reagents, instruments, informatics tools, and services for our customers and partners, enabling them to research, develop, and commercialize ground-breaking solutions for better sustainability and improved human health.
Learn more at http://sgidna.com
wn.com/Sgi Dna, A Synthetic Genomics, Inc. Company Advancing Genomics To Better Life
San Diego is home to Synthetic Genomics, which is revolutionizing biotechnology research by advancing genomics to better life. Founded by world renowned researchers Craig Venter and Hamilton Smith, our expert team of scientists, engineers, and bioinformaticians develop synthetic biology reagents, instruments, informatics tools, and services for our customers and partners, enabling them to research, develop, and commercialize ground-breaking solutions for better sustainability and improved human health.
Learn more at http://sgidna.com
- published: 11 Dec 2015
- views: 786
Tech Forum at Festival of Genomics: 10X Genomics
10X Genomics present on the Tech Forum Stage at Festival of Genomics Boston 2015...
10X Genomics present on the Tech Forum Stage at Festival of Genomics Boston 2015
wn.com/Tech Forum At Festival Of Genomics 10X Genomics
10X Genomics present on the Tech Forum Stage at Festival of Genomics Boston 2015
- published: 13 Jul 2015
- views: 697
Genomics: Why Individualized Medicine Matters
The UConn Health Center and The Jackson Laboratory are collaborating to build the future of genomic medicine. The Jackson Laboratory for Genomic Medicine is bei...
The UConn Health Center and The Jackson Laboratory are collaborating to build the future of genomic medicine. The Jackson Laboratory for Genomic Medicine is being built on a 17-acre site on the campus of the University of Connecticut Health Center in Farmington, CT. Together, UConn and JAX will transform medicine by improving care, lowering costs, and increasing life span and health span. JAX Genomic Medicine will discover the precise genomic causes of disease; develop individualized diagnostics, treatments and cures; and help build Connecticut's bioscience industry.
The Jackson Laboratory for Genomic Medicine will open in the fall of 2014.
For more information, visit: http://www.jax.org/ct and http://biosciencect.uchc.edu/jackson_laboratory/
wn.com/Genomics Why Individualized Medicine Matters
The UConn Health Center and The Jackson Laboratory are collaborating to build the future of genomic medicine. The Jackson Laboratory for Genomic Medicine is being built on a 17-acre site on the campus of the University of Connecticut Health Center in Farmington, CT. Together, UConn and JAX will transform medicine by improving care, lowering costs, and increasing life span and health span. JAX Genomic Medicine will discover the precise genomic causes of disease; develop individualized diagnostics, treatments and cures; and help build Connecticut's bioscience industry.
The Jackson Laboratory for Genomic Medicine will open in the fall of 2014.
For more information, visit: http://www.jax.org/ct and http://biosciencect.uchc.edu/jackson_laboratory/
- published: 23 Sep 2013
- views: 3483
Genomics of Cancer
Genomics of Cancer
Air date: Wednesday, April 16, 2014, 3:00:00 PM
Category: Wednesday Afternoon Lectures
Runtime: 00:59:56
Description: The understanding...
Genomics of Cancer
Air date: Wednesday, April 16, 2014, 3:00:00 PM
Category: Wednesday Afternoon Lectures
Runtime: 00:59:56
Description: The understanding of the genetics and genomics of cancer is changing very rapidly. The ability to use next-generation sequencing technologies to dissect the genomes of individual cancer patients is helping to drive this increase in knowledge. In his lecture, Dr. Kucherlapati will describe some of the recent advances and how that knowledge is shedding light on the biology of cancer and helping us develop novel therapeutic approaches.
For more information go to http://wals.od.nih.gov
Author: Raju S. Kucherlapati, Ph.D., Paul C. Cabot Professor of Genetics and Professor of Medicine, Harvard Medical School
Permanent link: http://videocast.nih.gov/launch.asp?18395
wn.com/Genomics Of Cancer
Genomics of Cancer
Air date: Wednesday, April 16, 2014, 3:00:00 PM
Category: Wednesday Afternoon Lectures
Runtime: 00:59:56
Description: The understanding of the genetics and genomics of cancer is changing very rapidly. The ability to use next-generation sequencing technologies to dissect the genomes of individual cancer patients is helping to drive this increase in knowledge. In his lecture, Dr. Kucherlapati will describe some of the recent advances and how that knowledge is shedding light on the biology of cancer and helping us develop novel therapeutic approaches.
For more information go to http://wals.od.nih.gov
Author: Raju S. Kucherlapati, Ph.D., Paul C. Cabot Professor of Genetics and Professor of Medicine, Harvard Medical School
Permanent link: http://videocast.nih.gov/launch.asp?18395
- published: 02 May 2014
- views: 1358
Webinar: Get to know Google Genomics
Learn how Google Genomics can help you store, process, explore, and share genomic data — whether it’s your own or massive shared datasets, like TCGA or Autism S...
Learn how Google Genomics can help you store, process, explore, and share genomic data — whether it’s your own or massive shared datasets, like TCGA or Autism Speaks’ MSSNG project. We will talk about why Google is interested in genome data, how our Cloud Platform can make a difference, the GATK pipeline, and other examples of how the service is already being used.
wn.com/Webinar Get To Know Google Genomics
Learn how Google Genomics can help you store, process, explore, and share genomic data — whether it’s your own or massive shared datasets, like TCGA or Autism Speaks’ MSSNG project. We will talk about why Google is interested in genome data, how our Cloud Platform can make a difference, the GATK pipeline, and other examples of how the service is already being used.
- published: 03 Nov 2015
- views: 1064
Kathryn Blair, Ph.D., CPO, Seven Bridges Genomics
The Cancer Pan-Genome in the Cloud
Data produced by cancer genomics research will soon reach exabyte scale, outgrowing current IT approaches to genomic analysi...
The Cancer Pan-Genome in the Cloud
Data produced by cancer genomics research will soon reach exabyte scale, outgrowing current IT approaches to genomic analysis. Moreover, current analytical approaches suffer from “reference bias,” which hinders variant detection generally and in particular the identification of structural variation, known to play an important role in cancer. A cloud-based platform for genomic analysis promises to democratize cancer genomic research and sets the foundation for a novel analytical approach of “Genome Graphs.” This new data structure for genetic sequences can capture a wide range of variation, promising to significantly overcome reference bias and improve our understanding of cancer.
For more information go to PMWCintl.com
wn.com/Kathryn Blair, Ph.D., Cpo, Seven Bridges Genomics
The Cancer Pan-Genome in the Cloud
Data produced by cancer genomics research will soon reach exabyte scale, outgrowing current IT approaches to genomic analysis. Moreover, current analytical approaches suffer from “reference bias,” which hinders variant detection generally and in particular the identification of structural variation, known to play an important role in cancer. A cloud-based platform for genomic analysis promises to democratize cancer genomic research and sets the foundation for a novel analytical approach of “Genome Graphs.” This new data structure for genetic sequences can capture a wide range of variation, promising to significantly overcome reference bias and improve our understanding of cancer.
For more information go to PMWCintl.com
- published: 25 Feb 2015
- views: 287
David Haussler: Large-Scale Cancer Genomics
UCSC has built the Cancer Genomics Hub (CGHub) for the US National Cancer Institute, designed to hold data for all major NCI projects. To date it has served mor...
UCSC has built the Cancer Genomics Hub (CGHub) for the US National Cancer Institute, designed to hold data for all major NCI projects. To date it has served more than more than 10 petabytes of data to more than 320 research labs. Cancer is exceedingly complex, with thousands of subtypes involving an immense number of different combinations of mutations. The only way we will understand it is to gather together DNA data from many thousands of cancer genomes so that we have the statistical power to distinguish between recurring combinations of mutations that drive cancer progression and "passenger" mutations that occur by random chance. Currently, with the exception of a few international research projects, most cancer genomics research is taking place in research silos, with little opportunity for data sharing. If this trend continues, we lose an incredible opportunity. Soon cancer genome sequencing will be widespread in clinical practice, making it possible in principle to study as many as a million cancer genomes. For these data to also have impact on understanding cancer, we must begin soon to move data into a network of compatible global cloud storage and computing systems, and design mech- anisms that allow genome and clinical data to be used in research with appropriate patient consent. The Global Alliance for Genomics and Health was created to address this problem. Our Data Working Group is designing the future of large-scale genomics for cancer and other diseases. This is an opportunity we cannot turn away from, but involves both social and technical challenges.
wn.com/David Haussler Large Scale Cancer Genomics
UCSC has built the Cancer Genomics Hub (CGHub) for the US National Cancer Institute, designed to hold data for all major NCI projects. To date it has served more than more than 10 petabytes of data to more than 320 research labs. Cancer is exceedingly complex, with thousands of subtypes involving an immense number of different combinations of mutations. The only way we will understand it is to gather together DNA data from many thousands of cancer genomes so that we have the statistical power to distinguish between recurring combinations of mutations that drive cancer progression and "passenger" mutations that occur by random chance. Currently, with the exception of a few international research projects, most cancer genomics research is taking place in research silos, with little opportunity for data sharing. If this trend continues, we lose an incredible opportunity. Soon cancer genome sequencing will be widespread in clinical practice, making it possible in principle to study as many as a million cancer genomes. For these data to also have impact on understanding cancer, we must begin soon to move data into a network of compatible global cloud storage and computing systems, and design mech- anisms that allow genome and clinical data to be used in research with appropriate patient consent. The Global Alliance for Genomics and Health was created to address this problem. Our Data Working Group is designing the future of large-scale genomics for cancer and other diseases. This is an opportunity we cannot turn away from, but involves both social and technical challenges.
- published: 28 Feb 2014
- views: 1652