«The ORIEN network of cancer centers is made up of true partners in data exchange and we are proud to extend these benefits to patients in the form of
genomic data research that will help us better understand cancer at the molecular level and hopefully develop more targeted cancer treatments.»
Not exact matches
The federal government and private organizations have tried to encourage sharing in recent years through initiatives like the
Genomic Data Commons, a «unified data repository» intended to hasten cancer cures by making research pub
Data Commons, a «unified
data repository» intended to hasten cancer cures by making research pub
data repository» intended to hasten cancer cures by making
research public.
There are also forums dedicated to policy issues such as drug pricing and medical standards — last year, former Vice President Joe Biden announced a federal
Genomic Data Commons to expedite cancer
research during a keynote address.
Dr. Eric Topol, a cardiologist and professor of
genomics at the Scripps
Research Institute in California, said there was great potential value in consumer
genomics tests, particularly with services like those developed by Geisinger, Invitae and Sema4 that are backed by strong
data.
These new governance structures must be able to address the concerns of
research participants while at the same time ensuring effective
data sharing that promotes public trust in
genomics research.
Kaye J. (2012) «The tension between
data sharing and the protection of privacy in
genomics research» Annu Rev
Genomics Hum Genet.
This study opens new avenues of
research aiming at integrating
genomic and epigenomic
data together with environmental exposures in order to elucidate the physio - pathological mechanisms underlying asthma and to promote the development of new therapies.
«They are developing the clinical
genomics necessary to foster and support the Precision Medicine Initiative of the National Institutes of Health, and generating the
genomics data that further drives human genome
research.»
The family of the woman whose cells have helped advance a great deal of biological
research has agreed to a case - by - case release of her
genomic data
But the current stance of our major
research institutions maintains that, given time, the ever - accelerating juggernaut of
data from yet more
genomic (and proteomic) projects and brain - scanning studies might somehow drive a causeway of understanding through these so unexpected findings.
A second goal, «unleash the power of
data,» lauds NCI's Genomic Data Commons launched this year, which is collecting cancer research data from many patients in a single datab
data,» lauds NCI's
Genomic Data Commons launched this year, which is collecting cancer research data from many patients in a single datab
Data Commons launched this year, which is collecting cancer
research data from many patients in a single datab
data from many patients in a single database.
Exomes and the Clinical
Research Conundrum: New Approaches to Enhancing the Value of
Genomic Data
The
genomic data allowed the
research team to reconstruct for the first time the spread of the virus across South and Central America, the Caribbean, and into the southern United States.
Added Robert Fulton, director of technology development at Washington University's McDonnell Genome Institute, which contributed to the sequencing and analysis of the
data: «This
research is a great example of the value of comprehensive
genomic analyses and the insights that can be gained from thorough, well - designed studies.
«Progress in
genomic research has already begun to transform modern medicine,» said Tracey DePellegrin, executive editor of G3, which, like its sister journal GENETICS also published by Genetics Society of America, promotes full
data sharing and dissemination for scientific reseachers, «and this progress is contingent on scientists being able to access the
genomic sequences, now available through dbGaP.
Given the huge quantities of
genomic and proteomics
data now being collected by
research hospitals, professionals skilled in sifting that
data for important signals can generate new knowledge of their own.
«Advances in DNA sequencing technologies have enabled NIH to conduct and fund
research that generates ever - greater volumes of GWAS and other types of
genomic data,» said Eric Green, M.D., Ph.D., NHGRI director, report co-author and a co-chair of the trans - NIH committee that developed the GDS policy.
The National Institutes of Health has issued a final NIH
Genomic Data Sharing (GDS) policy to promote data sharing as a way to speed the translation of data into knowledge, products and procedures that improve health while protecting the privacy of research participa
Data Sharing (GDS) policy to promote
data sharing as a way to speed the translation of data into knowledge, products and procedures that improve health while protecting the privacy of research participa
data sharing as a way to speed the translation of
data into knowledge, products and procedures that improve health while protecting the privacy of research participa
data into knowledge, products and procedures that improve health while protecting the privacy of
research participants.
Furthermore, the large volume of
data obtained from their study, which was deposited into a public
genomics data repository, provides a wealth of information available to other researchers to accelerate ALS
research.
Zeggini then did a 1 - year postdoc at Manchester's Centre for Integrated
Genomic Medical
Research, where she honed her skills in statistics and started developing computer - based strategies to analyse
data from complex, multigene studies.
The study analyzed
data from The Cancer Genome Atlas (TCGA), a
research program supported by the National Cancer Institute and National Human Genome Research Institute within the National Institutes of Health that is looking at genomic changes in more than 20 different types of
research program supported by the National Cancer Institute and National Human Genome
Research Institute within the National Institutes of Health that is looking at genomic changes in more than 20 different types of
Research Institute within the National Institutes of Health that is looking at
genomic changes in more than 20 different types of cancer.
Moreover, the
genomic data yielded in this study also lay a solid foundation for our further
research on ESCC.»
Interpretation of genome sequencing
data is a significant challenge because of the volume of
genomic data to sift through, as well as the large, growing body of
research on molecular drivers of cancer and potential targeted therapies.
«Clinical and
research leaders in cancer
genomics are making tremendous progress towards bringing precision medicine to cancer patients, but
genomic data interpretation is a significant obstacle, and that's where Watson can help.»
The initial
data set in CharProtDB was collected through manual literature curation over the years by analysts at the J. Craig Venter Institute (JCVI)[formerly The Institute of
Genomic Research (TIGR)-RSB- as part of their prokaryotic genome sequencing projects.
The overarching goal of his
research is to utilize high - throughput
genomic data sets, mostly based on DNA sequencing, in order to build models that explain how gene expression is regulated.
Jared's
research group focuses on developing new algorithms to analyze large biological
data sets including genome assembly, probabilistic modeling of sequencing
data, the detection of modified bases and the application of
genomics to better understand cancer.
June 6, 2016
Genomic Data Commons at University of Chicago heralds new era of data sharing for cancer research The Genomic Data Commons (GDC), a next - generation platform that enables unprecedented data access, analysis and sharing for cancer research, publicly launched at the University of Chicago on June 6, opening the door to discoveries for this complex set of disea
Data Commons at University of Chicago heralds new era of
data sharing for cancer research The Genomic Data Commons (GDC), a next - generation platform that enables unprecedented data access, analysis and sharing for cancer research, publicly launched at the University of Chicago on June 6, opening the door to discoveries for this complex set of disea
data sharing for cancer
research The
Genomic Data Commons (GDC), a next - generation platform that enables unprecedented data access, analysis and sharing for cancer research, publicly launched at the University of Chicago on June 6, opening the door to discoveries for this complex set of disea
Data Commons (GDC), a next - generation platform that enables unprecedented
data access, analysis and sharing for cancer research, publicly launched at the University of Chicago on June 6, opening the door to discoveries for this complex set of disea
data access, analysis and sharing for cancer
research, publicly launched at the University of Chicago on June 6, opening the door to discoveries for this complex set of diseases.
Tags: big
data, Breast Cancer
Research Program, cancer
genomics, cancer patients,
genomics,
genomics database, metastatic breast cancer, Public Health Sciences, social media
Joshua leads the Human Genetics Informatics team, who are responsible for handling the informatics needs of the Human Genetics
research programme, including processing of large - scale genetics and
genomics data sets.
«Today, making discoveries from cancer
genomic data is challenging because diverse
research groups analyze different cancer datasets using various methods that are not easily comparable,» said GDC principal investigator Robert Grossman, professor of medicine and director of CDIS at UChicago.
The
Genomic Data Commons (GDC), a next - generation platform that enables unprecedented data access, analysis and sharing for cancer research, publicly launched at the University of Chicago on June 6, opening the door to discoveries for this complex set of disea
Data Commons (GDC), a next - generation platform that enables unprecedented
data access, analysis and sharing for cancer research, publicly launched at the University of Chicago on June 6, opening the door to discoveries for this complex set of disea
data access, analysis and sharing for cancer
research, publicly launched at the University of Chicago on June 6, opening the door to discoveries for this complex set of diseases.
The Intel «Cherry Creek» supercomputer — which ranks among the world's fastest and most powerful supercomputers for its combination of speed, power, and energy efficiency — cut down calculation time on complicated analyses from years to days, advancing fields such as
genomics and bioinformatics, medical and climate
research, molecular modeling, and
data analytics.
The Biomedical Genomics group's main line of
research is mining, analysis and re-analysis of
genomic data from biomedical studies.
While enormous amounts of
genomic and clinical
data have been gathered by NCI - funded
research, several barriers have prevented researchers from making full use of them.
The GDC went live with approximately 4.1 petabytes of
data from National Cancer Institute - supported
research programs, including some of the largest and most comprehensive cancer genomics datasets in the world — such as The Cancer Genome Atlas and Therapeutically Applicable Research to Generate Effective Treatments — and more than 14,000 anonymized patien
research programs, including some of the largest and most comprehensive cancer
genomics datasets in the world — such as The Cancer Genome Atlas and Therapeutically Applicable
Research to Generate Effective Treatments — and more than 14,000 anonymized patien
Research to Generate Effective Treatments — and more than 14,000 anonymized patient cases.
TCGA and TARGET taught the
research community the importance of combining patients» medical
data with cancer
genomics data, leading to NCI programs that integrate rich
genomic and clinical datasets.
Research Focus: I am highly trained in producing and purifying monoclonal antibodies from Hybridoma cells, performing ELISA assays, preparing primary cells from organs and analyzing cell populations using FlowJo Cytometry
data analysis software, isolating
genomic DNA from animal tissues, maintaining and screening numerous transgenic and knock out mice lines by PCR and FACS.
They then worked with researchers at the Broad Institute of MIT and Harvard, one of the world's foremost
genomics research labs, to analyze the genetic
data of Arab populations in comparison with European and East Asian populations in relation to susceptibility to rheumatoid arthritis.
«This study is an important step towards developing precision medicine for at - risk and understudied minority populations,» Burchard said, «But the current lack of
genomic data from these populations highlights the urgent need for a dedicated national effort to prioritize diversity in
research.»
As part of Sanford Health, the largest rural non-profit health care system in the nation, we can integrate
research and patient care so that information flows seamlessly — translational
genomic research discoveries are accelerated into clinical applications, such as new treatments and diagnostics to benefit patients, and clinical
data about patient response flows back to the labs to inform more discoveries.
The researchers have made the SWIF (r) code open - source, and they hope that other
research groups will use it to explore
genomic data from populations worldwide.
At the same time,
data sharing is crucial to the success of
genomic research.
The CRS4's Bioinformatics laboratory has access to large clinical sample sets and
genomic data and closely collaborates with hospitals to support clinical researchers in translating basic
research findings into clinical applications.
Improvements in computer memory can be expected to have far - reaching effects on all areas of science and technology, especially by facilitating and extending the application of big
data and
data science in areas from
genomic research to clinical medicine to increasingly general artificial intelligence applications.
PALO ALTO, Calif., April 06, 2016 — Cloudera, the global provider of the fastest, easiest, and most secure
data management and analytics platform built on Apache Hadoop and the latest open source technologies, today announced a collaboration with the Broad Institute of MIT and Harvard, the world's leading biomedical and
genomic research center.
The
research community can explore and familiarize themselves with the quality of these
data sets, review the
data formats provided from our sequencing service, and augment their own
research with additional summaries of
genomic variation across a panel of diverse individuals.
Building the fourth generation of GATK (GATK4) on Cloudera Enterprise and utilizing the Spark distributed computing framework to speed
research, the Broad Institute is facilitating better understanding of
genomic sequencing, resulting in faster
data exploration and ultimately empowering better clinical decisions.
This
data sharing deepens our understanding of variability in the human genome and the genetic underpinnings of disease, leading to advances in
genomics research and
genomic medicine.
The focus of Dr. Smoller's
research interests has been 1) understanding the genetic and environmental determinants of psychiatric disorders across the lifespan; 2) integrating
genomics and neuroscience to unravel how genes affect brain structure and function; and 3) using «big
data», including electronic health records and
genomics, to advance precision medicine.