Over the summer, I wrote a post emphasizing the importance of
clinical sequence data sharing in repositories like the ClinSeq database, which has already proven life - saving (or life - changing) for thousands of patients and their families.
Not exact matches
Participants in United Therapeutics»
clinical trials now have their genomes
sequenced and researchers at the company plan to correlate patient outcomes with that genomic
sequence data.
During his speech, Biden repeatedly stressed the importance of breaking down the regulatory and structural barriers to pooling
clinical trial and genomic cancer
sequencing data.
In a study that included children and young adults with relapsed or refractory cancer, incorporation of integrative
clinical genomic
sequencing data into
clinical management was feasible, revealed potentially actionable findings in nearly half of the patients, and was associated with change in treatment and family genetics counseling for a small proportion of patients, according to a study in the September 1 issue of JAMA.
Researchers working with stem cells should follow the example of their colleagues in genetic
sequencing and
clinical research, setting up global networks for sharing
data, materials, and intellectual property, according to a report released today in Washington, D.C..
To this purpose, GenProfile utilizes a powerful technology platform, which involves proprietary high - throughput technologies for gene
sequence comparison (e.g., multiplex
sequence comparison), genotyping (MALDI - TOF minisequencing), unique approaches to
data analysis and interpretation, as well as a large network of
clinical collaborators.
The Johns Hopkins team tested ImmunoMap's ability to correlate immune responses on receptor
sequencing data from T - cells in the tumors of 34 patients with cancer enrolled in a nationwide
clinical trial of the immunotherapy drug nivolumab.
Professor Jean - Claude Dujardin from ITM points out: «It took us more than five years to collect an unprecedented
sequencing data set from
clinical isolates in the Indian sub-continent and publish a first analysis last year.
«The different
clinical presentations, and some very preliminary [DNA]
sequencing data, suggest that the Hendra virus may be somewhat different in this outbreak,» says epidemiologist Hume Field of the Australian Biosecurity Cooperative Research Centre for Emerging Infectious Diseases in Brisbane.
«We retrospectively analyzed the
data from the DTI
sequence to derive measures of white matter integrity, which we compared to
clinical measures and subsequent outcome measures 6 months to 2.5 years after the initial evaluation.»
In the case of
clinical next - generation
sequencing, and in genetic cohort studies and biobanks, pertinent issues include the interpretation of
data,
data storage,
data sharing, informed consent and identifiability / privacy [20][26].
It will house
data from a new era of programs that will
sequence the DNA of patients enrolled in NCI
clinical trials.
Researchers are building a database of DNA
sequence, functional and epigenomic information, and
clinical data from studies on type 2 diabetes and its macro - and microvascular complications, and creating analytic tools to analyze these
data.
Essential systems are now in place to isolate and
sequence pathogens from many thousands of
clinical samples per year, generating an unprecedented amount of raw genetic
data.
«It's amazing to see studies going on at multiple locations in the Mekong region, where precise
clinical measurements are being made in patients undergoing treatment for malaria, and within a few months these
clinical data are connected to genome
sequence data on the parasites,» says Professor Dominic Kwiatkowski, CGGH Director, as he reflects on the strength of the collaboration with TRAC.
Cell biology has continued to expand ever since, extending its impact on
clinical medicine and pharmacology while drawing on new technologies in bioengineering, high - resolution imaging, massive
data handling, and genomic
sequencing.
EPIC is a longitudinal study at UCSF that is tracking nearly 600 patients for ten years using
clinical evaluations, blood draws, imaging
data, and full genome
sequencing.
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.
PHG Foundation has previously carried out work examining the implications of whole exome and genome
sequencing on
clinical services which identified
data sharing as a key priority for these technologies to be deployed effectively for
clinical benefit.
The CGGH is leading this area of analysis by integrating the
clinical data with genome
sequencing data on 1,000 parasite samples collected by the study.
The MRC Centre for Genomics and Global Health (CGGH) is supporting TRAC by leading a genome - wide association study and population genetic analysis that integrates TRAC
clinical data with genome
sequencing data generated through a partnership with MalariaGEN and the Wellcome Trust Sanger Institute.
Developing standards and procedures for the use of
sequencing information in
clinical medicine is an urgent need with numerous obstacles to integrity and storage of
sequencing data, interpretation, and responsible
clinical integration.
Genome
sequencing of the TRAC
clinical samples has now been completed, generating terabytes of
data that were processed by the
sequence - analysis pipeline team led by Jim Stalker, to produce quality - controlled information about many thousands of variants for each sample.
This project produced
data demonstrating that 185 CHIKV
sequences associated with the 2014 Caribbean outbreak segregate into 2 well - supported clades, that multiple phylogenetic subclades are associated with
clinical phenotypes, and that multiple international transmission events were observed.
Yet I can also tell you that they're inherently noisy — particularly for targeted
sequencing data — and I would not be confident in using them to guide
clinical care.
Analyzes whole genome and detailed
clinical data from nearly 300,000 Icelanders Finds several novel variations in the
sequence of the human genome modulating cholesterol levels Five variants are also causally linked to increased risk of coronary artery disease Shows...
Clinical Studies: Our clinical core, led by Dr. Kurt Christensen, conducts economic analyses alongside prospective clinical studies to better understand the full costs of sequencing and to collect real - world data about health care utilization and clinical outcomes following genomi
Clinical Studies: Our
clinical core, led by Dr. Kurt Christensen, conducts economic analyses alongside prospective clinical studies to better understand the full costs of sequencing and to collect real - world data about health care utilization and clinical outcomes following genomi
clinical core, led by Dr. Kurt Christensen, conducts economic analyses alongside prospective
clinical studies to better understand the full costs of sequencing and to collect real - world data about health care utilization and clinical outcomes following genomi
clinical studies to better understand the full costs of
sequencing and to collect real - world
data about health care utilization and
clinical outcomes following genomi
clinical outcomes following genomic tests.
Critical
data gathered from the NSIGHT projects will help to address technical, medical, behavioral and economic questions surrounding newborn
sequencing — and ultimately, will aid in the development of best
clinical practices and provide guidance on the implementation of
sequencing in newborns.
Microsatellite genotypes were obtained for 203
clinical infection samples from eight locations, and Illumina paired - end
sequences were obtained to yield high coverage genome - wide single nucleotide polymorphism (SNP)
data for 65
clinical infection samples from four locations.
Topics that will be explored include: • Cellular and developmental origins of pediatric cancer • Key findings of pan-cancer analysis efforts • Computational pipelines to analyze large - scale
sequencing data • Opportunities for leveraging existing cancer genomics datasets • Strategies for integrative analysis of germline and somatic variants • Correlation of germline / somatic variation to
clinical features such as tumor subtype.
In addition to the functional
data, high - resolution structural images were obtained using a standard
clinical T1 - weighted
sequence.
The aim of this study was to evaluate the correlation between antimicrobial resistance (AMR) profiles of 96
clinical isolates of Actinobacillus pleuropneumoniae, an important porcine respiratory pathogen, and the identification of AMR genes in whole genome
sequence (wgs)
data.
Increasingly, MLST is being performed using next - generation
sequencing (NGS)
data by reference laboratories and for
clinical diagnostics.
Kp isolated from screening swabs and
clinical diagnostic samples were characterized using whole genome
sequencing and combined with epidemiological
data to identify likely transmission events.
All
data of the PedBrain - Tumor consortium including all
sequence data generated by the
sequencing work packages (WP5 - 9) and histopathological and
clinical annotations will be stored in this
data center.
Tags for this Online Resume: Research, Infectious Diseases, Statistics, Medical Devices, Spine, Orthopedics, Sales, Pennsylvania,
Clinical Research Manager, Biology, Immunological Assays, Client Relations, Social Media, Large - Scale Studies, Vaccines, Market Analysis, Event Planning, Sales Cycle Management,
Data Analyses, qPCR, Genome
Sequencing, Global Research, Journal Publications, Published Writer, Media Relations, Presenatations, Team Leadership
His current work focuses on the development and evaluation of novel molecular biology,
sequencing and bioinformatics methods to aid the interpretation of genome and metagenome scale
data generated in
clinical and public health microbiology.