Sentences with phrase «genomic sequencing services»

The LMM and the Broad CRSP lab offer genomic sequencing services for both clinical diagnostics and to support several genomic medicine research projects including the MedSeq and BabySeq projects and the eMERGE program.

We provide our Genomic Sequencing Services at a discounted rate so that you can purchase interpretations of specific regions of your genome on - demand.

Not exact matches

Wth technology addressing skin microbial therapeutics, fertility science, chronic disease alleviation, post traumatic stress disorder treatments, and services for the biopharmaceutical and clinical research industries; the startups selected by Illumina will have access to the company's genomics and sequencing expertise, business coaching, lab and office space and an infusion of capital.

Currently, his group offers standard genomic services to investigators worldwide, including transcriptomics, whole exome sequencing, and epigenomics.

The Sequencing and Noncoding RNA Program is one of an MDA institution supported shared genomic service resources providing not only instrumentation but also expertise in applications of next generation sequencing and microarray services to invSequencing and Noncoding RNA Program is one of an MDA institution supported shared genomic service resources providing not only instrumentation but also expertise in applications of next generation sequencing and microarray services to invsequencing and microarray services to investigators

Services provided by EMBL Heidelberg include the Core Facilities which provide internal users, collaborators and visitors with access to excellent facilities for high - throughput analysis including microarrays, protein production, mass spectrometry, DNA sequencing, advanced light and electron microscopes and chemical genomics.

The Sequencing and Microarray Facility provides essential genomic analysis services to support researchers in basic science, translational, and populationbased research programs

The CNAG - CRG has an essential role, carrying out clinical grade sequence analysis and piloting the development of a clinical - genomics platform for cancer and rare disease diagnostics for the Catalan Health Service.

When researchers sequenced DNA from nearly a hundred woolly mammoth specimens using genomics service of SciLifeLab, they discovered that the majority of samples came from males.

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.

The Genomics Core is a recent addition to the CCF / LRI Core services community and will provide research groups access to state - of - the - art genomics capabilities (sequencing, genotyping and gene expression arrays).

PLEASANTON, Calif. --(BUSINESS WIRE)-- 10x Genomics, Inc., a company focused on accelerating genomic discovery, today announced a global partnership ecosystem to accelerate customer adoption of 10x Genomics» sequencing applications through the Certified Service Provider and 10x Compatible Programs.

This collaboration builds upon Broad's decade - long experience providing the genomics community with advanced sequencing services, and expands the Institute's offering into data services.

In both projects the CNAG - CRG has an essential role, carrying out clinical grade sequence analysis and piloting the development of a clinical - genomics platform for cancer and rare disease diagnostics for the Catalan Health Service, based on the RD - Connect platform developed at CNAG - CRG in the framework of an EU project.

The HudsonAlpha Clinical Services Lab (CSL) offers personalized genomic sequencing and analysis for the identification of rare undiagnosed and misdiagnosed disease.

These services are aimed to deliver high quality sequencing - ready libraries to map chromatin states (histone modifications), or profile binding of epigenetic modifiers (transcription co-regulators) or DNA binding proteins (transcription factors) on a genomic scale.

The HudsonAlpha Clinical Services Lab, in collaboration with Illumina, serves as the whole genome sequencing core for the Undiagnosed Disease Network (UDN), a National Institutes of Health - funded study to diagnosed rare and new diseases through the use of genomics and other advanced technologies.

The HudsonAlpha Clinical Services Lab leverages the expertise of the HudsonAlpha Institute for Biotechnology's highly - experienced scientists, clinicians, and analysts working in one of the top four genomic sequencing laboratories in the United States.

HudsonAlpha Clinical Services Lab was established in 2015 in response to the growth of the field of genomic medicine and increased demand for sequencing.

Eurofins MWG Operon Biotechnologies, Huntsville • AL 2008 — 2009 Genomic Information Services / DNA Sequencing Associate Demonstrated extensive knowledge of SANGER method of high throughput DNA sequencing and DNA preparation, primer design, and data analysis using 3730xL ABI Data Collection software and knowledge of 3730xL ABISequencing Associate Demonstrated extensive knowledge of SANGER method of high throughput DNA sequencing and DNA preparation, primer design, and data analysis using 3730xL ABI Data Collection software and knowledge of 3730xL ABIsequencing and DNA preparation, primer design, and data analysis using 3730xL ABI Data Collection software and knowledge of 3730xL ABI machines.