Not exact matches
Brains of individuals who died
with Huntington's, Parkinson's or no neurological condition were analyzed using
sequencing technology that provides a data readout of the activity of all
genes in the genome.
Lu's team will extract immune cells called T cells from the blood of the enrolled patients, and then use CRISPR — Cas9
technology — which pairs a molecular guide able to identify specific genetic
sequences on a chromosome
with an enzyme that can snip the chromosome at that spot — to knock out a
gene in the cells.
But the benefits of this
technology for discerning the circuits of the mind go much deeper, because the virus that carries the photoreceptor
genes can also carry promoter
sequences that express their payload only in neurons
with the appropriate molecular address.
Using a novel combination of
technologies, including trio exome
sequencing of patient / parental DNA and genetic studies in the tiny larvae of zebrafish, the EuroEPINOMICS RES consortium found that mutations in the
gene CHD2 are responsible for a subset of epilepsy patients
with symptoms similar to Dravet syndrome — a severe form of childhood epilepsy that is in many patients resistant to currently available anti-epileptic drugs.
«Single - nucleus RNA
sequencing, droplet by droplet: DroNc - Seq,
technology that merges single - nucleus RNA
sequencing with microfluidics, brings new scale to
gene expression studies in complex tissues.»
With the state - of - the - art DNA
sequencing technology used in this study, they will be able to pinpoint the exact mistake in each patient's SS - related
genes.
With the completion of the first phase of the Human Genome Project in 2000, and the advent of
sequencing technologies that can detect
gene variations such as single nucleotide polymorphisms (SNPs), for the first time scientists have the tools in hand to find the key immune
genes and genetic networks that play roles in vaccine response.
She said: «Identifying a fault in Complex I, one of the building blocks of mitochondria which is responsible for causing disease combined
with our custom
gene capture and the latest
sequencing technology means we can screen many more
genes to diagnose this debilitating disease.
The researchers also hope to use
gene sequencing technology to compare the brains of those who have died of Alzheimer's
with those of people who died without neurological diseases, in the hope of finding DNA
sequences of particular microbes in the diseased brains.
A relatively new
technology called exome
sequencing has identified a few families
with novel mutations in their HD
genes.
next - generation DNA
sequencing and
gene and protein array platforms, which allow researchers to perform more comprehensive molecular analyses of tumors, more quickly and accurately, than was possible
with older
technology
Broadly speaking, we are interested in understanding how
genes affect behaviour, but despite rapid advances in
technology for
sequencing and engineering genomes, it is still a challenge to associate particular
genes with heritable behavioural differences because behaviour is time consuming to measure and difficult to quantify.
More recently, in a joint initiative
with the BBMRI - LPC project (Biobanking and Biomolecular Resources Research Infrastructure — Large Prospective Cohorts) and the Wellcome Trust Sanger Institute, the CNAG - CRG launched a call to promote the use of
sequencing technologies for the identification of novel causative variants and
genes and to molecularly diagnose rare disease patients.
Developed in collaboration
with the Laboratory Medicine, Information
Technology and Health Science Research departments of Mayo Clinic Geneticist Assistant NGS Interpretative Workbench, is a web - based tool for the control, visualization, interpretation and historical knowledge base of next generation
sequencing data targeted at specific
genes for the purpose of identifying potentially pathogenic variants associated
with specific conditions such as hereditary colon cancer.
The advent of RNA - seq
technology, in conjunction
with full genome
sequencing, provides a method for the unbiased characterization of
genes regulated by infection in almost any species that can be manipulated in the laboratory.
Research Focus: I dedicate my time and effort to develop high - throughput
sequencing technologies such as single cell transcriptomic, ChIP - Seq, ChIA - PET, and many more... The scientific rational is to understand better and
with a different angle, the mechanisms of epigenetic regulation of
gene expression in (rare) immune cells, pathologically relevant in many diseases such as asthma, SLE, tuberculosis...
The design and engineering of advanced solid - state nanopore materials could allow for the development of novel
gene sequencing technologies that enable single - molecule detection at low cost and high speed
with minimal sample preparation and instrumentation.
The researchers used
gene -
sequencing technology to determine the most common
gene alterations associated
with the cancers and then used their test to find and extract from the fluid cancer the DNA specific to each cancer.
With the development of novel genomics
technologies, such as Next - Generation
Sequencing, numerous new mutations and
gene expression signatures have been identified, allowing us to better understand the molecular heterogeneity of hematologic diseases and to better stratify and assess risk for cancer patients.
Sequencing data, combined
with skilled bioanalytical approaches and an expert team of
gene curators, enables clinicians to access the benefits of the latest genomic advances without having to become
technology experts themselves.
And we now have the capacity to learn more about our
genes than ever before
with the various kinds of genome
sequencing technologies available today.