Not exact matches
In a three - stage meta -
analysis, Harvard University neurologist Clemens Scherzer and his collaborators analyzed
gene expression in 410 samples taken
from patients that either had symptomatic or asymptomatic Parkinson's or were healthy, including 185 samples of substantia nigra — a midbrain region where dopamine neurons are particularly susceptible to degeneration.
Scientists
from the Biogerontology Research Foundation (BGRF), a UK - based charity founded to support aging research and address the challenges of a rapidly aging population, propose a new concept for signalome - wide
analysis of changes in intracellular pathways, called OncoFinder, which allows for accurate and robust cross-platform
analysis of
gene expression data.
The three - year study included cell culture studies at Rice as well as a detailed
analysis of
gene -
expression profiles of more than 500 patients
from the Cancer Genome Atlas and protein -
expression profiles
from about 200 MD Anderson patients.
First, samples of leaves
from these plants are collected for in vitro cultures to isolate the fungi; then the DNA and RNA of fungi are extracted to sequence them and, through bioinformatic
analysis, the researcher can determine the
expression, the presence or absence of
genes in the genomes of a species against each other.
The second tool, SuperExactTest, establishes the very first theoretical framework for assessing the statistical significance of multi-set intersections and enables users to compare very large sets of data, such as
gene sets produced
from genome - wide association studies (GWAS) and differential
expression analysis.
This single cell transcriptome
analysis followed by computational
analyses enabled the team to identify the
gene expression profiles of cells in the process of changing
from ES cells to 2CLCs.
An
analysis of all
gene transcription in the cultured cell lines turned up a large
gene complex in which
gene expression differed conspicuously in cells
from patients compared to controls.
A: Sheltzer: Professionally, we're working on a paper together using Joan's data -
analysis ability to parse through
gene -
expression data
from more than 20,000 cancer patients.
Analysis of the most aggressive of these cells revealed a pattern of
gene expression distinct
from that known to occur in breast - to - bone metastasis, as described in an earlier paper by Massagué.
For instance, our «activity centers»
analysis requires translation
from protein or
gene identifiers in a pathway database to Affymetrix probe set identifiers or other
gene expression array platform identifiers.
Our technological expertise ranges
from the most fundamental approaches to study membrane transport in lymphocytes and dendritic cells (subcellular compartmentalization, intravital microscopy, phagosomal functions), the systematic
analysis of
gene expression and it regulation (RNAseq, Chip Seq, proteomics) and physiological and pathological immune responses (mouse models for cancer immunity, immunomodulation / vaccination, human clinical studies in cancer).
A quest to find good primers for
gene expression analysis of Candida albicans
from clinical samples — Gabriela C.Alonso — Journal of Microbiological Methods
Panels B — D. mRNA
expression analysis of
genes involved in glycogen metabolism (Panel B), gluconeogenesis (Panel C), and insulin signaling (Panel D), as quantified by transcriptome
analysis, was performed in enhanced hiPS - HEP cells
from C12, C18, and C22 on Day 12 post-thawing (n = 2 batches per cell line) and compared to
gene expression measurements performed on hphep cells on Day 1 post-thawing (n = 3 donors).
Along with the cellular
genes emphasized
from the microarray
analysis, two
genes that are suspected to be involved in the scleractinian coral calcification process were tested for
expression (Figs. 5A and 5B).
The idea behind our work in bioinformatics is to build on existing methodologies regarding large - scale data
analysis and to develop novel algorithms for processing and merging complex biological data
from multiple sources such as
gene expression data, sequence information, protein - to - protein interaction data, clinico - pathological data etc..
In line with previous studies12, 13,15,17,20 our
analyses show that the investigation of the impact of post-mortem ischemia in tissue transcriptomes is essential to properly interpret
gene expression estimates obtained
from post-mortem tissue samples.
Many million different users consult these databases each year, seeking information on anything
from DNA sequences, protein structures,
gene expression profiles, human genetic polymorphism or even comparative
analyses of entire genomes.
Nick Owens, a post doc in Mike Gilchrist's lab, who developed the computational
analysis, said: «This study improves our ability to understand the way
gene expression changes with time, and
from this we gain insight into the logic of how
gene expression is regulated.
Dr Gilchrist said: «This study suggests that we may improve significantly on the widely used
analysis methods for determining
gene expression levels
from high throughput sequence data: absolute quantitation offers a much sounder basis for determining changes in
gene expression level, a measure widely used to determine the consequence of genetic, chemical or physical disturbances in living systems.»
In small cell lung cancer, starting
from bioinformatics
analyses of large
gene expression datasets, we clustered subsets of co-expressed
gene modules, derived networks of transcription factors and simulated their dynamics using logic - based mathematical modeling.
These webtools make use of the multilayered datasets
from the BXD mouse population to expedite in silico
gene function prediction through a series of integrative and complimentary systems analytical approaches, including (
expression - based) phenome - wide association, transcriptome - / proteome - wide association, and (reverse --RRB- mediation
analysis.
For
analyses of
gene expression in embryos, cryopreserved day 3 embryos and day 6 blastocysts
from 10 IVF / ICSI patients were thawed via an embryo thawing kit (Cooper Surgical) or a blastocyst thawing kit (Cooper Surgical), respectively, according to manufacturer's protocol.
The webtools make use of the multilayered datasets
from the BXD mouse population to expedite in silico
gene function prediction through a series of integrative and complimentary systems analytical approaches, including (
expression - based) phenome - wide association, transcriptome - / proteome - wide association, and (reverse --RRB- mediation
analysis (Figure 1 - 2).
Analyses of macrophages
from Tet2 knockout mice showed elevated
expression of several chemokine and cytokine
genes that contribute to atherosclerosis.
For the
analysis of
gene expression in blastocysts, total RNA was isolated and purified
from three pools of 10 blastocysts produced in vivo or in vitro (KSOM supplemented with 10 % FCS or in the presence of 1 g / L BSA) using the RNeasy Micro Kit (Qiagen)[18].
Indeed, 30 % of all transcripts identified by cap -
analysis of
gene expression (CAGE) tags derived
from human embryonic tissues have been associated with repetitive elements, and 16 % are retrotransposons [14].