A research team, led by Chao Cheng, Ph.D., Assistant Professor in the Department of Genetics at The Geisel School of Medicine at Dartmouth,
used gene expression data from breast cancer patients to computationally infer the presence of different types of immune cells.
A new mathematical model
uses gene expression data to predict where neurons are located throughout the brain
Not exact matches
«Together, our
data strongly suggest that cutaneous
gene therapy with inducible
expression of GLP1 can be
used for the treatment and prevention of diet - induced obesity and pathologies,» the authors wrote.
«We
used the Allen Human Brain Atlas
data to quantify how consistent the patterns of
expression for various
genes are across human brains, and to determine the importance of the most consistent and reproducible
genes for brain function.»
«For several years the potential for the
use of
gene expression data in research and clinical applications has been underappreciated due to the inconsistency of the
data coming from the various types of equipment.
The
data are already being
used to improve
gene information and
expression on VectorBase, a National Institute of Allergy and Infectious Diseases resource center for the scientific community.
Using breast cancer patient
data taken from The Cancer Genome Atlas, molecular biologists Curt M. Horvath and Robert W. Tell
used powerful computational and bioinformatics techniques to detect patterns of
gene expression in two cancer subtypes.
In the Nature Methods paper, Corrada Bravo, UMD computer science doctoral student Florin Chelaru, and undergraduate research assistants from Williams College in Mass. and Washington University in St. Louis
used Epiviz to visualize and analyze DNA methylation and
gene expression data in colon cancer.
Epiviz implements multiple visualization methods for location - based
data (such as genomic regions of interest) and feature - based
data (such as
gene expression),
using interactive
data visualization techniques not available in web - based genome browsers.
Using clinical, genetic, and gene expression data as filters to distinguish genes whose copy number alteration causes cancer from those for whom copy number changes are incidental, the team whittled down their list from 14,000 to a more manageable number, each of which they systematically tested using genetic experiments in ani
Using clinical, genetic, and
gene expression data as filters to distinguish
genes whose copy number alteration causes cancer from those for whom copy number changes are incidental, the team whittled down their list from 14,000 to a more manageable number, each of which they systematically tested
using genetic experiments in ani
using genetic experiments in animals.
The researchers developed algorithms to
use in a «systems biology modeling cycle,» in which they repeatedly fit a model to
gene expression data obtained from laboratory experiments until a good fit was obtained between the predicted and the measured outcomes.
They tested this theory in mice, rats, flies and fish
using publicly available
gene -
expression data.
The organisers
used 884 lymphoblastoid cell lines that had SNP and
gene -
expression data available through the 1000 Genomes Project.
The researchers» next step is to
use the genomic
data they collected from the families — including full genome sequences and
gene expression data — to begin identifying the specific
genes that contribute to risk for bipolar disorder.
In a Cell paper published on April 7, Lanner's team analysed
gene expression in 88 early human embryos and is
using those
data to identify
genes to disrupt in embryos
using CRISPR — Cas9.
HDNetDB allows users to obtain, visualise and prioritise molecular interaction networks
using Huntington's disease - related
gene expression and other types of
data obtained from human samples and other sources.
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.
Using quantitative RT - PCR we confirmed the
expression profile of five
genes (colony - stimulating factor 1 receptor [Csf1r], Cd68, Pex11a, Emr1, and Mcp1) in each of the 24 samples and found excellent agreement between the microarray and RT - PCR
expression data (mean Pearson correlation coefficient = 0.91, microarray versus RT - PCR
expression; Supplemental Table 3, http://www.jci.org/cgi/content/full/112/12/1796/DC1).
To normalize
expression data, we
used multiple internal control
genes as described by Vandesompele et al. (44).
In the current study, the researchers
used infradian cyclic locomotor activity in the mutant mice as a proxy for mood - associated changes, and examined their molecular basis in the brain by conducting prediction analyses of the
gene expression data.
«We analyzed dozens of variants of this
gene and quantitatively measured
expression in about 1,000 embryos, creating a quantitative
data set that could be
used to train mathematical models, utilizing parameter optimization,» Arnosti said.
For
expression analysis in mice, we
used microarray
data as described above to select two internal control
genes, cyclophilin B (Cphn2) and ribosomal protein S3 (Rps3).
The atlas now also includes RNA transcript
data for 27 of these organ - specific tissues
using next generation sequencing, providing a tissue distribution map of both protein and
gene expression.
(Mixture - of - Isoforms) for isoform quantitation
using RNA - Seq is a probabilistic framework that quantitates the
expression level of alternatively spliced
genes from RNA - Seq
data, and identifies differentially regulated isoforms or exons across samples.
Gene Set Enrichment Analysis (GSEA) is a microarray
data - mining technique
used to determine whether there is coordinated differential
expression or «enrichment» in a set of functionally related
genes when comparing control and experimental samples [35].
The new dependency
data complement the Dependency Map team's ongoing efforts to
use functional genomic technologies like CRISPR and RNA interference (RNAi) to locate vulnerabilities that arise within cancer cells as they compensate for the loss of critical
genes due to mutations or
expression changes.
He group is also interested in high throughput
gene expression data analysis, especially
using Bayesian network (BN) approaches.
This section describes the wheat genome assemblies available,
gene models,
using EnsemblPlants to access wheat
data, accessing wheat
expression data, finding variation
data and finding the wheat orthologue of
genes from other species.
We have developed new BN algorithms and tools for analysis of
gene interaction networks
using high throughput
gene expression data.
We applied
gene set enrichment analysis (GSEA)(23) to
expression array
data using KEGG (Kyoto Encyclopedia of
Genes and Genomes) pathways.
We investigate the impact of PMI on
gene expression using data from multiple tissues of post-mortem donors obtained from the GTEx project.
The authors highlight the importance of measuring the variability of transcript
expression and location in so many cells by
using their
data to discover
genes with related functions in the cell.
From these
data, we first measured allele - specific
expression, where a heterozygous site in a
gene can be
used to distinguish
gene expression from the two copies of a
gene.
We have employed exactly the same methodology, but
using the transcript integrity number15 (TIN)
data instead of
gene expression.
To evaluate whether altered
expression of the ABL
genes is associated with breast cancer progression and metastasis, we examined the
expression of ABL1 and ABL2 in normal and invasive breast tumor specimens
using published TCGA (The Cancer Genome Atlas)
data sets (14 — 16).
Members of the TCGA Research Network identified and characterized four glioblastoma subtypes
using gene expression, somatic mutation, and copy number
data.
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.»
The aim of his research was to
use microarray
gene expression data in order to characterize ageing in different human tissues and identify the age at which major changes in genetic
expression profiles occur.
Furthermore, all
data will be presented in a searchable «Tomato
Expression Atlas,» a data - visualizing platform that will link gene expression information with images from a computer tomography (CT) scanner, which uses X-rays to render 3 - D virtual images that include internal s
Expression Atlas,» a
data - visualizing platform that will link
gene expression information with images from a computer tomography (CT) scanner, which uses X-rays to render 3 - D virtual images that include internal s
expression information with images from a computer tomography (CT) scanner, which
uses X-rays to render 3 - D virtual images that include internal structures.
We find evidence of
expression for all VR, and almost all OR
genes that are annotated as functional in the reference genome, and
use the
data to generate over 1100 new, multi-exonic, significantly extended receptor
gene annotations.
Unfortunately these studies
used a different strain of mouse and / or the
gene - level
expression data is not publically available, thus we were unable to compare those abundance estimates with the
data reported here.
Nevertheless, we found OR
gene expression estimates
using this very different technology were consistent with our RNAseq
data, lending support to both methods.
Researchers will
use GTEx
data to follow up on findings from genome - wide association studies and as a resource for the general study of
gene expression networks.
The Bioinformatics group
uses computational methods to analyse genome sequences, amino acid sequences, and
gene expression data, both to identify new
genes of interest and to determine their structure, function and role in the cell.
To annotate the genome, the team generated transcriptome sequence
data — which can be
used to measure
gene expression based on RNA levels — in 12 different tissues types.
We combine biochemical, structural, cellular and functional information
using purified proteins, mutant and transgenic plants, yeast and chemical genomic screening systems, transient
gene expression assays, confocal microscopy and in silico
data analysis to compare ROP - centered kinase signaling during cell polarity (in vitro pollen tubes), morphogenesis (whole plant) and pathogenesis (fungi - infected cells).
Title: Digital spatial profiling platform allows for spatially - resolved, high - plex quantification of mRNA distribution and abundance on FFPE and fresh frozen tissue sections Date / Time: Tuesday, April 17 2018, 8am - 12:00 pm CT Author: Daniel Zollinger, NanoString Poster # / Location: 3434 / Section 18, Board 16 Hyperlink: http://www.abstractsonline.com/pp8/#!/4562/presentation/7119 Digital Spatial Profiling can be
used to obtain high - plex, spatial mRNA
expression data (10's to 100's of
genes) and protein
expression data on FFPE and fresh frozen tissue sections.
In this activity students analyze
data on the
expression of the tb1
gene and
use it to formulate an explanation as to how a specific difference in the corn version of the
gene explains the phenotype of less branching.
Provided
data analysis that included statistics package development with staff statisticians, and high throughput assay advent and development (immediate early
gene expression); Taq - man primer - probe research and design
using primer express.
Moreover,
using a Bayesian deconvolution method to estimate methylation levels from the
data [53], we found promoter methylation levels to be significantly inversely correlated (p value = 2.3e - 25) with previously published
gene expression levels of T cells from human samples (Figure S1).