Using gene mapping and gene validation, researchers from Boston University School of Medicine (BUSM) were able to identify cytoplasmic FMR1 - interacting protein 2 (CYFIP2) as a major genetic risk factor for binge eating.
Using gene mapping techniques, the researchers zeroed in on a mutation in the gene for hypocretin receptor 2.
Not exact matches
The markers have also been
used to produce a detailed
map of the sugarcane genome that shows how the
genes are linked to each other.
In this month's issue of Genome Research, Elizabeth Stewart and her colleagues at Stanford University present this new
map, which places about 8000 landmarks along the genome's 3 billion bases — DNA's building blocks — yielding twice the resolution of
gene maps currently in
use.
To test that idea in the ragworm, Tomer
used a technique he had developed to examine the complex brains of small creatures with unprecedented clarity: He created a high - resolution
map of the worm's brain cells according to the
genes they express, not just their shape and location.
But the genetic factors underpinning seed coat permeability remained a mystery until Ma and his team
used a
map - based cloning approach to hone in on GmHs1 - 1 as the
gene responsible for hard seededness.
To learn more, Zanders and her colleagues
used genetic
mapping to reveal the complex landscape of multiple meiotic drive
genes on chromosome 3 of S. kambucha.
Genes and words have several similarities, and language evolution has conventionally been
mapped using a «family tree» format.
Genetic tools still under construction, such as a haplotype
map that will be
used to discern genetic variation behind common diseases, could further accelerate the search for disease
genes.
With chronically infected mice as their model, the researchers
used a new technology called ATAC - seq to
map the regulatory regions of the genome — the sections of DNA involved in switching
genes on and off — in the animals» exhausted and functional CD8 + T cells.
The new research focused on just nine
genes, those most strongly associated with autism in recent sequencing studies, and investigated their effects
using precise
maps of
gene expression during human brain development.
The vectors are customizable and could potentially be
used as part of a
gene therapy to treat neurodegenerative disorders that affect the entire central nervous system, such as Huntington's disease, or to help
map or modulate neuronal circuits and understand how they change during disease.
By
using random series of 30 nucleotides — the building blocks of RNA and DNA — he thought he could give neurons unique barcodes, linking the barcodes across synapses, then create
maps of their connections
using high - throughput
gene sequencing technology.
«For our new systemic viral vectors — AAV PHP.S and AAV PHP.eB — there are many potential
uses, from
mapping circuits in the periphery and fast screening of
gene regulatory elements to genome editing with powerful tools such as CRISPR - Cas9,» says Gradinaru.
The goal was to make fragments that could be
used to
map genes and sequence the genome.
By
mapping the neural processes involved as birds learn mating songs, scientists hope to someday
use that knowledge to target specific
genes disrupting speech in patients with autism or other neurodevelopmental conditions.
We further assessed ILS
using insertions and deletions (indels)(69), because they have less homoplasy (convergence) than single nucleotides (SM9), and unlike
gene trees, indels can be examined as discrete characters
mapped to a reference tree without the added inference of constructing trees from them.
Using bioinformatics tools to identify and
map out specific components and regulatory interconnections, the study team found highly dynamic activities during CD8 + T cell responses: a distinct repertoire of super enhancers — groups of enhancers that interact with promoters to drive
gene transcription, new groups of enhancers that jump into activity only in the memory cell stage, and extensive re-wiring of regulatory circuits from one cell stage to another.
Using a technique called whole - genome random sequencing, a TIGR team
mapped the entire two - million -
gene sequence of Thermotoga maritima, a bacterium first plucked from hot geothermal springs in Vulcano, Italy.
Positional cloning is a genetic
mapping technique
used to pinpoint the location of specific traits of interest, such as disease - causing
genes or mutations, within the genome.
That
map contains several so - called islands that are unique to A. borkumensis, such as a set of
genes that allow the organism to break down the alkanes in oil and
use them as food.
The
map will help to hunt down disease - causing
genes, which may be
used to design new drugs, diagnose illness, and help vulnerable patients avoid bad drug reactions.
Pairwise alignments were calculated
using Shuffle - LAGAN (window size, 400 bp; step size 40 bp; translated anchoring), a glocal alignment algorithm that is able to calculate optimal alignments by
using both local alignments and global
maps of sequence rearrangements (e.g. duplications of the fiber
gene in adenovirus genomes with 2 fibers)[57].
For example, many studies on human microbiota identify species (or operational taxonomic units) and
map evolutionary relationships
using the 16S ribosomal RNA
gene.
When
mapped to the genome, they tell us not only about the level of expression for various
genes, but also which transcription start sites were
used.
Approach: Wu's group
used Brainbow, a transgenic technique originally devised to
map individual neurons in the brain, to label cells stochastically
using gene cassettes that code for four uniquely expressed fluorescent proteins.
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.
In the present study, to elucidate the neural mechanism underlying this behavior, we
used an immediate early
gene (IEG) to
map the active brain regions of Japanese honeybee workers during the formation of a defensive bee ball.
Genome
mapping is
used to identify and record the location of
genes and the distances between
genes on a chromosome.
Their study
used a pioneering genetic technique to analyse
maps of DNA regions linked to an inherited risk of breast cancer and identify the actual
genes involved in raising a woman's risk.
They
used yeast cells to model the disease, which allowed them to look at over 5,000
genes to
map out which ones caused more or fewer cells to die.
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.
Reads were
mapped to the S. viridis A10.1 reference genome (phytozome.jgi.doe.gov; v1.1)
using TopHat2 (v2.1.0) and an a priori set of 35,214
gene models.
And to do this, she
used the latest technology to sequence the DNA —
map its building blocks to read its
genes.
Global analysis of candidate
genes important for fitness in a competitive biofilm
using DNA - array - based transposon
mapping.
RNA - seq reads from wild - type and mutant libraries were
mapped to the S. viridis reference genome (v1) and annotated
gene models
used to quantify transcript abundances (Supplemental Data Set 3).
The RNA being
used to
map genes in the genome has been obtained from another of Sally's progeny obtained in 2015.
«
Use of peptide tagging to detect proteins expressed from cloned
genes: deletion
mapping functional domains of Drosophila hsp 70.»
The study, «A
gene - based association method for
mapping traits
using reference transcriptome data,» was funded by the National Institutes of Health.
Their contributions to the yeast community include physical
mapping methods, synthetic lethality screen approaches for identifying cross-species candidate
genes as potential cancer drug targets, and a widely
used set of vectors and yeast host strains that have been instrumental in work that has led to countless discoveries in recent decades.
To capture additional spliced reads that remained unmapped, we remapped all unmapped reads against the OGSv2 predicted transcriptome
using the — very - sensitive - local option in bowtie2 [47], and added the counts of reads
mapped to each
gene to the counts derived from the genome
mapping.
This section invites manuscripts describing (a) Linkage, association, substitution or positional
mapping and epigenetic studies in any species; (b) Validation studies of candidate
genes using genetically - engineered mutant model organisms; (c) Studies focused on epistatis and
gene - environment interactions; (d) Analysis of the functional implications of genomic sequence variation and aim to attach physiological or pharmacogenomic relevance to alterations in
genes or proteins; (e) Studies of DNA copy number variants, non-coding RNA, genome deletions, insertions, duplications and other single nucleotide polymorphisms and their relevance to physiology or pharmacology in humans or model organisms, in vitro or in vivo; and (f) Theoretical approaches to analysis of sequence variation.
We then compiled a list of 881 predicted mRNA targets that unambiguously
mapped to unique Entrez
Gene IDs, and performed a number of enrichment analyses using the WebGestalt platform [21] to identify functional categories and pathways overrepresented in this gene l
Gene IDs, and performed a number of enrichment analyses
using the WebGestalt platform [21] to identify functional categories and pathways overrepresented in this
gene l
gene list.
With funding for over a decade from the NSF and the USDA, the Rice Diversity Project supports QTL
mapping, Genome Wide Association Studies (GWAS), and
gene discovery
using a suite of open - source genetic, genomic and bioinformatic resources developed in the McCouch lab.
Using genetic
maps, scientists know that the mutated
gene responsible for this tolerance lies on chromosome 1, now they just need to find it.
Genes affecting autoimmune type 1 diabetes susceptibility in the nonobese diabetic (NOD) mouse (Idd loci) have been
mapped using a congenic strain breeding strategy.
«The Department of Health and its
Gene Therapy Advisory Committee are currently working with other regulators in the field to produce a «Regulatory Route
Map» to provide further clarity on the regulatory requirements for the clinical
use of stem cells.»
The GENSAT project aims to
map the expression of
genes in the central nervous system of the mouse,
using in situ hybridization and transgenic mouse techniques.
Mapping the expression profiles of all
genes one cell at a time revealed unexpected heterogeneity in the stem cell - derived lung cells, and the research team at the CReM
used this information to improve the airway cells engineered in the lab.
The search engine recognizes common
gene identifiers; the conversion to Affymetrix probe set IDs is done
using Ensembl BioMart [77]
mappings.