During the 1990s, a team led by Jeffery Taubenberger at the Armed Forces Institute of Pathology in Washington, D.C.,
sequenced key gene fragments of the 1918 flu strain, recovered from frozen victims found in the Alaskan permafrost and in archived autopsy material.
Not exact matches
Biologists now know that the genome
sequence holds only a small part of the answer, and that
key elements of development and disease are controlled by the epigenome — a set of chemical modifications, not encoded in DNA, that orchestrate how and when
genes are expressed.
The team
sequenced the
gene that codes for the NaV1.7 channel in mole rats, and compared it with SCN9A — a
key gene in the human version of the channel.
To determine how similar a person's fingertip bacteria are to bacteria left on computer
keys, the team took swabs from three computer keyboards and compared bacterial
gene sequences with those from the fingertips of the keyboard owners.
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.
Among the
key elements engineers need to get an organism such as E. coli to make a protein from a synthesized
gene are extra
sequences such as promoters (to help the cell make RNA from DNA) and ribosome binding sites (or RBS, which the cell needs to make proteins from the RNA).
In particular, the comparison of
gene sequences in large numbers of patients and controls will be a
key step in strategies for disease
gene identification.
Researchers have
sequenced the genomes of all 15 species of Darwin's finches, revealing a
key gene responsible for the diversity in the birds» beaks.
After the sections of DNA
sequence have been assembled into a complete genome
sequence we need to identify where the
genes and
key features are, but how do we do this?
April 2012 - New research: Illuminating embryonic stem cells Collaboration between two EU funded projects «Heroic» and «EuroSyStem», has provided new insights into embryonic stem cells The teams used next generation
sequencing technology to examine two
key properties of the cells that influence their identity and behaviour:
gene expression and
gene regulation.
Scientists have now
sequenced the genome of the Mexican axolotl, and have identified a few
key genes hidden amongst its extremely complex genetic blueprint that shed some light on its remarkable regeneration capabilities.
deCODE has identified
key variations in the
sequence of the genome conferring increased risk of major public health challenges from cardiovascular disease to cancer, and employs its
gene discovery engine to develop DNA - based tests to assess individual risk of common diseases; to license its tests and intellectual property to partners; and to provide comprehensive, leading - edge contract services to companies and research institutions around the globe.
The SIGMA project aims to develop novel biomedical approaches to treat this devastating disease by applying powerful
sequencing technologies to discover the
genes and
key pathways underlying common varieties of cancer.
In exploring how proteins interact with crucial DNA
sequences to regulate
gene activity, researchers have shed light on
key biological...
By comparing the promoter
sequences of expressed with non-expressed OR and VR
genes and pseudogenes, it may now be possible to identify
key genomic motifs that control receptor choice.
Viral
gene sequences from an enlarged set of about 200 Epstein - Barr virus (EBV) strains including many primary isolates have been used to investigate variation in
key viral genetic regions, particularly LMP1, Zp, gp350, EBNA1 and the BART miRNA cluster 2.
Over 4 million coding mutations are described in v78 (September 2016), combining genome - wide
sequencing results from 28 366 tumours with complete manual curation of 23 489 individual publications focused on 186
key genes and 286
key fusion pairs across all cancers.
They use natural plant centromeres (a
key part of chromosomes needed for their inheritance), promoters (
gene activation sites), and
gene - termination
sequences to assemble linear or circular minichromosomes that contain at least a dozen
genes that can improve crops by promoting traits like pest and disease resistance.
Since
gene sequencing technology became a
key part of the medical and health sciences around a little over a decade ago, we now understand a lot more about the importance of genetic variations.
Given advances in the rate of DNA
sequencing, the full genetic code of
key crops grown in the two regions could be built very quickly, and the identities and function of their
genes could be determined by relying on similarities to the existing Arabidopsis, rice, and sorghum
sequences and the emerging maize
sequence.