Previous studies on natural resistance to malaria had implicated
a section of human genome near to a cluster of receptor genes.
«New algorithm can pinpoint mutations favored by natural selection in large
sections of the human genome.»
Not exact matches
This consortium selected 44 separate
sections of the
genome that included regions
of high to low gene density and high to low similarity between mouse and
human.
1999 Sara Handros Chull, PhD, MPH Faculty
Section on Ethics
of Genetics and Emerging Biotechnology Department
of Bioethics Clinical Center National Institutes
of Health Director Bioethics Core Office
of the Clinical Director National
Human Genome Research Institute National Institutes
of Health Holly Taylor, PhD, MPH Associate Professor Department
of Health Policy and Management Johns Hopkins Bloomberg School
of Public Health Core Faculty Johns Hopkins Berman Institute
of Bioethics Andrea Kalfoglou, PhD Associate Professor Health Administration and Policy Program Department
of Sociology & Anthropology University
of Maryland, Baltimore County
UNDERSTANDING
HUMAN ACCELERATED REGIONS: Sections of the genome that are largely conserved across mammals and even the entire animal kingdom, but differ in humans, are known as human accelerated regions (H
HUMAN ACCELERATED REGIONS:
Sections of the
genome that are largely conserved across mammals and even the entire animal kingdom, but differ in
humans, are known as
human accelerated regions (H
human accelerated regions (HARs).
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.
He is best known for his discovery that copy - number variation — a state in which cells have an abnormal number
of DNA
sections, sometimes associated with susceptibility or resistance to disease — is widespread and significant in the
human genome.