Results from a statistical analysis shows a cluster of SNPs — single nucleotide polymorphisms — in one
section of a single gene, indicating the location of a mutation likely linked to autism.
Not exact matches
It is typically less expensive to get preselected information about the 20,000 or so
genes that make up a person's exome — the
section of the genome that provides instructions for making proteins — than to perform a more precision - oriented test that targets a
single gene.
Bethesda, USA (2016 - present) Research areas: Super-resolution microscopy,
single - molecule imaging,
gene expression, computational modeling and data analysis This
section includes all projects during my postdoctoral research stay at the National Institutes
of Health in Bethesda, MD (Unites States): (9) Understanding
gene expression in eukaryotic cells»
«Trying to find a
single causative
gene for diseases with a complex genetic background is like looking for the proverbial needle in a haystack,» says Lea Davis, PhD,
of the
section of Genetic Medicine at the University
of Chicago, co-corresponding author
of the PLOS Genetics report.
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.