Not exact matches
Among other initiatives, his group contributes to ENCODE (Encyclopedia
of DNA Elements), supported by NIH to define functional genomic elements; the DOE Systems Biology Knowledgebase (KBase) for data sharing and
analysis; and the internationally funded 1000 Genomes Project on
human genetic variation.
Furthermore, the
analysis of data on single - nucleotide polymorphisms, the main cause
of difference between
human beings, allows the prediction
of phenotypic effects
of a particular
genetic variation.
He is interested in elucidating mechanisms
of human disease by exploring the functional effects
of genetic variation through computational
analysis of «- omic» sequencing data.
We show how the HapMap resource can guide the design and
analysis of genetic association studies, shed light on structural
variation and recombination, and identify loci that may have been subject to natural selection during
human evolution.
DNA methylation
analysis of multiple tissues from newborn twins reveals both
genetic and intrauterine components to
variation in the
human neonatal epigenome
The researchers used the very large survey
of human genetic variation called HapMap for their
analysis, which compared
human variations with the chimpanzee genome.
The Broad Institute and its collaborating institutions have received two major grants from the National
Human Genome Research Institute (NHGRI) that will support the use
of genome sequencing and
analysis to identify the genes and
genetic variation that underlie both rare and common diseases.
Mesh terms: Adolescent Age Factors Age
of Onset Antisocial Personality Disorder Attention Deficit Disorder with Hyperactivity Birth Weight Catechol O - Methyltransferase Child Child, Preschool Female
Genetic Variation Genotype
Humans Infant, Newborn Male Prefrontal Cortex Pregnancy Prenatal Exposure Delayed Effects Psychiatric Status Rating Scales Regression
Analysis Risk Factors Valine