Not exact matches
Utilize turn - key
analysis pipelines and visualization tools for investigating variation within whole
genome, exome and single cell samples.
The genes were identified through population - and
genome - wide linkage scans and association
analyses of at - risk haplotypes
utilizing genetic and clinical data from the 17,000 participants in deCODE's obesity program in Iceland.
Whole
genome association
analysis studies that
utilize single nucleotide polymorphism (SNP) markers have been used to identify the molecular causes of various traits and conditions including genetic mutations within breeds that cause coat color variations [15], hairlessness [25] and defects in spinal development [26].