High-throughput technologies for DNA sequencing and for analyses of transcriptomes,
proteomes and metabolomes have provided the foundations for deciphering the structure …

Substantial opportunities for global health intelligence and research arise from the
combined and optimised use of secondary data within data ecosystems. Secondary data are …

В доступной форме в книге изложены основные события, произошедшие в
медицинской генетике и в молекулярной медицине после расшифровки генома …

Predicting complex human phenotypes from genotypes has recently gained tremendous
interest in the emerging field of consumer genomics, particularly in light of attempting …

Common diseases such as type 2 diabetes and coronary heart disease result from a
complex interplay of genetic and environmental factors. Recent developments in genomics …

Predicting complex human phenotypes from genotypes is the central concept of widely
advocated personalized medicine, but so far has rarely led to high accuracies limiting …

Background About 80% of the roughly 7,000 known rare diseases are single gene
disorders, about 85% of which are ultra-rare, affecting less than one in one million …

This paper analyzes the emergence of 'genomic sovereignty'policies as a newly popular
way for postcolonial countries to frame their investment in genomics. It identifies three …

Aims: This study was designed to obtain data on public understanding of genetic concepts in
the adult population of Western Australia. It explored knowledge of genetic risk of disease …

Background and purpose During the years prior to the turn of the century, scientific and
medical attention for genetic disorders was mainly focused on understanding rare single …