In two recent publications, researchers have used data and samples from the 1000 Genomes Project to study arthritis, osteoarthritis and rheumatoid arthritis.
read moreIn two recent publications, researchers have used data and samples from the 1000 Genomes Project to study cardiovascular disease.
read moreIncluded are two recent publications where researchers have used data and samples from the 1000 Genomes Project to study cancer.
read moreTwo recent publications have used data and samples from the 1000 Genomes Project to study pharmacogenetics. Pharmacogenetics is the study of genetic variation that impacts how we respond to medications.
read moreIn two recent publications, researchers used data from the 1000 Genomes Project to study cancer.
read moreTwo recent publications have used data from the 1000 Genomes Project to study Alzheimer’s disease.
read moreTwo recent studies used data from the 1000 Genomes Project to investigate inherited risk for heart disease in children and adults.
read moreThe NIGMS Human Genetic Cell Repository (HGCR) and NHGRI Sample Repository for Human Genetic Research (SRHGR) now offer high molecular weight (HMW) DNA samples isolated from cell lines in the collections. HMW DNA is useful for long-read next-generation sequencing and studies that investigate large-scale genomic variation such as structural variation.
read moreTwo recent studies used data from the 1000 Genomes Project to study polygenic risk scores, which use genetic information from many genes across the genome to predict inherited risk of developing common, complex diseases.
read moreIn a study published in the journal Infection, Genetics and Evolution, scientists analyzed genetic variants from publicly available datasets including the 1000 Genomes Project to determine whether differences in genetic variation across populations may account for the observation that certain populations and ethnic groups are disproportionately affected by COVID-19.
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