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- Impact of Genomic Variation on Function (IGVF) Consortium1
- Encyclopedia of DNA Elements (ENCODE) Project1
- Genomics Research to Elucidate the Genetics of Rare Diseases (GREGOR) Consortium1
- Multi-Omics for Health and Disease (Multi-Omics)1
- Ethical, Legal and Social Implications (ELSI) Research Program4
- Genomics-Enabled Learning Health Systems (gLHS)1
Educational Resources
A fibroblast is the most common type of cell found in connective tissue.
… Fibroblast … A fibroblast is the most common type of cell found in connective tissue. … Cell Biology, Wound Healing … A fibroblast is a type of cell that contributes to the formation of connective … of that individual. … A fibroblast is the most common type of cell found in connective tissue. … Educational …
Educational Resources
A phenotype is an individual's observable traits, such as height, eye color, and blood type.
… observable traits, such as height, eye color, and blood type. … Gene, Heterozygous, Homozygous, Allele, Trait, … observable traits, such as height, eye color and blood type. A person’s phenotype is determined by both their … observable traits, such as height, eye color, and blood type. … Educational Resources …
Secondary Genomics Findings Service
Responsibilities as a PI, consent, type of data accepted, and how to apply
… my participants to receiving secondary findings? … What type of data does the SGFS accept? … How do I apply? … What … before applying? … Responsibilities as a PI, consent, type of data accepted, and how to apply … Responsibilities as a PI, consent, type of data accepted, and how to apply … Secondary Genomics …
News Release
Researchers from The Cancer Genome Atlas Research Network identify novel mutations in a well-known cancer-causing pathway in lung adenocarcinoma.
… main risk factor, adenocarcinoma is also the most common type of lung cancer among lifelong non-smokers and the risk … Study identifies novel genomic changes in the most common type of lung cancer … Researchers from The Cancer Genome …
Educational Resources
Substitution is a type of mutation where one base pair is replaced by a different base pair.
… Substitution … Substitution is a type of mutation where one base pair is replaced by a … Mutation … Substitution, as related to genomics, is a type of mutation in which one nucleotide is replaced by a … a protein with a different amino acid. … Substitution is a type of mutation where one base pair is replaced by a …
Educational Resources
Duplication is a type of mutation that involves the production of one or more copies of a gene or region of a chromosome.
… Duplication … Duplication is a type of mutation that involves the production of one or more … … Duplication, as related to genomics, refers to a type of mutation in which one or more copies of a DNA segment … genomes of humans and other organisms. … Duplication is a type of mutation that involves the production of one or more …
Educational Resources
Messenger RNA (abbreviated mRNA) is a type of single-stranded RNA involved in protein synthesis.
… RNA (mRNA) … Messenger RNA (abbreviated mRNA) is a type of single-stranded RNA involved in protein synthesis. … … Cell Biology … Messenger RNA (abbreviated mRNA) is a type of single-stranded RNA involved in protein synthesis. … protein chain. … Messenger RNA (abbreviated mRNA) is a type of single-stranded RNA involved in protein synthesis. … …
Educational Resources
Translocation is a type of chromosomal abnormality in which a chromosome breaks and a portion of it reattaches to a different chromosome.
… Translocation … Translocation is a type of chromosomal abnormality in which a chromosome breaks … genetic diseases and disorders. … Translocation is a type of chromosomal abnormality in which a chromosome breaks …
Educational Resources
Single nucleotide polymorphisms (SNPs) are a type of polymorphism involving variation of a single base pair.
… (SNPs) … Single nucleotide polymorphisms (SNPs) are a type of polymorphism involving variation of a single base … traits. … Single nucleotide polymorphisms (SNPs) are a type of polymorphism involving variation of a single base …
Genetic Disorders
Spinal muscular atrophy is a group of inherited disorders that cause progressive muscle degeneration and weakness.
… before the age of 1 year. There are two types of SMA, type IV and Finkel type, that occur in adulthood, usually after age 30. Symptoms … Muscular Atrophy, Tremors, Twitching, Type 1 SMA, Type 2 SMA, Type 3 SMA … Spinal muscular atrophy is a group of …