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Talking Glossary
Cell-free DNA testing is a laboratory method that involves analyzing free (i.e., non-cellular) DNA contained within a biological sample, most often to look for genomic variants associated with a hereditary or genetic disorder.
… Cell-Free DNA Testing … Cell-free DNA testing is a laboratory method that involves analyzing free … with a hereditary or genetic disorder. … Cell-free DNA testing is a laboratory method that involves analyzing free …
15 Ways Genomics Influences Our World
Genomics is revolutionizing health assessments before birth.
… be a stressful time, and for many years prenatal genetic testing has required invasive procedures with associated … Less than a decade ago, women seeking prenatal genetic testing, such as for a condition like Down syndrome, had to … has allowed a totally new approach for prenatal genetic testing, at least for the initial screening test for a new …
News Release
NIH researchers have developed a breath test that measures how well patients with methylmalonic acidemia (MMA) respond to receiving liver or combined liver and kidney transplantation.
15 Ways Genomics Influences Our World
Advances in genomics are helping you access information about your genome from your home.
… an explosion in at-home, or "direct to consumer" genomic testing. You can even seek genomic information without … to learn more about yourself or your family through DNA testing - maybe you've seen ads on TV or heard them on the … radio. The global "direct-to-consumer" (or DTC) genomic testing market was valued at $117 million in 2017, suggesting …
News
To prevent an emerging genomic technology from contributing to health disparities, a scientific team funded by the National Institutes of Health has devised new ways to improve a genetic testing method called a polygenic risk score.
… of Health has devised new ways to improve a genetic testing method called a polygenic risk score . Since … of Health has devised new ways to improve a genetic testing method called a polygenic risk score. … To prevent an … of Health has devised new ways to improve a genetic testing method called a polygenic risk score. … News …
News Release
A simple blood draw is replacing a giant needle to the belly for testing their fetuses for a range of genetic disorders.
… blood draw is replacing a giant needle to the belly for testing their fetuses for a range of genetic disorders. This … by amniocentesis . That's part of the problem: this new testing could include a broader range of results such as … blood draw is replacing a giant needle to the belly for testing their fetuses for a range of genetic disorders. … …
Educational Resources
Carrier screening is a genetic test performed on people who display no symptoms for a genetic disorder but may be at risk for passing it on to their children.
… be at risk for passing it on to their children. … Genetic Testing, Genetic Disorder, Alleles, Inheritance, Family Health History … Carrier screening involves testing to see if a person “carries” a genetic variation …
Fact Sheets
Newborn screening tests use a dried blood sample collected during the first week after birth to measure the presence of disease biomarkers.
… genome sequencing in addition, or instead of, existing testing programs? Are there additional considerations to … of disease biomarkers. … Newborn Screening, Genetic Testing, Healthcare, Genetic Material, Gene Mutation, Genes … …
Event
The Inter-Society Coordinating Committee for Practitioner Education in Genomics (ISCC-PEG) will hold its 11th annual meeting online on February 16, 2022.
… its 11th annual meeting. … ISCC-PEG 11th Annual Meeting (Virtual) … The Inter-Society Coordinating Committee for …
Event
The Inter-Society Coordinating Committee for Practitioner Education in Genomics (ISCC-PEG) will hold its10th annual meeting online on February 16, 2021.
… its 10th annual meeting. … ISCC-PEG 10th Annual Meeting (Virtual) … The Inter-Society Coordinating Committee for …