Search Results
Educational Resources
Non-directiveness refers to the nature of the genetic counseling process.
… to the nature of the genetic counseling process. … Carrier Screening, Birth Defect, Genetic Screening, Genetic Testing, Family Health History, Newborn Screening, Genetic Counseling … … Non-directiveness refers …
News Release
Nurses and other health professionals looking to integrate genomics into patient care now have access to an online toolkit with more than 100 resources.
News Release
NIH will award nearly $80 million to support the establishment of the Mendelian Genomics Research Consortium and the development of novel methods and approaches that help researchers identify the genetic causes of single-gene diseases.
… Genomics Research Consortium and the development of novel methods and approaches that help researchers identify the … primary goal is to explore and find innovative methods to increase the rate at which the genes responsible … Genomics Research Consortium and the development of novel methods and approaches that help researchers identify the …
News Release
NIH lost a key member of its broader genomics team when Robert Blakesley, Ph.D., director of the NISC sequencing group at NIH, retired on Dec. 31, 2015.
… and for valuable introductions to those working in the large genome sequencing centers around the world. "NISC … Blakesley. "We were in almost constant contact with the large genome sequencing centers at Washington University, the …
News Release
Researchers from NHGRI, Oxford University and other National Institutes of Health centers have developed and tested a new method to predict hospital-acquired infections involving five other important pathogens.
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.
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.
Talking Glossary
Next-generation DNA sequencing (abbreviated NGS) refers to the use of technologies for sequencing DNA that became available shortly after the completion of the Human Genome Project (which relied on the first-generation method of Sanger sequencing).
Talking Glossary
While some sequencing technologies produce reads that are only a few hundred nucleotides long, some methods can generate reads that are thousands to hundreds of thousands of nucleotides long, known as “long-read DNA sequencing.”
… reads that are only a few hundred nucleotides long, some methods can generate reads that are thousands to hundreds of … reads that are only a few 100 nucleotides long, some methods can generate reads that are thousands to hundreds of … reads that are only a few hundred nucleotides long, some methods can generate reads that are thousands to hundreds of …
For Patients and Families
Genetic tests may be used to identify increased risks of health problems, to choose treatments, or to assess responses to treatments.
… Genetic testing uses laboratory methods to look at your genes, which are the DNA instructions … help identify fetuses that have certain diseases. Newborn screening is used to test babies one or two days after birth … assess responses to treatments. … Genetic Testing, Newborn Screening, Diagnosing A Genetic Condition, Genetic Disease … …