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About Genomics
Resources for understanding the first truly complete sequence of the Y chromosome, the final human chromosome to be fully sequenced.
News Release
Evaluating genetic features of inherited diseases by sequencing the genetic code helps with the cost and time challenges in medical practice.
… all potential genetic features of inherited diseases by sequencing the genetic code is a powerful solution to … get in there and start touching patient data." Through new sequencing technologies, data is accumulating in an … M.D., Ph.D. But how do we make sure that using genome sequencing for disease diagnosis, treatment and prevention …
Educational Resources
A mutation is a change in a DNA sequence. Mutations can result from DNA copying mistakes made during cell division, exposure to ionizing radiation, exposure to chemicals called mutagens, or infection by viruses.
News Release
Extending noninvasive prenatal screening to all 24 human chromosomes can detect genetic disorders that explain miscarriage and abnormalities during pregnancy.
… tested for during pregnancy. New research suggests sequencing all 24 chromosomes to uncover other, rare … Rare Autosomal Trisomies, Revealed by Maternal Plasma DNA Sequencing, Suggest Increased Risk of Feto-Placental Disease … … Extended Analysis Yields Results … Related Content … Sequencing all 24 human chromosomes uncovers rare disorders … …
News Release
Researchers and clinicians are sequencing human genomes faster than ever, so considering the societal implications of genomic data is even crucial.
… factors to consider. Now, researchers and clinicians are sequencing human genomes faster than ever, so considering the … of genomics research … Researchers and clinicians are sequencing human genomes faster than ever, so considering the … data and society, Lawrence Brody Ph.D., human genome sequencing, Reddit AMA … Researchers and clinicians are …
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.
… with input from clinical educators and administrators, The Method for Introducing a New Competency in Genomics (MINC) … to an online toolkit with more than 100 resources. ​ … Method for Introducing a New Competency in Genomics, MINC, …
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.
… and focus on applying new technologies, genome-sequencing strategies and analytical approaches. "This … genes each year using a technique called whole-exome sequencing. This method sequences all the regions of the genome responsible …
News Release
NIH will fund grants totaling $38 million over five years to develop methods that will improve the way that polygenic risk scores can be used to predict disease in diverse communities.
Fact Sheet
Early in the COVID-19 pandemic, researchers used state-of-the-art genomic sequencers to quickly sequence the SARS-CoV-2 virus.
… such as in a test tube) protocols to create mRNA in a method that mimics our own biological processes. First, they …
About Genomics
Resources for understanding the first complete, gapless sequence of a human genome.
… Credit: Ernesto Del Aguila III, NHGRI  Video: Fully sequencing the human genome Credit: Harry Wedel, NHGRI  …