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News Release
The goat has contributed its DNA to a new method for high-quality, low-cost genome reconstruction, one that will be useful for reading human and other genomes.
… 10,000 years ago. Now, the goat has contributed its DNA to a study that presents a new method for high-quality, … genomes. They cannot be sequenced from end to end in a single step. Instead, DNA must first be broken into smaller … researchers used a variety of methods, including PacBio sequencing , which was released in 2011. Dr. Phillippy and …
News Release
April 25, 2023 marks the 20th anniversary of the completion of the Human Genome Project and the 70th anniversary of the discovery of DNA’s double-helical structure, milestones being celebrated as part of National DNA Day.
… National DNA Day commemorates Human Genome Project’s completion and discovery of DNA’s double-helical structure. … Today marks the 20th … Project and the 70th anniversary of the discovery of DNA’s double-helical structure, milestones being celebrated …
Staff
Dr. Mullikin was the former director of the NIH Intramural Sequencing Center (NISC).
… to analyze large data sets generated by systematic DNA sequencing projects. A highly skilled computational … group assembled the genome of Plasmodium coatneyi from a single lane of HiSeq2000 data, which provided more than … J, Henderson DK, Frank KM, Palmore TN, Segre JA. Single-molecule sequencing to track plasmid diversity of …
Educational Resources
Restriction fragment length polymorphism (RFLP) is a type of polymorphism that results from variation in the DNA sequence recognized by restriction enzymes.
… a type of polymorphism that results from variation in the DNA sequence recognized by restriction enzymes. … Deoxyribonucleic Acid (DNA), Electrophoresis, Genetic Marker, Polymorphism, … to differences (or variations) among people in their DNA sequences at sites recognized by restriction enzymes. …
Infographic
An infographic that explains why it was so difficult to fully complete the human genome sequence.
… to me." … The human genome contains a massive amount of DNA. The human genome consists of about 3 billion bases in a … must first determine the sequence of random pieces of DNA and then use those smaller sequences to put the whole … with a vision. Even with new technologies, genome sequencing is still tough, time-consuming work that requires …
News Release
The Telomere-to-Telomere (T2T) Consortium has generated the first truly complete sequence of a human Y chromosome - the final human chromosome to be fully sequenced.
… of two specific repeating sequences known as satellite DNA. It makes a beautiful, quilt-like pattern. All … sequence particularly difficult to complete. Assembling sequencing data is like trying to read a long book cut into … pieces of the human genome, the T2T Consortium applied new DNA sequencing technologies and sequence assembly methods, as …
Research Funding
GS-IT provides sequence analysis tools and software to scientists who rely on genomics in their research.
… … Grantees … Program Staff … Related Content … Genome Sequencing Informatics Tools (GS-IT) provides "researcher … biological, biomedical and clinical research. … Genome Sequencing Informatics Tools … Genome Sequencing Informatics Tools … GS-IT provides sequence …
News Release
NIH will support research that incorporates DNA sequence information into electronic medical records.
… of Health will support research that incorporates DNA sequence information into electronic medical records. The … of rare genomic variants (inherited differences in the DNA code) in about 100 clinically relevant genes. The … variants with clinical implications by using the latest sequencing technologies to examine rare and common variants …
Educational Resources
Pharmacogenomics is a branch of pharmacology concerned with using DNA and amino acid sequence data to inform drug development and testing.
… is a branch of pharmacology concerned with using DNA and amino acid sequence data to inform drug development … and testing. … Amino Acids, Deoxyribonucleic Acid (DNA), Genetic Variation, Haplotype, Single Nucleotide Polymorphisms (SNPs), Personalized Medicine …
Research Funding
A collaborative large-scale genome sequencing effort to identify rare risk and protective variants contributing to multiple common disease phenotypes.
… Genomics (CCDG) are a collaborative large-scale genome sequencing effort to comprehensively identify rare risk and … Gene Variants, Genetic Risk, Common Disease, Rare Disease, Dna Sequencing, Dna Sequencing Technology … A collaborative large-scale …