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1.
Nucleic Acids Res ; 35(Database issue): D716-20, 2007 Jan.
Article in English | MEDLINE | ID: mdl-17151077

ABSTRACT

The variation resources within the University of California Santa Cruz Genome Browser include polymorphism data drawn from public collections and analyses of these data, along with their display in the context of other genomic annotations. Primary data from dbSNP is included for many organisms, with added information including genomic alleles and orthologous alleles for closely related organisms. Display filtering and coloring is available by variant type, functional class or other annotations. Annotation of potential errors is highlighted and a genomic alignment of the variant's flanking sequence is displayed. HapMap allele frequencies and linkage disequilibrium (LD) are available for each HapMap population, along with non-human primate alleles. The browsing and analysis tools, downloadable data files and links to documentation and other information can be found at http://genome.ucsc.edu/.


Subject(s)
Databases, Nucleic Acid , Polymorphism, Single Nucleotide , Alleles , Animals , Gene Frequency , Genomics , Genotype , Humans , Internet , Linkage Disequilibrium , Mice , Rats , Recombination, Genetic , Sequence Alignment , User-Computer Interface
2.
Nucleic Acids Res ; 35(Database issue): D663-7, 2007 Jan.
Article in English | MEDLINE | ID: mdl-17166863

ABSTRACT

The goal of the Encyclopedia Of DNA Elements (ENCODE) Project is to identify all functional elements in the human genome. The pilot phase is for comparison of existing methods and for the development of new methods to rigorously analyze a defined 1% of the human genome sequence. Experimental datasets are focused on the origin of replication, DNase I hypersensitivity, chromatin immunoprecipitation, promoter function, gene structure, pseudogenes, non-protein-coding RNAs, transcribed RNAs, multiple sequence alignment and evolutionarily constrained elements. The ENCODE project at UCSC website (http://genome.ucsc.edu/ENCODE) is the primary portal for the sequence-based data produced as part of the ENCODE project. In the pilot phase of the project, over 30 labs provided experimental results for a total of 56 browser tracks supported by 385 database tables. The site provides researchers with a number of tools that allow them to visualize and analyze the data as well as download data for local analyses. This paper describes the portal to the data, highlights the data that has been made available, and presents the tools that have been developed within the ENCODE project. Access to the data and types of interactive analysis that are possible are illustrated through supplemental examples.


Subject(s)
Databases, Nucleic Acid , Genome, Human , Genomics , Base Sequence , Humans , Internet , Sequence Alignment , Software , User-Computer Interface
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