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  2. 1000 Genomes Project - Wikipedia

    en.wikipedia.org/wiki/1000_Genomes_Project

    1000 Genomes Project. The 1000 Genomes Project (1KGP), taken place from January 2008 to 2015, was an international research effort to establish the most detailed catalogue of human genetic variation at the time. Scientists planned to sequence the genomes of at least one thousand anonymous healthy participants from a number of different ethnic ...

  3. 1000 Plant Genomes Project - Wikipedia

    en.wikipedia.org/wiki/1000_Plant_Genomes_Project

    The 1000 Plant Transcriptomes Initiative (1KP) was an international research effort to establish the most detailed catalogue of genetic variation in plants. It was announced in 2008 and headed by Gane Ka-Shu Wong and Michael Deyholos of the University of Alberta. The project successfully sequenced the transcriptomes (expressed genes) of 1000 ...

  4. Wellcome Sanger Institute - Wikipedia

    en.wikipedia.org/wiki/Wellcome_Sanger_Institute

    Hinxton. , Cambridgeshire, United Kingdom. Coordinates. 52°04′39″N 00°11′15″E  /  52.07750°N 0.18750°E  / 52.07750; 0.18750. Website. sanger.ac.uk. The Wellcome Sanger Institute, previously known as The Sanger Centre and Wellcome Trust Sanger Institute, is a non-profit British genomics and genetics research institute ...

  5. Imputation (genetics) - Wikipedia

    en.wikipedia.org/wiki/Imputation_(genetics)

    In genetics, imputation is the statistical inference of unobserved genotypes. [1] It is achieved by using known haplotypes in a population, for instance from the HapMap or the 1000 Genomes Project in humans, thereby allowing to test for association between a trait of interest (e.g. a disease) and experimentally untyped genetic variants, but whose genotypes have been statistically inferred ...

  6. Wellcome Centre for Human Genetics - Wikipedia

    en.wikipedia.org/wiki/Wellcome_Centre_for_Human...

    Coordinates. 51°45′08″N 1°12′55″W  /  51.752248°N 1.215255°W  / 51.752248; -1.215255. Website. www.well.ox.ac.uk. The Wellcome Centre for Human Genetics is a human genetics research centre of the Nuffield Department of Medicine in the Medical Sciences Division, University of Oxford, funded by the Wellcome Trust among others ...

  7. UCSC Genome Browser - Wikipedia

    en.wikipedia.org/wiki/UCSC_Genome_Browser

    For example, the entire contents of each release of the dbSNP database from NCBI are mapped to human, mouse and other genomes. This includes the fruits of the 1000 Genomes Project, as soon as they are released in dbSNP. Other types of variation data include copy-number variation data and human population allele frequencies from the HapMap project.