{"id":52567,"date":"2015-01-13T16:47:41","date_gmt":"2015-01-13T21:47:41","guid":{"rendered":"http:\/\/www.euvolution.com\/prometheism-transhumanism-posthumanism\/uc-santa-cruz-to-lead-effort-to-build-a-new-map-of-human-genetic-variation\/"},"modified":"2015-01-13T16:47:41","modified_gmt":"2015-01-13T21:47:41","slug":"uc-santa-cruz-to-lead-effort-to-build-a-new-map-of-human-genetic-variation","status":"publish","type":"post","link":"https:\/\/www.euvolution.com\/prometheism-transhumanism-posthumanism\/transhuman-news-blog\/genome\/uc-santa-cruz-to-lead-effort-to-build-a-new-map-of-human-genetic-variation\/","title":{"rendered":"UC Santa Cruz to lead effort to build a new map of human genetic variation"},"content":{"rendered":"<p><p>  Simons Foundation awards up to $1 million to UC Santa Cruz  Genomics Institute to develop a comprehensive Human Genome  Variation Map for scientific and medical research<\/p>\n<p>  VIDEO:Benedict Paten discusses work on the  Human Genome Variation Map at the University of California Santa  Cruz Genomics Institute. view  more<\/p>\n<p>    Researchers at the UC Santa Cruz Genomics Institute have    received a grant for up to $1 million from the Simons    Foundation to develop a comprehensive map of human genetic    variation. The Human Genome Variation Map will be a critical    new resource for both medical research and basic research in    the life sciences.  <\/p>\n<p>    The one-year pilot project aims to overcome the limitations of    the current model for analyzing human genome data, which is    based on the use of a single reference sequence for the human    genome. Essentially, all novel sequencing data is analyzed by    mapping new genome sequences to this one reference set of 24    human chromosomes to identify variants. But this approach leads    to biases and mapping ambiguities, and some variants simply    cannot be described with respect to the reference genome,    according to David Haussler, professor of biomolecular    engineering and director of the Genomics Institute at UC Santa    Cruz.  <\/p>\n<p>    \"One exemplary human genome cannot represent humanity as a    whole, and the scientific community has not been able to agree    on a single precise method to refer to and represent human    genome variants. There is a great deal we still don't know    about human genetic variation because of these problems,\" said    Haussler, who will lead the project with co-investigator    Benedict Paten, a research scientist at the Genomics Institute.  <\/p>\n<p>    According to Paten, the proliferation of different genomic    databases has resulted in hundreds of specialized coordinate    systems and nomenclatures for describing human genetic    variation. UC Santa Cruz genomics researchers are intimately    familiar with this \"Tower of Babel\" of databases through their    work to display data from all these sources on the widely used    UCSC Genome Browser. Launched in July 2000 shortly after UC    Santa Cruz posted the first working draft of the human genome    sequence on the Internet, the browser now serves 130,000    researchers around the world and gets more than 1 million web    page requests per day.  <\/p>\n<p>    \"For now, all our browser staff can do is to serve the data    from these disparate sources in their native, mutually    incompatible formats,\" Paten said. \"This lack of comprehensive    integration, coupled with the over-simplicity of the reference    model, seriously impedes progress in the science of genomics    and its use in medicine.\"  <\/p>\n<p>    Recently, with funding from the Simons Foundation, researchers    David Reich and Nick Patterson at the Broad Institute of MIT    and Harvard have amassed more than 300 complete human genome    sequences representing a range of ethnicities. Haussler and    Paten plan to use this set of human genomes, which they say is    deeper and more completely organized than any prior human data    set, to build a new graph-based human reference genome    structure.  <\/p>\n<p>    \"This unique data set of genome diversity gives us an    opportunity to define a comprehensive reference genome    structure that can be truly representative of human variation.    Eventually, we will want to expand it to include many more    genomes, but this pilot project will focus on building a map    structure based on the Reich-Patterson data set,\" Paten said.  <\/p>\n<p>    The new Human Genome Variation Map will replace the current    snarl of isolated, incompatible databases of human genetic    variation with a single, fundamental representation formalized    as a very large mathematical graph. The clean mathematical    formulation is a major strength of this new approach, Paten    said.  <\/p>\n<p><!-- Auto Generated --><\/p>\n<p>Visit link:<br \/>\n<a target=\"_blank\" href=\"http:\/\/www.eurekalert.org\/pub_releases\/2015-01\/uoc--usc011315.php\/RK=0\/RS=hXlmnHWE83zlbw3c_Nx6GUpTcpg-\" title=\"UC Santa Cruz to lead effort to build a new map of human genetic variation\">UC Santa Cruz to lead effort to build a new map of human genetic variation<\/a><\/p>\n","protected":false},"excerpt":{"rendered":"<p> Simons Foundation awards up to $1 million to UC Santa Cruz Genomics Institute to develop a comprehensive Human Genome Variation Map for scientific and medical research VIDEO:Benedict Paten discusses work on the Human Genome Variation Map at the University of California Santa Cruz Genomics Institute. view more Researchers at the UC Santa Cruz Genomics Institute have received a grant for up to $1 million from the Simons Foundation to develop a comprehensive map of human genetic variation. The Human Genome Variation Map will be a critical new resource for both medical research and basic research in the life sciences.  <a href=\"https:\/\/www.euvolution.com\/prometheism-transhumanism-posthumanism\/transhuman-news-blog\/genome\/uc-santa-cruz-to-lead-effort-to-build-a-new-map-of-human-genetic-variation\/\">Continue reading <span class=\"meta-nav\">&rarr;<\/span><\/a><\/p>\n","protected":false},"author":1,"featured_media":0,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[25],"tags":[],"class_list":["post-52567","post","type-post","status-publish","format-standard","hentry","category-genome"],"_links":{"self":[{"href":"https:\/\/www.euvolution.com\/prometheism-transhumanism-posthumanism\/wp-json\/wp\/v2\/posts\/52567"}],"collection":[{"href":"https:\/\/www.euvolution.com\/prometheism-transhumanism-posthumanism\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/www.euvolution.com\/prometheism-transhumanism-posthumanism\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/www.euvolution.com\/prometheism-transhumanism-posthumanism\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"https:\/\/www.euvolution.com\/prometheism-transhumanism-posthumanism\/wp-json\/wp\/v2\/comments?post=52567"}],"version-history":[{"count":0,"href":"https:\/\/www.euvolution.com\/prometheism-transhumanism-posthumanism\/wp-json\/wp\/v2\/posts\/52567\/revisions"}],"wp:attachment":[{"href":"https:\/\/www.euvolution.com\/prometheism-transhumanism-posthumanism\/wp-json\/wp\/v2\/media?parent=52567"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/www.euvolution.com\/prometheism-transhumanism-posthumanism\/wp-json\/wp\/v2\/categories?post=52567"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/www.euvolution.com\/prometheism-transhumanism-posthumanism\/wp-json\/wp\/v2\/tags?post=52567"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}