{"id":63104,"date":"2015-03-26T10:47:24","date_gmt":"2015-03-26T14:47:24","guid":{"rendered":"http:\/\/www.euvolution.com\/prometheism-transhumanism-posthumanism\/icelands-giant-genome-project-points-to-future-of-medicine\/"},"modified":"2015-03-26T10:47:24","modified_gmt":"2015-03-26T14:47:24","slug":"icelands-giant-genome-project-points-to-future-of-medicine","status":"publish","type":"post","link":"https:\/\/www.euvolution.com\/prometheism-transhumanism-posthumanism\/transhuman-news-blog\/genome\/icelands-giant-genome-project-points-to-future-of-medicine\/","title":{"rendered":"Iceland&#39;s Giant Genome Project Points to Future of Medicine"},"content":{"rendered":"<p><p>  Photo: Chris Lund The blood of a thousand Icelanders.<\/p>\n<p>    When the first Viking explorers began settling Iceland, none    could have imagined that theirdescendants would pioneer    thefuture of modern medicine by surveying the human    genome. Fast forward 1000 years to today,    whenanIcelandic company has revealedits    success insequencing the largest-ever set of human    genomes from a single population. The new wealth of genetic    data has already begunchanging our understanding of    human evolutionary history. It also sets the stage for a new    era of preventive medicinebased on individual genetic    risks fordiseases such as cancer and    Alzheimers disease.  <\/p>\n<p>    Themilestone in genome sequencing    comesfromdeCODE Genetics, a biopharmaceutical    company inReykjavk, Iceland. Theirwork, published    as four papers in the 25 March 2015 issue of the     journalNature Genetics,has yielded new    insights aboutthecommon human ancestor for the        male Y chromosomenarrowed tosomewhere between    174,000 and 321,000 years agobased on their latest calculation    of human mutation rates. Another part of their work discovered    thatabout 7.7 percent of the modern-day population has        rare knockout genesgenes that have beendisabled by    mutations. Early research has also revealed a     mutation in theABCA7gene,whichdoubles    the risk of Alzheimers disease in Iceland and other    populations dominated by European ancestry.  <\/p>\n<p>    These are just a handful of observations    that have come out of the ability to look at the sequence of    the genome of an entire    nation,saidKari Stefansson, founder    of deCODE Genetics, during a press briefing onMonday, 23    March.What is more, we are now    sitting in Iceland with the possibility of taking advantage of    these insights when it comes to the Icelandic healthcare    system.  <\/p>\n<p>    The company sequenced thewhole genomes of    2636 Icelanders and used those genomes as the basis for    calculatingthe genetic variances for the entire Icelandic    population.Iceland represents a unique laboratory    for genetics researchers because much of the modern population    traces its lineage to a relatively small number of founders; a    fact that makes it easier to trace genealogies and    pedigrees.  <\/p>\n<p>    Myles Axton, chief editor ofNature Genetics,    introduced the Monday press briefingbydescribing    how the genetic sequencing strategy in Iceland could also work    for other countries:  <\/p>\n<p>      This strategy of sequencing the DNA of about 1 in 100 of the      population, a total of 2,636 Icelanders, and then using      shared sets of common genetic variance to predict the full      spectrum of genetic variance carried by the whole population,      is a great model for the future of human genetics. This      technique can be applied to any population and is all the      more accurate when there are pedigrees available for much of      the population.    <\/p>\n<p>    Genome sequencing has alloweddeCODE Genetics to begin    data-mining information about how certain genes function and    their relationship to a broad array of diseases. Past findings    from such research included additional insights about gene    variants associated with Alzheimers disease and schizophrenia.  <\/p>\n<p>    The growing database on knockout genes may prove particularly    helpful when matched against the phenotypes of    individualsthe physical traits or characteristics that    can be observed. Perhaps unsurprisingly, the researchers found    that knockouts are least common among genes expressed in the    brain, given that organs importance.  <\/p>\n<p>    Basically what we hope to get out of phenotyping the carriers    of these knockouts is to figure out which biochemical pathways    are necessary for which physiological functions, Stefansson    explained.Then the question is whetherthere is    redundancy in some of these physiological functions;are    there alternative biochemical pathways that can compensate for    the loss of one?  <\/p>\n<p><!-- Auto Generated --><\/p>\n<p>Original post:<br \/>\n<a target=\"_blank\" href=\"http:\/\/spectrum.ieee.org\/tech-talk\/biomedical\/diagnostics\/icelands-giant-genome-project-shows-future-medicine\/RK=0\/RS=N7HdKMkimlmk9xc1mzhevszIwm4-\" title=\"Iceland&#39;s Giant Genome Project Points to Future of Medicine\">Iceland&#39;s Giant Genome Project Points to Future of Medicine<\/a><\/p>\n","protected":false},"excerpt":{"rendered":"<p> Photo: Chris Lund The blood of a thousand Icelanders. When the first Viking explorers began settling Iceland, none could have imagined that theirdescendants would pioneer thefuture of modern medicine by surveying the human genome. Fast forward 1000 years to today, whenanIcelandic company has revealedits success insequencing the largest-ever set of human genomes from a single population.  <a href=\"https:\/\/www.euvolution.com\/prometheism-transhumanism-posthumanism\/transhuman-news-blog\/genome\/icelands-giant-genome-project-points-to-future-of-medicine\/\">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-63104","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\/63104"}],"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=63104"}],"version-history":[{"count":0,"href":"https:\/\/www.euvolution.com\/prometheism-transhumanism-posthumanism\/wp-json\/wp\/v2\/posts\/63104\/revisions"}],"wp:attachment":[{"href":"https:\/\/www.euvolution.com\/prometheism-transhumanism-posthumanism\/wp-json\/wp\/v2\/media?parent=63104"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/www.euvolution.com\/prometheism-transhumanism-posthumanism\/wp-json\/wp\/v2\/categories?post=63104"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/www.euvolution.com\/prometheism-transhumanism-posthumanism\/wp-json\/wp\/v2\/tags?post=63104"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}