{"id":179770,"date":"2022-04-16T19:57:45","date_gmt":"2022-04-16T14:27:45","guid":{"rendered":"https:\/\/blog.forumias.com\/?p=179770"},"modified":"2022-04-16T19:59:30","modified_gmt":"2022-04-16T14:29:30","slug":"humans-decoded","status":"publish","type":"post","link":"https:\/\/forumias.com\/blog\/humans-decoded\/","title":{"rendered":"Humans Decoded"},"content":{"rendered":"\n<h5><b>Context<\/b><span style=\"font-weight: 400;\">:\u00a0<\/span><\/h5>\n<p><span style=\"font-weight: 400;\">Scientists have completed the first full and seamless catalog of genetic instructions of humans. It&#8217;s expected that research will help to explain how every cell in a human body is created. It will help develop highly effective diagnostic tools and treatments for diseases.\u00a0<\/span><\/p>\n<h5><b>What is the background<\/b><span style=\"font-weight: 400;\">?<\/span><\/h5>\n<p><span style=\"font-weight: 400;\">Nobel Prize-winning Italian-American virologist Renato Dulbecco first pitched the idea to determine the DNA sequence of the entire human genome, way back in 1984.<\/span><\/p>\n<p><span style=\"font-weight: 400;\">An international research effort continued under the Human Genome Project.<\/span><\/p>\n<p><span style=\"font-weight: 400;\"><strong>Thirty-eight years and billions of dollars later<\/strong>, scientists completed the first full and seamless catalog of genetic instructions of humans. According to the Telomere-to-Telomere (T2T) consortium\u2019s collection of papers (recently published in Science), the sequence \u2014 comprising more than three billion base pairs across 23 chromosomes \u2014 is gapless.<\/span><\/p>\n<h5><b>What is DNA sequencing<\/b><span style=\"font-weight: 400;\">?<\/span><\/h5>\n<p><span style=\"font-weight: 400;\">Sequencing simply means determining the order of the base pairs in a segment of DNA. Human chromosomes range in size from about 50,000,000 to 300,000,000 base pairs (National Human Genome Research Institute, or NHGRI).<\/span><\/p>\n<h5><b>What led to the recent breakthrough?<\/b><\/h5>\n<p><span style=\"font-weight: 400;\">Over the past decade, two new DNA sequencing technologies emerged that can read longer sequences without compromising accuracy.\u00a0<\/span><\/p>\n<p><span style=\"font-weight: 400;\"><strong>1.)<\/strong> The <strong>PacBio HiFi DNA<\/strong> sequencing method can read about 20,000 letters with nearly perfect accuracy.\u00a0<\/span><\/p>\n<p><span style=\"font-weight: 400;\"><strong>2.)<\/strong> The <strong>Oxford Nanopore DNA sequencing method<\/strong> can read even more \u2014 up to 1 million DNA letters at a time \u2014 with modest accuracy. Both were used to generate the complete human genome sequence.<\/span><\/p>\n<h5><b>What is the significance of complete genomic sequencing<\/b><span style=\"font-weight: 400;\">?<\/span><\/h5>\n<p><span style=\"font-weight: 400;\">It shall help explain<\/span><b> how every cell in a human body is created, which <\/b><span style=\"font-weight: 400;\">may shed light on the treatment, prevention, and cure required for a disease. For instance, The Cancer Genome Atlas (TCGA), a cancer genomics program in the US, has already mapped genomic changes in 33 cancer types in order to improve cancer treatment.<\/span><\/p>\n<p><span style=\"font-weight: 400;\">It shall open the door for relatively <\/span><b>effective personalized or precision medicine<\/b><span style=\"font-weight: 400;\"> and genome editing in the future.<\/span><\/p>\n<p><span style=\"font-weight: 400;\">It should lead to powerful <\/span><b>preventive medication<\/b><span style=\"font-weight: 400;\"> and allow us to learn about risks of future illness, besides helping better plan dietary and lifestyle changes.<\/span><\/p>\n<p><span style=\"font-weight: 400;\">As DNA sequencing becomes the norm, it\u2019s likely that medical prescriptions will be based on our genes \u2014 minimizing side effects and making treatments relatively effective. Currently, there are already over 250 US FDA-approved drugs labeled with pharmacogenomic information that can be prescribed based on a patient\u2019s genetics.\u00a0<\/span><\/p>\n<h5><b>What is the way forward<\/b><span style=\"font-weight: 400;\">?<\/span><\/h5>\n<p><span style=\"font-weight: 400;\">The sequencing is done, but the work is far from over. Researchers now want to decode full sets of DNA from a larger pool of individuals <strong>to capture all the variations that exist in human DNA<\/strong>. Already researchers, in a separate project, are building a \u201chuman pangenome\u201d representing all the human genetic variations.<\/span><\/p>\n<p><span style=\"font-weight: 400;\">A <\/span><b>strong set of ethical guidelines encompassing genetic research and editing <\/b><span style=\"font-weight: 400;\">needs to be formulated. As gapless, human genome sequencing will enable society to select specific embryos to avoid health problems and may lead to the rise of \u201csuperhumans\u201d.<\/span><\/p>\n<p><b>Source<\/b><span style=\"font-weight: 400;\">: This post is created based on the article <strong>&#8220;Humans Decoded&#8221;<\/strong> published in <strong>Business Standard<\/strong> on <strong>16th April 2022<\/strong>.\u00a0<\/span><\/p>\n","protected":false},"excerpt":{"rendered":"<p>Context:\u00a0 Scientists have completed the first full and seamless catalog of genetic instructions of humans. It&#8217;s expected that research will help to explain how every cell in a human body is created. It will help develop highly effective diagnostic tools and treatments for diseases.\u00a0 What is the background? Nobel Prize-winning Italian-American virologist Renato Dulbecco first&hellip; <a class=\"more-link\" href=\"https:\/\/forumias.com\/blog\/humans-decoded\/\">Continue reading <span class=\"screen-reader-text\">Humans Decoded<\/span><\/a><\/p>\n","protected":false},"author":10322,"featured_media":0,"comment_status":"open","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"jetpack_post_was_ever_published":false,"footnotes":""},"categories":[1230,9],"tags":[10503,216],"class_list":["post-179770","post","type-post","status-publish","format-standard","hentry","category-9-pm-daily-articles","category-public","tag-business-standard","tag-gs-paper-3","entry"],"jetpack_featured_media_url":"","views":{"total":0,"cached_at":1700772366,"cached_date":1702907088},"jetpack_sharing_enabled":true,"_links":{"self":[{"href":"https:\/\/forumias.com\/blog\/wp-json\/wp\/v2\/posts\/179770","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/forumias.com\/blog\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/forumias.com\/blog\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/forumias.com\/blog\/wp-json\/wp\/v2\/users\/10322"}],"replies":[{"embeddable":true,"href":"https:\/\/forumias.com\/blog\/wp-json\/wp\/v2\/comments?post=179770"}],"version-history":[{"count":0,"href":"https:\/\/forumias.com\/blog\/wp-json\/wp\/v2\/posts\/179770\/revisions"}],"wp:attachment":[{"href":"https:\/\/forumias.com\/blog\/wp-json\/wp\/v2\/media?parent=179770"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/forumias.com\/blog\/wp-json\/wp\/v2\/categories?post=179770"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/forumias.com\/blog\/wp-json\/wp\/v2\/tags?post=179770"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}