{"id":188690,"date":"2017-04-21T02:01:39","date_gmt":"2017-04-21T06:01:39","guid":{"rendered":"https:\/\/www.euvolution.com\/prometheism-transhumanism-posthumanism\/congenica-and-edico-genome-partner-to-speed-analysis-from-dna-pr-newswire-press-release\/"},"modified":"2017-04-21T02:01:39","modified_gmt":"2017-04-21T06:01:39","slug":"congenica-and-edico-genome-partner-to-speed-analysis-from-dna-pr-newswire-press-release","status":"publish","type":"post","link":"https:\/\/www.euvolution.com\/prometheism-transhumanism-posthumanism\/transhuman-news-blog\/genome\/congenica-and-edico-genome-partner-to-speed-analysis-from-dna-pr-newswire-press-release\/","title":{"rendered":"Congenica and Edico Genome Partner to Speed Analysis from &#8216;DNA &#8230; &#8211; PR Newswire (press release)"},"content":{"rendered":"<p><p>    Thomas    Weaver, Ph.D., Chief Executive Officer of    Congenica, said: \"Sapientia is already used extensively    throughout the NHS in the UK as well as by clinical scientists    providing reports for the 100,000 Genomes Project. Without a    diagnosis, it is difficult to select the most appropriate    treatment plan for a patient or make a prognosis of what the    likely outcomes may be. Edico shares our vision of transforming    healthcare by developing easy to use, highly automated genomics    analysis solutions, and by combining our complementary    technologies we aim to accelerate the clinician's ability to    use genomics to diagnose a patients' disease, and make this    available on a global basis.\"   <\/p>\n<p>    Edico's DRAGEN Bio-IT processor has been assessed as part of    University College London's (UCL) Rapid Paediatric Sequencing    Project (RaPs), a pilot aimed at evaluating the use of rapid    whole genome sequencing (WGS) for rare diseases in an intensive    care clinical setting.  <\/p>\n<p>    Phil    Beales, Professor of Medical and Molecular    Genetics at UCL, said: \"For children with rare diseases    and their parents, answers cannot come quickly enough. Faster    answers mean less time finding a diagnosis and more time making    decisions about treatment and care. After extensively testing    and validating the platforms, we were impressed by the speed,    accuracy and cost savings conferred. Initially, we will apply    the technology to a number of clinical cases where rapid    turnaround is especially critical, and ultimately envisage the    solution will be widely used as we scale our efforts.\"  <\/p>\n<p>    Added Pieter van    Rooyen, Ph.D., Chief Executive Officer of Edico    Genome: \"As genomics marches towards the clinic, we recognize    clinicians and researchers need easy to use, all-in-one    solutions that enable genomic data to be analysed and shared    quickly, easily, accurately and cost effectively. Congenica has    first-hand perspective of the needs of the clinical genomics    community from its extensive work with the NHS, including the    Genomics England initiative, and through this new collaboration    we're able to create an all-in-one, easy-to-use offering that    significantly accelerates the ability of hospitals and clinical    labs to move from the sequencing of a sample to a clinical    diagnosis.\"  <\/p>\n<p>    About Congenica  <\/p>\n<p>    Rapid, accurate and scalable diagnosis of patients with    inherited genetic diseases helps accelerate access to the best    clinical treatments and prevention strategies. Congenica, a    global clinical genetics software company, created Sapientia    that offers Clinical Scientists, Hospitals and Clinical Labs an    all in one software platform to enable scalable, accurate, fast    and flexible genetic diagnostic services. Congenica is a    global company, headquartered in Cambridge UK and founded    by pioneering researchers from the Sanger Institute.  <\/p>\n<p>    Clinicians and scientists are using Sapientia, a cloud-based    integrated software platform to analyze and interpret genetic    data linked to patients' phenotypes. The software is designed    to support clinical interpretation workflows and generate    professional diagnostic reports. Sapientia handles the main    data inputs including BAM, VCF and FASTQ files in many upload    formats and the added flexibility to Integrate and manage    customer legacy data to enhance diagnostic capabilities.  <\/p>\n<p>    Find out more about Congenica at <a href=\"http:\/\/www.congenica.com\" rel=\"nofollow\">http:\/\/www.congenica.com<\/a> or    follow @Congenica.  <\/p>\n<p>    About Sapientia  <\/p>\n<p>    Sapientia facilitates analysis of genetic data to produce a    comprehensive diagnostic report that can be linked to patients'    symptoms, supporting clinical decision-making about rare    genetic disease. The platform is based on pioneering research    from the UK Wellcome Trust Sanger Institute, NHS clinicians and    regional genetic testing laboratories, and its underlying    technology has been validated by leading independent institutes    and clinicians, including Genomics England Ltd.  <\/p>\n<p>    About Edico Genome  <\/p>\n<p>    The use of next-generation sequencing is growing at an    unprecedented pace, creating a need for easy to implement    infrastructure that enables rapid, accurate and cost-effective    processing and storage of this big data. Edico Genome has    created a patented, end-to-end    platform solution for analysis of next-generation sequencing    data, DRAGEN, which speeds whole    genome data analysis from hours to minutes while maintaining    high accuracy and reducing costs. Top clinicians and researchers are    utilizing the platform to achieve faster diagnoses for    critically ill newborns, cancer patients and expecting parents    waiting on prenatal tests, and faster results for scientists    and drug developers.  <\/p>\n<p>    For more information, visit <a href=\"http:\/\/www.EdicoGenome.com\" rel=\"nofollow\">http:\/\/www.EdicoGenome.com<\/a>    or follow @EdicoGenome.  <\/p>\n<p>    About DRAGEN  <\/p>\n<p>    The DRAGEN platform features optimized algorithms for mapping,    alignment, sorting, variant calling and more. Multiple    end-to-end, clinical-grade pipelines are available from Edico,    including genome\/exome, cancer, transcriptome\/RNA-seq,    structural variant, copy number variant, epigenome\/methyl-seq,    metagenome\/microbiome, joint genotyping and third-party    pipelines such as GATK 3.6. The platform is flexible and allows    for customization of algorithms and existing pipelines.    Best-in-class solutions for onsite, cloud or hybrid cloud    analysis have been created through partnerships with top    technology companies, includingIntel,IBM,Dell EMC, andAmazon Web Services.  <\/p>\n<\/p>\n<p>    To view the original version on PR Newswire, visit:<a href=\"http:\/\/www.prnewswire.com\/news-releases\/congenica-and-edico-genome-partner-to-speed-analysis-from-dna-to-diagnosis-for-inherited-diseases-300442461.html\" rel=\"nofollow\">http:\/\/www.prnewswire.com\/news-releases\/congenica-and-edico-genome-partner-to-speed-analysis-from-dna-to-diagnosis-for-inherited-diseases-300442461.html<\/a>  <\/p>\n<p>    SOURCE Edico Genome  <\/p>\n<p>    <a href=\"http:\/\/www.edicogenome.com\" rel=\"nofollow\">http:\/\/www.edicogenome.com<\/a><\/p>\n<p><!-- Auto Generated --><\/p>\n<p>Originally posted here:<br \/>\n<a target=\"_blank\" href=\"http:\/\/www.prnewswire.com\/news-releases\/congenica-and-edico-genome-partner-to-speed-analysis-from-dna-to-diagnosis-for-inherited-diseases-300442461.html\" title=\"Congenica and Edico Genome Partner to Speed Analysis from 'DNA ... - PR Newswire (press release)\">Congenica and Edico Genome Partner to Speed Analysis from 'DNA ... - PR Newswire (press release)<\/a><\/p>\n","protected":false},"excerpt":{"rendered":"<p> Thomas Weaver, Ph.D., Chief Executive Officer of Congenica, said: \"Sapientia is already used extensively throughout the NHS in the UK as well as by clinical scientists providing reports for the 100,000 Genomes Project. Without a diagnosis, it is difficult to select the most appropriate treatment plan for a patient or make a prognosis of what the likely outcomes may be.  <a href=\"https:\/\/www.euvolution.com\/prometheism-transhumanism-posthumanism\/transhuman-news-blog\/genome\/congenica-and-edico-genome-partner-to-speed-analysis-from-dna-pr-newswire-press-release\/\">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-188690","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\/188690"}],"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=188690"}],"version-history":[{"count":0,"href":"https:\/\/www.euvolution.com\/prometheism-transhumanism-posthumanism\/wp-json\/wp\/v2\/posts\/188690\/revisions"}],"wp:attachment":[{"href":"https:\/\/www.euvolution.com\/prometheism-transhumanism-posthumanism\/wp-json\/wp\/v2\/media?parent=188690"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/www.euvolution.com\/prometheism-transhumanism-posthumanism\/wp-json\/wp\/v2\/categories?post=188690"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/www.euvolution.com\/prometheism-transhumanism-posthumanism\/wp-json\/wp\/v2\/tags?post=188690"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}