{"id":42189,"date":"2018-02-26T11:08:35","date_gmt":"2018-02-26T11:08:35","guid":{"rendered":"https:\/\/sistemasgenomicos.digitis.net\/specialists\/precision-diagnosis\/postnatal-stage\/sg-oncobytes\/point-mutation-digital-pcr\/"},"modified":"2018-02-27T15:49:38","modified_gmt":"2018-02-27T15:49:38","slug":"point-mutation-digital-pcr","status":"publish","type":"page","link":"https:\/\/sistemasgenomicos.com\/en\/specialists\/precision-diagnosis\/postnatal-stage\/sg-oncobytes\/point-mutation-digital-pcr\/","title":{"rendered":"&#8211; Point Mutation digital PCR"},"content":{"rendered":"\n  <div class=\"banner has-hover\" id=\"banner-975712982\">\n          <div class=\"banner-inner fill\">\n        <div class=\"banner-bg fill\" >\n            <div class=\"bg fill bg-fill \"><\/div>\n                        <div class=\"overlay\"><\/div>            \n                    <\/div>\n\t\t\n        <div class=\"banner-layers container\">\n            <div class=\"fill banner-link\"><\/div>      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class=\"nav-wrapper\"><ul class=\"nav nav-uppercase nav-vertical nav-simple text-left nav-left\"><p class=\"lead shortcode-error text-center\">Sorry, no pages was found<\/p><\/ul><\/div>\n\t\t<\/div>\n\t\t\t\t\n<style>\n#col-486452454 > .col-inner {\n  padding: 10px 10px 10px 10px;\n}\n<\/style>\n\t<\/div>\n\n\t\n\n\t<div id=\"col-1963462704\" class=\"col medium-9 small-12 large-9\"  >\n\t\t\t\t<div class=\"col-inner\"  >\n\t\t\t\n\t\t\t\n<div class=\"row row-dashed\"  id=\"row-570326954\">\n\n\t<div id=\"col-1073218133\" class=\"col medium-6 small-12 large-6\"  >\n\t\t\t\t<div class=\"col-inner text-left\"  >\n\t\t\t\n\t\t\t\n\n\t\t<div class=\"icon-box featured-box icon-box-left text-left\"  >\n\t\t\t\t\t<div class=\"icon-box-img\" style=\"width: 98px\">\n\t\t\t\t<div class=\"icon\">\n\t\t\t\t\t<div class=\"icon-inner\" >\n\t\t\t\t\t\t<img loading=\"lazy\" decoding=\"async\" width=\"300\" height=\"260\" src=\"https:\/\/sistemasgenomicos.com\/wp-content\/uploads\/2017\/11\/pruebas-geneticas-1-300x260.png\" class=\"attachment-medium size-medium\" alt=\"\" srcset=\"https:\/\/sistemasgenomicos.com\/wp-content\/uploads\/2017\/11\/pruebas-geneticas-1-300x260.png 300w, https:\/\/sistemasgenomicos.com\/wp-content\/uploads\/2017\/11\/pruebas-geneticas-1-209x181.png 209w, https:\/\/sistemasgenomicos.com\/wp-content\/uploads\/2017\/11\/pruebas-geneticas-1-418x363.png 418w, https:\/\/sistemasgenomicos.com\/wp-content\/uploads\/2017\/11\/pruebas-geneticas-1.png 524w\" sizes=\"auto, (max-width: 300px) 100vw, 300px\" \/>\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t<\/div>\n\t\t\t\t<div class=\"icon-box-text last-reset\">\n\t\t\t\t\t\t\t\t\t\n<h3>Point mutation digital PCR<\/h3>\n<p>Sistemas Gen\u00f3micos uses the next-generation <em>droplet digital PCR (ddPCR)<\/em> technique to locate mutations associated with different tumour diseases.<\/p>\n\t\t<\/div>\n\t<\/div>\n\t\n\t\n\t\t<\/div>\n\t\t\t\t\t<\/div>\n\n\t\n\n\t<div id=\"col-1305497172\" class=\"col medium-6 small-12 large-6\"  >\n\t\t\t\t<div class=\"col-inner text-left\"  >\n\t\t\t\n\t\t\t\n<p>With this technique, our laboratories detect early on with a high level of precision and sensitivity, with the ability to quantify variants present at low frequency:<\/p>\n<ul>\n<li class=\"bullet-arrow\">75% (<em>NRAS<\/em>), 60% (<em>KRAS<\/em>) and 80% (<em>BRAF<\/em>) of mutations associated with bowel cancer<\/li>\n<li class=\"bullet-arrow\">90% (<em>EGFR<\/em>) of mutations associated with lung cancer<\/li>\n<li class=\"bullet-arrow\">80% (<em>BRAF<\/em>) of mutations associated with Melanoma<\/li>\n<\/ul>\n\t\t<\/div>\n\t\t\t\t\n<style>\n#col-1305497172 > .col-inner {\n  margin: 0px 0px 0px 0px;\n}\n<\/style>\n\t<\/div>\n\n\t\n<\/div>\n\t\t<\/div>\n\t\t\t\t\t<\/div>\n\n\t\n<\/div>\n\t<section class=\"section\" id=\"section_509939829\">\n\t\t<div class=\"bg section-bg fill bg-fill  bg-loaded\" >\n\n\t\t\t\n\t\t\t<div class=\"section-bg-overlay absolute fill\"><\/div>\n\t\t\t\n\n\t\t<\/div>\n\n\t\t\n\n\t\t<div class=\"section-content relative\">\n\t\t\t\n<div class=\"container section-title-container\" ><h3 class=\"section-title section-title-center\"><b><\/b><span class=\"section-title-main\" >Clinical Applications<\/span><b><\/b><\/h3><\/div>\n<div class=\"row\"  id=\"row-1849296172\">\n\n\t<div id=\"col-700058084\" class=\"col small-12 large-12\"  >\n\t\t\t\t<div class=\"col-inner\"  >\n\t\t\t\n\t\t\t\n<ul>\n<li class=\"bullet-checkmark\"><span style=\"font-size: 120%;\">Detection and quantification of the most common variants in samples in paraffin of somatic tumours (lung, melanoma and bowel), relevant for the selection of the right pharmaceuticals for the patient at the initial time of diagnosis.<\/span><\/li>\n<li class=\"bullet-checkmark\"><span style=\"font-size: 120%;\">Monitoring of the state of remission of the tumour using the regular detection of the variant identified at the time of diagnosis, using samples in paraffin.<\/span><\/li>\n<\/ul>\n\t\t<\/div>\n\t\t\t\t\t<\/div>\n\n\t\n<\/div>\n\t\t<\/div>\n\n\t\t\n<style>\n#section_509939829 {\n  padding-top: 30px;\n  padding-bottom: 30px;\n}\n#section_509939829 .section-bg-overlay {\n  background-color: rgba(54, 97, 159, 0.1);\n}\n<\/style>\n\t<\/section>\n\t\n<div class=\"container section-title-container\" style=\"margin-top:30px;\"><h3 class=\"section-title section-title-center\"><b><\/b><span class=\"section-title-main\" >Lorem ipsum dolor sit amet...<\/span><b><\/b><\/h3><\/div>\n<div class=\"row\"  id=\"row-745492677\">\n\n\t<div id=\"col-684268340\" class=\"col small-12 large-12\"  >\n\t\t\t\t<div class=\"col-inner\"  >\n\t\t\t\n\t\t\t\n<p>The technique is based on clonal amplification using PCR on a part of the sample. The system divides the samples of nucleic acids into up to 20,000 drops and each of them will have a maximum of one template DNA molecule. Each drip will act as an individual container for the amplification reaction. Then, the system transforms the analogue signal received into a digital signal depending of presence or absence. Lastly, the result is shown as a percentage or <em>ratio<\/em> of DNA carrying the variant under study compared to the <em>wild type<\/em> DNA.<\/p>\n<ul>\n<li class=\"bullet-checkmark\"><strong>Simplicity<\/strong>: simplification of the absolute quantification of the copies of DNA carrying  the variant under study.<\/li>\n<li class=\"bullet-checkmark\"><strong>Precision<\/strong>: the division of the drops in the sample allows us to quantify the tiny difference between the numbers of copies in the target DNA sequence.<\/li>\n<li class=\"bullet-checkmark\"><strong>Sensitivity<\/strong>: increases the signal\/noise ratio thanks to the enrichment of template DNA molecules against the <em>background<\/em> DNA; this way we get heightened sensitivity in the detection of low-frequency sequences (\u00b110%).<\/li>\n<li class=\"bullet-checkmark\"><strong>Resistance to inhibitors<\/strong>: allows us to work with environmental samples, degraded samples and samples in paraffin.<\/li>\n<li class=\"bullet-checkmark\"><strong>Intra- and interassay reproducibility<\/strong>: elimination of the bias derived from the amplification through PCR that allows for the quantification of small-scale differences.<\/li>\n<li class=\"bullet-checkmark\"><strong>Optimisation of laboratory resources<\/strong>: given the reaction volumes in the picolitre-nanolitre range, the use of reactants and the sample required is less for each experiment.<\/li>\n<\/ul>\n\t\t<\/div>\n\t\t\t\t\t<\/div>\n\n\t\n<\/div>\n\t<section class=\"section\" id=\"section_364687559\">\n\t\t<div class=\"bg section-bg fill bg-fill  bg-loaded\" >\n\n\t\t\t\n\t\t\t\n\t\t\t\n\n\t\t<\/div>\n\n\t\t\n\n\t\t<div class=\"section-content relative\">\n\t\t\t\n\n<div class=\"row row-small row-full-width align-center row-divided\"  id=\"row-37328872\">\n\n\n\t<div id=\"col-1789760780\" class=\"col medium-3 small-12 large-3\"  >\n\t\t\t\t<div class=\"col-inner text-left\"  >\n\t\t\t\n\t\t\t\n\n<div class=\"row\"  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