{"id":176,"date":"2016-05-30T11:44:04","date_gmt":"2016-05-30T09:44:04","guid":{"rendered":"https:\/\/www.genoscreen.fr\/sanger\/"},"modified":"2026-06-07T13:57:15","modified_gmt":"2026-06-07T11:57:15","slug":"sanger-sequencing","status":"publish","type":"page","link":"https:\/\/www.genoscreen.fr\/en\/genomic-services\/sequencing\/sanger-sequencing\/sanger-sequencing\/","title":{"rendered":"Sanger sequencing &#8211; The low-throughput genomics solution"},"content":{"rendered":"\n<p class=\"intro wp-block-paragraph\"><strong>Sanger sequencing<\/strong> is a well-proven, low-throughput analytical solution that is well suited to fragments of all sizes (<strong>100-1200 bp read length<\/strong>). GenoScreen\u2019s Sanger sequencing services can be adapted to suit all types of project, regardless the size, delay time or frequency. <\/p>\n\n<div class=\"wp-block-buttons is-content-justification-center is-layout-flex wp-container-core-buttons-is-layout-04478499 wp-block-buttons-is-layout-flex\" style=\"margin-top:20px;margin-bottom:20px\">\n<div class=\"wp-block-button\"><a class=\"wp-block-button__link has-elementor-28-fc-130-color has-elementor-primary-background-color has-text-color has-background has-link-color wp-element-button\" href=\"mailto:contact@genoscreen.fr?subject=(Sanger)\" style=\"border-top-left-radius:0px;border-top-right-radius:0px;border-bottom-left-radius:0px;border-bottom-right-radius:0px\">Contact us!<\/a><\/div>\n<\/div>\n\n<h2 class=\"wp-block-heading has-text-align-center\">Sanger sequencing applications<\/h2>\n\n<p class=\"wp-block-paragraph\">Despite the emergence of new generation technologies (NGS), <strong>Sanger sequencing remains a reference method<\/strong> in many fields thanks to its <strong>reliability and accuracy<\/strong>.<\/p>\n\n\n<p class=\"has-text-align-center wp-block-paragraph\">Flexible and available, our teams carry out sequencing <strong>from sample preparation to data analysis<\/strong>. See <strong>our documentation below<\/strong> to find out more about our services and to prepare your sequencing request form. <\/p>\n\n<div class=\"wf-columns wf-columns-stack-medium wf-column\" data-wf-columns=\"1\">\n<figure><\/figure><\/div>\n\n<div class=\"wp-block-columns is-layout-flex wp-container-core-columns-is-layout-7387b849 wp-block-columns-is-layout-flex\">\n<div class=\"wp-block-column is-layout-flow wp-block-column-is-layout-flow\">\n<h3 class=\"wp-block-heading has-text-align-center\">User manual<\/h3>\n\n\n\n<figure class=\"wp-block-image size-full\"><a href=\"\/catalogues\/Sanger_User_Manual_2025.pdf\"><img decoding=\"async\" width=\"320\" height=\"100\" src=\"https:\/\/www.genoscreen.fr\/wp-content\/uploads\/telechargez_notre_guide_dusage.png\" alt=\"Download our user manual\" class=\"wp-image-1019\"\/><\/a><\/figure>\n<\/div>\n\n\n\n<div class=\"wp-block-column is-layout-flow wp-block-column-is-layout-flow\">\n<h3 class=\"wp-block-heading has-text-align-center\">Form (without purification)<\/h3>\n\n\n\n<figure class=\"wp-block-image\"><a href=\"\/document\/GENOSCREEN_Sanger_formulaire_avec_purif-2024.xlsx\"><img decoding=\"async\" width=\"320\" height=\"100\" src=\"https:\/\/www.genoscreen.fr\/wp-content\/uploads\/sequencage_avec_purification.png\" alt=\"Sequencing with purification\" class=\"wp-image-1021\"\/><\/a><\/figure>\n<\/div>\n\n\n\n<div class=\"wp-block-column is-layout-flow wp-block-column-is-layout-flow\">\n<h3 class=\"wp-block-heading has-text-align-center\">Form (with purification)<\/h3>\n\n\n\n<figure class=\"wp-block-image\"><a href=\"\/document\/GENOSCREEN_Sanger_formulaire_sans_purif-2024.xlsx\"><img decoding=\"async\" width=\"320\" height=\"100\" src=\"https:\/\/www.genoscreen.fr\/wp-content\/uploads\/sequencage_sans_purification.png\" alt=\"Sequencing without purification\" class=\"wp-image-1023\"\/><\/a><\/figure>\n<\/div>\n<\/div>\n\n<h3 class=\"wp-block-heading has-text-align-center\">Premium range<\/h3>\n\n<div class=\"wp-block-columns is-layout-flex wp-container-core-columns-is-layout-7387b849 wp-block-columns-is-layout-flex\">\n<div class=\"wp-block-column is-layout-flow wp-block-column-is-layout-flow\">\n<p class=\"wp-block-paragraph\">The Premium offers correspond to a complete and personalised analysis of samples:<\/p>\n\n\n\n<ul class=\"wp-block-list\">\n<li><strong>Adaptation of the protocol<\/strong> to GC-rich sequences<\/li>\n\n\n\n<li><strong>Supply of universal primers<\/strong><\/li>\n\n\n\n<li>Sequence reading <strong>up to 1200 bp<\/strong><\/li>\n\n\n\n<li>Results sent within <strong>24 to 48 hours<\/strong><\/li>\n<\/ul>\n<\/div>\n\n\n\n<div class=\"wp-block-column is-layout-flow wp-block-column-is-layout-flow\">\n<figure class=\"wp-block-image aligncenter is-resized\"><img loading=\"lazy\" decoding=\"async\" width=\"500\" height=\"500\" src=\"https:\/\/www.genoscreen.fr\/wp-content\/uploads\/resultats_Sanger_sous_24_a_48h.png\" alt=\"Sanger results within 24 to 48 hours\" class=\"wp-image-1024\" style=\"width:200px\" title=\"Sanger results within 24 to 48 hours\" srcset=\"https:\/\/www.genoscreen.fr\/wp-content\/uploads\/resultats_Sanger_sous_24_a_48h.png 500w, https:\/\/www.genoscreen.fr\/wp-content\/uploads\/resultats_Sanger_sous_24_a_48h-300x300.png 300w\" sizes=\"(max-width: 500px) 100vw, 500px\" \/><\/figure>\n<\/div>\n<\/div>\n\n<p class=\"wp-block-paragraph\">The Premium range gives you access to our hotline, by phone and email: <strong>expert scientific support<\/strong> for sequence profile analysis.<\/p>\n\n<h4 class=\"wp-block-heading has-text-align-center\">Workflow tailored to your needs<\/h4>\n\n\n\n<p class=\"wp-block-paragraph\">All our offers are open to different sample formats:<\/p>\n\n<ul class=\"wp-block-list\">\n<li><strong>tubes<\/strong><\/li>\n\n\n\n<li><strong>strips<\/strong><\/li>\n\n\n\n<li><strong>plates<\/strong>, complete or not<\/li>\n<\/ul>\n\n<p class=\"wp-block-paragraph\">Our One-Shot Plus and Optimized offers include additional information:<\/p>\n\n<ul class=\"wp-block-list\">\n<li><strong>Signal optimisation<\/strong><\/li>\n\n\n\n<li><strong>Reduction of any backgroun noise<\/strong><\/li>\n\n\n\n<li>Assignment of indeterminate bases<\/li>\n\n\n\n<li><strong>A specific protocol for mutation detection<\/strong><\/li>\n<\/ul>\n\n<h4 class=\"wp-block-heading has-text-align-center\">Additional analyses<\/h4>\n\n<p class=\"wp-block-paragraph\">GenoScreen offers a range of <strong>services to complement sequencing:<\/strong><\/p>\n\n\n<div class=\"wp-block-buttons is-content-justification-center is-layout-flex wp-container-core-buttons-is-layout-04478499 wp-block-buttons-is-layout-flex\" style=\"margin-top:20px;margin-bottom:20px\">\n<div class=\"wp-block-button\"><a class=\"wp-block-button__link has-elementor-28-fc-130-color has-elementor-primary-background-color has-text-color has-background has-link-color wp-element-button\" href=\"https:\/\/www.genoscreen.fr\/en\/genomic-services\/request-a-quote-genomic-analysis\" style=\"border-top-left-radius:0px;border-top-right-radius:0px;border-bottom-left-radius:0px;border-bottom-right-radius:0px\">Request a quote<\/a><\/div>\n<\/div>\n\n<h3 class=\"wp-block-heading has-text-align-center\">Economic range<\/h3>\n\n<p class=\"wp-block-paragraph\">All the quality and responsiveness of GenoScreen at a low price!<\/p>\n\n<p class=\"wp-block-paragraph\">Using your <strong>own PCR product + primer mix<\/strong> or even the sequencing reaction you have produced, we can take your samples to a more advanced stage for an optimised price.<\/p>\n\n\n<div class=\"wp-block-columns is-layout-flex wp-container-core-columns-is-layout-7387b849 wp-block-columns-is-layout-flex\">\n<div class=\"wp-block-column is-layout-flow wp-block-column-is-layout-flow\">\n<h2 class=\"wp-block-heading\">The GenoScreen&#8217;s assets<\/h2>\n\n\n\n<ul class=\"wp-block-list\">\n<li><p>Flexible <strong>sequencing <\/strong>offer that adapts to your needs<\/p><\/li>\n\n\n\n<li><p><strong>Personalised monitoring<\/strong> of your projects<\/p><\/li>\n\n\n\n<li><p>Simple ordering system<\/p><\/li>\n\n\n\n<li><p>Monthly invoicing or <strong>prepaid account<\/strong><\/p><\/li>\n\n\n\n<li><p><strong>Free transport<\/strong> of your samples by a GenoScreen-approved operator<\/p><\/li>\n\n\n\n<li><p>Optimised protection of samples in <strong>Genobox<\/strong><\/p><br\/><\/li>\n<\/ul>\n<\/div>\n\n\n\n<div class=\"wp-block-column is-layout-flow wp-block-column-is-layout-flow\">\n<figure class=\"wp-block-image aligncenter is-resized\"><img loading=\"lazy\" decoding=\"async\" width=\"1097\" height=\"981\" src=\"https:\/\/www.genoscreen.fr\/wp-content\/uploads\/GenoBox_GenoScreen.png\" alt=\"GenoBox_GenoScreen.png\" class=\"wp-image-1025\" style=\"width:320px\" srcset=\"https:\/\/www.genoscreen.fr\/wp-content\/uploads\/GenoBox_GenoScreen.png 1097w, https:\/\/www.genoscreen.fr\/wp-content\/uploads\/GenoBox_GenoScreen-600x537.png 600w, https:\/\/www.genoscreen.fr\/wp-content\/uploads\/GenoBox_GenoScreen-768x687.png 768w\" sizes=\"(max-width: 1097px) 100vw, 1097px\" \/><\/figure>\n<\/div>\n<\/div>\n\n<div class=\"wf-column\"><\/div>\n","protected":false},"excerpt":{"rendered":"<p class=\"intro\"><strong>Sanger sequencing<\/strong>&nbsp;is a well-proven,&nbsp;<strong>low-throughput<\/strong>&nbsp;analytical solution that is well suited to fragments of all sizes (100-1200 bp read length). GenoScreen\u2019s&nbsp;<strong>Sanger sequencing services<\/strong>&nbsp;can be adapted to suit all types of project, regardless the size, delay time or frequency.<\/p>\n<p>&nbsp;<\/p>\n<p style=\"text-align: center;\"><a href=\"mailto:contact@genoscreen.fr?subject=(Sanger)\" class=\"lbtnContact\">Contact us!<\/a><\/p>\n<p>&nbsp;<\/p>\n<h2 style=\"text-align: center;\">Sanger sequencing applications<\/h2>\n<p>&nbsp;<\/p>\n<p>Despite the emergence of new generation technologies (NGS), Sanger sequencing remains a <strong>reference method<\/strong> in many fields thanks to its reliability and accuracy.<\/p>\n<p>&nbsp;<\/p>\n<div>smartslider3[556]<\/div>\n<p>&nbsp;<\/p>\n<p style=\"text-align: center;\">Flexible and available, our teams carry out sequencing from<strong> sample preparation to data analysis<\/strong>. <strong>See our documentation below<\/strong> to find out more about our services and to prepare your sequencing request form.<\/p>\n<p style=\"text-align: center;\">&nbsp;<\/p>\n<div class=\"wf-columns wf-columns-stack-medium\" data-wf-columns=\"1\">\n<div class=\"wf-column\">\n<h3 style=\"text-align: center;\">User manual<\/h3>\n<div class=\"wf-columns wf-columns-stack-medium\" data-wf-columns=\"1\">\n<div class=\"wf-columns wf-columns-stack-medium wf-column\" data-wf-columns=\"1\">\n<div class=\"wf-column\" style=\"text-align: center;\"><a href=\"https:\/\/www.genoscreen.fr\/wp-content\/uploads\/catalogues\/Sanger_User_Manual_2025.pdf\"><img loading=\"lazy\" decoding=\"async\" class=\" size-full wp-image-1077\" src=\"https:\/\/www.genoscreen.fr\/wp-content\/uploads\/download_our-user-manual.png\" alt=\"download our user manual\" width=\"198\" height=\"62\" onmouseover=\"this.src='images\/download_our-user-manual_click.png';\" onmouseout=\"this.src='https:\/\/www.genoscreen.fr\/wp-content\/uploads\/download_our-user-manual.png';\" \/><\/a>&nbsp;<\/div>\n<\/div>\n<\/div>\n<\/div>\n<div class=\"wf-column\">\n<h3 style=\"text-align: center;\">Form (with purification)<\/h3>\n<div class=\"wf-columns wf-columns-stack-medium\" data-wf-columns=\"1\">\n<div class=\"wf-columns wf-columns-stack-medium wf-column\" data-wf-columns=\"1\">\n<div class=\"wf-column\" style=\"text-align: center;\"><a href=\"https:\/\/www.genoscreen.fr\/wp-content\/uploads\/document\/GENOSCREEN_Sanger_formulaire_avec_purif-2024.xlsx\"><img loading=\"lazy\" decoding=\"async\" class=\" size-full wp-image-1078\" src=\"https:\/\/www.genoscreen.fr\/wp-content\/uploads\/sequencing_with-purification.png\" alt=\"s\u00e9quen\u00e7age avec purification\" width=\"198\" height=\"62\" style=\"display: block; margin-left: auto; margin-right: auto;\" onmouseover=\"this.src='images\/sequencing_with-purification_click.png';\" onmouseout=\"this.src='https:\/\/www.genoscreen.fr\/wp-content\/uploads\/sequencing_with-purification.png';\" \/><\/a><\/div>\n<\/div>\n<\/div>\n<\/div>\n<div class=\"wf-column\">\n<h3 style=\"text-align: center;\">Form (without purification)<\/h3>\n<div class=\"wf-columns wf-columns-stack-medium\" data-wf-columns=\"1\">\n<div class=\"wf-columns wf-columns-stack-medium wf-column\" data-wf-columns=\"1\">\n<div class=\"wf-column\" style=\"text-align: center;\"><a href=\"https:\/\/www.genoscreen.fr\/wp-content\/uploads\/document\/GENOSCREEN_Sanger_formulaire_sans_purif-2024.xlsx\"><img loading=\"lazy\" decoding=\"async\" class=\" size-full wp-image-1079\" src=\"https:\/\/www.genoscreen.fr\/wp-content\/uploads\/sequencing_without-purification.png\" alt=\"s\u00e9quen\u00e7age sans purification\" width=\"198\" height=\"62\" onmouseover=\"this.src='images\/sequencing_without-purification_click.png';\" onmouseout=\"this.src='https:\/\/www.genoscreen.fr\/wp-content\/uploads\/sequencing_without-purification.png';\" \/><\/a>&nbsp;<\/div>\n<\/div>\n<\/div>\n<\/div>\n<\/div>\n<p>&nbsp;<\/p>\n<p>&nbsp;&nbsp;<\/p>\n<h3 style=\"text-align: center;\">Premium range<\/h3>\n<p>The Premium offers correspond to a <strong>complete and personalised analysis of samples<\/strong>:<img loading=\"lazy\" decoding=\"async\" class=\" alignright size-full wp-image-1080\" src=\"https:\/\/www.genoscreen.fr\/wp-content\/uploads\/from_3_to_5_working_days.png\" alt=\"r\u00e9sultats Sanger sous 24 \u00e0 48h\" width=\"150\" height=\"150\" style=\"float: right;\" title=\"r\u00e9sultats Sanger sous 24 \u00e0 48h\" srcset=\"https:\/\/www.genoscreen.fr\/wp-content\/uploads\/from_3_to_5_working_days.png 500w, https:\/\/www.genoscreen.fr\/wp-content\/uploads\/from_3_to_5_working_days-300x300.png 300w\" sizes=\"(max-width: 150px) 100vw, 150px\" \/><\/p>\n<ul>\n<li><strong>Adaptation of the protocol<\/strong> to GC-rich sequences<\/li>\n<li><strong>Supply of universal primers<\/strong><\/li>\n<li>Sequence reading <strong>up to 1200 bp<\/strong><\/li>\n<li>Results sent <strong>within 24 to 48 hours<\/strong><\/li>\n<\/ul>\n<p>&nbsp;<\/p>\n<p>The Premium range gives you access to our hotline, by phone and email: expert <strong>scientific support<\/strong> for sequence profile analysis.<\/p>\n<p>&nbsp;<\/p>\n<h4 style=\"text-align: center;\">Workflow tailored to your needs<\/h4>\n<p>smartslider3[563]<\/p>\n<div>smartslider3[564]<\/div>\n<p>&nbsp;<\/p>\n<p>All our offers are open to different sample formats:<\/p>\n<ul>\n<li><strong>tubes<\/strong><\/li>\n<li><strong>strips<\/strong><\/li>\n<li><strong>plates<\/strong>, complete or not<\/li>\n<\/ul>\n<p>&nbsp;<\/p>\n<p>Our One-Shot Plus and Optimized offers include additional information:<\/p>\n<ul>\n<li>Signal optimisation<\/li>\n<li>Reduction of any backgroun noise<\/li>\n<li>Assignment of indeterminate bases<\/li>\n<li>A specific protocol for mutation detection<\/li>\n<\/ul>\n<p>&nbsp;<\/p>\n<h4 style=\"text-align: center;\">Additional analyses<\/h4>\n<p style=\"text-align: justify;\">&nbsp;<\/p>\n<p>Genoscreen offers a range of <strong>services to complement sequencing<\/strong>:<\/p>\n<div>smartslider3[255]<\/div>\n<p>&nbsp;<\/p>\n<p style=\"text-align: center;\"><a href=\"en\/genomic-services\/request-a-quote-genomic-analysis\" class=\"lbtnContact\">Ask for a quote<\/a><\/p>\n<div id=\"g\u00e9notypageseq\">&nbsp;<\/div>\n<p>&nbsp;<\/p>\n<h3 style=\"text-align: center;\">Economic range<\/h3>\n<p style=\"text-align: justify;\">All the quality and responsiveness of Genoscreen at a low price!<\/p>\n<p>Using your own <strong>PCR product + primer mix<\/strong> or even the sequencing reaction you have produced, we can take your samples to a more advanced stage for an optimised price.<\/p>\n<p>&nbsp;<\/p>\n<p>&nbsp;<\/p>\n<div>smartslider3[565]<\/div>\n<p>&nbsp;<\/p>\n<div class=\"wf-columns wf-columns-stack-medium\" data-wf-columns=\"1\">\n<div class=\"wf-column\">\n<h2>GenoScreen advantages<\/h2>\n<ul>\n<li>Flexible <strong>sequencing<\/strong> offer that adapts to your needs<\/li>\n<li>\n<p><strong>Personalised monitoring<\/strong> of your projects<\/p>\n<\/li>\n<li>\n<p>Simple ordering system<\/p>\n<\/li>\n<li>\n<p>Monthly invoicing or <strong>prepaid account<\/strong><\/p>\n<\/li>\n<li>\n<p><strong>Free transport of your samples<\/strong> by a GenoScreen-approved operator<\/p>\n<\/li>\n<li>\n<p>Optimised protection of samples in <strong>Genobox<\/strong><\/p>\n<\/li>\n<\/ul>\n<\/div>\n<div class=\"wf-column\"><img loading=\"lazy\" decoding=\"async\" class=\" alignright size-full wp-image-1025\" src=\"https:\/\/www.genoscreen.fr\/wp-content\/uploads\/GenoBox_GenoScreen.png\" alt=\"GenoBox_GenoScreen.png\" width=\"323\" height=\"323\" style=\"float: right;\" \/><\/div>\n<\/div>\n","protected":false},"author":1,"featured_media":1017,"parent":2274,"menu_order":12,"comment_status":"closed","ping_status":"closed","template":"","meta":{"footnotes":""},"page-categories":[158],"class_list":["post-176","page","type-page","status-publish","has-post-thumbnail","hentry","page-categories-genoscreen-services"],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v28.3 - https:\/\/yoast.com\/product\/yoast-seo-wordpress\/ -->\n<title>Sanger sequencing - The low-throughput genomics solution - GenoScreen<\/title>\n<meta name=\"description\" content=\"Sanger Genoscreen sequencing services are suitable for all types of genomic analysis projects.\" \/>\n<meta name=\"robots\" content=\"index, follow, max-snippet:-1, max-image-preview:large, max-video-preview:-1\" \/>\n<link rel=\"canonical\" href=\"https:\/\/www.genoscreen.fr\/en\/genomic-services\/sequencing\/sanger-sequencing\/sanger-sequencing\/\" \/>\n<meta property=\"og:locale\" content=\"en_US\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"Sanger sequencing - The low-throughput genomics solution - GenoScreen\" \/>\n<meta property=\"og:description\" content=\"Sanger Genoscreen sequencing services are suitable for all types of genomic analysis projects.\" \/>\n<meta property=\"og:url\" content=\"https:\/\/www.genoscreen.fr\/en\/genomic-services\/sequencing\/sanger-sequencing\/sanger-sequencing\/\" \/>\n<meta property=\"og:site_name\" content=\"GenoScreen\" \/>\n<meta property=\"article:modified_time\" content=\"2026-06-07T11:57:15+00:00\" \/>\n<meta property=\"og:image\" content=\"https:\/\/www.genoscreen.fr\/wp-content\/uploads\/genoscreen-services\/sanger.jpg\" \/>\n\t<meta property=\"og:image:width\" content=\"1204\" \/>\n\t<meta property=\"og:image:height\" content=\"627\" \/>\n\t<meta property=\"og:image:type\" content=\"image\/jpeg\" \/>\n<meta name=\"twitter:card\" content=\"summary_large_image\" \/>\n<meta name=\"twitter:site\" content=\"@genoscreen\" \/>\n<meta name=\"twitter:label1\" content=\"Est. reading time\" \/>\n\t<meta name=\"twitter:data1\" content=\"2 minutes\" \/>\n<script type=\"application\/ld+json\" class=\"yoast-schema-graph\">{\"@context\":\"https:\\\/\\\/schema.org\",\"@graph\":[{\"@type\":\"WebPage\",\"@id\":\"https:\\\/\\\/www.genoscreen.fr\\\/en\\\/genomic-services\\\/sequencing\\\/sanger-sequencing\\\/sanger-sequencing\\\/\",\"url\":\"https:\\\/\\\/www.genoscreen.fr\\\/en\\\/genomic-services\\\/sequencing\\\/sanger-sequencing\\\/sanger-sequencing\\\/\",\"name\":\"Sanger sequencing - The low-throughput genomics solution - GenoScreen\",\"isPartOf\":{\"@id\":\"https:\\\/\\\/www.genoscreen.fr\\\/en\\\/#website\"},\"primaryImageOfPage\":{\"@id\":\"https:\\\/\\\/www.genoscreen.fr\\\/en\\\/genomic-services\\\/sequencing\\\/sanger-sequencing\\\/sanger-sequencing\\\/#primaryimage\"},\"image\":{\"@id\":\"https:\\\/\\\/www.genoscreen.fr\\\/en\\\/genomic-services\\\/sequencing\\\/sanger-sequencing\\\/sanger-sequencing\\\/#primaryimage\"},\"thumbnailUrl\":\"https:\\\/\\\/www.genoscreen.fr\\\/wp-content\\\/uploads\\\/genoscreen-services\\\/sanger.jpg\",\"datePublished\":\"2016-05-30T09:44:04+00:00\",\"dateModified\":\"2026-06-07T11:57:15+00:00\",\"description\":\"Sanger Genoscreen sequencing services are suitable for all types of genomic analysis projects.\",\"breadcrumb\":{\"@id\":\"https:\\\/\\\/www.genoscreen.fr\\\/en\\\/genomic-services\\\/sequencing\\\/sanger-sequencing\\\/sanger-sequencing\\\/#breadcrumb\"},\"inLanguage\":\"en-US\",\"potentialAction\":[{\"@type\":\"ReadAction\",\"target\":[\"https:\\\/\\\/www.genoscreen.fr\\\/en\\\/genomic-services\\\/sequencing\\\/sanger-sequencing\\\/sanger-sequencing\\\/\"]}]},{\"@type\":\"ImageObject\",\"inLanguage\":\"en-US\",\"@id\":\"https:\\\/\\\/www.genoscreen.fr\\\/en\\\/genomic-services\\\/sequencing\\\/sanger-sequencing\\\/sanger-sequencing\\\/#primaryimage\",\"url\":\"https:\\\/\\\/www.genoscreen.fr\\\/wp-content\\\/uploads\\\/genoscreen-services\\\/sanger.jpg\",\"contentUrl\":\"https:\\\/\\\/www.genoscreen.fr\\\/wp-content\\\/uploads\\\/genoscreen-services\\\/sanger.jpg\",\"width\":1204,\"height\":627,\"caption\":\"S\u00e9quen\u00e7age Sanger - La solution g\u00e9nomique bas d\u00e9bit\"},{\"@type\":\"BreadcrumbList\",\"@id\":\"https:\\\/\\\/www.genoscreen.fr\\\/en\\\/genomic-services\\\/sequencing\\\/sanger-sequencing\\\/sanger-sequencing\\\/#breadcrumb\",\"itemListElement\":[{\"@type\":\"ListItem\",\"position\":1,\"name\":\"Home\",\"item\":\"https:\\\/\\\/www.genoscreen.fr\\\/en\\\/\"},{\"@type\":\"ListItem\",\"position\":2,\"name\":\"Genomic Services\",\"item\":\"https:\\\/\\\/www.genoscreen.fr\\\/en\\\/services-genomiques\\\/\"},{\"@type\":\"ListItem\",\"position\":3,\"name\":\"Sequencing\",\"item\":\"https:\\\/\\\/www.genoscreen.fr\\\/en\\\/services-genomiques\\\/sequencage-sanger-ngs\\\/\"},{\"@type\":\"ListItem\",\"position\":4,\"name\":\"Sanger Sequencing\",\"item\":\"https:\\\/\\\/www.genoscreen.fr\\\/en\\\/genomic-services\\\/sequencing\\\/sanger-sequencing\\\/\"},{\"@type\":\"ListItem\",\"position\":5,\"name\":\"Sanger sequencing &#8211; The low-throughput genomics solution\"}]},{\"@type\":\"WebSite\",\"@id\":\"https:\\\/\\\/www.genoscreen.fr\\\/en\\\/#website\",\"url\":\"https:\\\/\\\/www.genoscreen.fr\\\/en\\\/\",\"name\":\"GenoScreen\",\"description\":\"Sp\u00e9cialiste de la g\u00e9nomique et de la bioinformatique depuis 2001\",\"publisher\":{\"@id\":\"https:\\\/\\\/www.genoscreen.fr\\\/en\\\/#organization\"},\"potentialAction\":[{\"@type\":\"SearchAction\",\"target\":{\"@type\":\"EntryPoint\",\"urlTemplate\":\"https:\\\/\\\/www.genoscreen.fr\\\/en\\\/?s={search_term_string}\"},\"query-input\":{\"@type\":\"PropertyValueSpecification\",\"valueRequired\":true,\"valueName\":\"search_term_string\"}}],\"inLanguage\":\"en-US\"},{\"@type\":\"Organization\",\"@id\":\"https:\\\/\\\/www.genoscreen.fr\\\/en\\\/#organization\",\"name\":\"GenoScreen\",\"url\":\"https:\\\/\\\/www.genoscreen.fr\\\/en\\\/\",\"logo\":{\"@type\":\"ImageObject\",\"inLanguage\":\"en-US\",\"@id\":\"https:\\\/\\\/www.genoscreen.fr\\\/en\\\/#\\\/schema\\\/logo\\\/image\\\/\",\"url\":\"https:\\\/\\\/www.genoscreen.fr\\\/wp-content\\\/uploads\\\/logo-genoscreen-1.svg\",\"contentUrl\":\"https:\\\/\\\/www.genoscreen.fr\\\/wp-content\\\/uploads\\\/logo-genoscreen-1.svg\",\"width\":267,\"height\":91,\"caption\":\"GenoScreen\"},\"image\":{\"@id\":\"https:\\\/\\\/www.genoscreen.fr\\\/en\\\/#\\\/schema\\\/logo\\\/image\\\/\"},\"sameAs\":[\"https:\\\/\\\/x.com\\\/genoscreen\",\"https:\\\/\\\/fr.linkedin.com\\\/company\\\/genoscreen\"]}]}<\/script>\n<!-- \/ Yoast SEO plugin. -->","yoast_head_json":{"title":"Sanger sequencing - The low-throughput genomics solution - GenoScreen","description":"Sanger Genoscreen sequencing services are suitable for all types of genomic analysis projects.","robots":{"index":"index","follow":"follow","max-snippet":"max-snippet:-1","max-image-preview":"max-image-preview:large","max-video-preview":"max-video-preview:-1"},"canonical":"https:\/\/www.genoscreen.fr\/en\/genomic-services\/sequencing\/sanger-sequencing\/sanger-sequencing\/","og_locale":"en_US","og_type":"article","og_title":"Sanger sequencing - The low-throughput genomics solution - GenoScreen","og_description":"Sanger Genoscreen sequencing services are suitable for all types of genomic analysis projects.","og_url":"https:\/\/www.genoscreen.fr\/en\/genomic-services\/sequencing\/sanger-sequencing\/sanger-sequencing\/","og_site_name":"GenoScreen","article_modified_time":"2026-06-07T11:57:15+00:00","og_image":[{"width":1204,"height":627,"url":"https:\/\/www.genoscreen.fr\/wp-content\/uploads\/genoscreen-services\/sanger.jpg","type":"image\/jpeg"}],"twitter_card":"summary_large_image","twitter_site":"@genoscreen","twitter_misc":{"Est. reading time":"2 minutes"},"schema":{"@context":"https:\/\/schema.org","@graph":[{"@type":"WebPage","@id":"https:\/\/www.genoscreen.fr\/en\/genomic-services\/sequencing\/sanger-sequencing\/sanger-sequencing\/","url":"https:\/\/www.genoscreen.fr\/en\/genomic-services\/sequencing\/sanger-sequencing\/sanger-sequencing\/","name":"Sanger sequencing - The low-throughput genomics solution - GenoScreen","isPartOf":{"@id":"https:\/\/www.genoscreen.fr\/en\/#website"},"primaryImageOfPage":{"@id":"https:\/\/www.genoscreen.fr\/en\/genomic-services\/sequencing\/sanger-sequencing\/sanger-sequencing\/#primaryimage"},"image":{"@id":"https:\/\/www.genoscreen.fr\/en\/genomic-services\/sequencing\/sanger-sequencing\/sanger-sequencing\/#primaryimage"},"thumbnailUrl":"https:\/\/www.genoscreen.fr\/wp-content\/uploads\/genoscreen-services\/sanger.jpg","datePublished":"2016-05-30T09:44:04+00:00","dateModified":"2026-06-07T11:57:15+00:00","description":"Sanger Genoscreen sequencing services are suitable for all types of genomic analysis projects.","breadcrumb":{"@id":"https:\/\/www.genoscreen.fr\/en\/genomic-services\/sequencing\/sanger-sequencing\/sanger-sequencing\/#breadcrumb"},"inLanguage":"en-US","potentialAction":[{"@type":"ReadAction","target":["https:\/\/www.genoscreen.fr\/en\/genomic-services\/sequencing\/sanger-sequencing\/sanger-sequencing\/"]}]},{"@type":"ImageObject","inLanguage":"en-US","@id":"https:\/\/www.genoscreen.fr\/en\/genomic-services\/sequencing\/sanger-sequencing\/sanger-sequencing\/#primaryimage","url":"https:\/\/www.genoscreen.fr\/wp-content\/uploads\/genoscreen-services\/sanger.jpg","contentUrl":"https:\/\/www.genoscreen.fr\/wp-content\/uploads\/genoscreen-services\/sanger.jpg","width":1204,"height":627,"caption":"S\u00e9quen\u00e7age Sanger - La solution g\u00e9nomique bas d\u00e9bit"},{"@type":"BreadcrumbList","@id":"https:\/\/www.genoscreen.fr\/en\/genomic-services\/sequencing\/sanger-sequencing\/sanger-sequencing\/#breadcrumb","itemListElement":[{"@type":"ListItem","position":1,"name":"Home","item":"https:\/\/www.genoscreen.fr\/en\/"},{"@type":"ListItem","position":2,"name":"Genomic Services","item":"https:\/\/www.genoscreen.fr\/en\/services-genomiques\/"},{"@type":"ListItem","position":3,"name":"Sequencing","item":"https:\/\/www.genoscreen.fr\/en\/services-genomiques\/sequencage-sanger-ngs\/"},{"@type":"ListItem","position":4,"name":"Sanger Sequencing","item":"https:\/\/www.genoscreen.fr\/en\/genomic-services\/sequencing\/sanger-sequencing\/"},{"@type":"ListItem","position":5,"name":"Sanger sequencing &#8211; The low-throughput genomics solution"}]},{"@type":"WebSite","@id":"https:\/\/www.genoscreen.fr\/en\/#website","url":"https:\/\/www.genoscreen.fr\/en\/","name":"GenoScreen","description":"Sp\u00e9cialiste de la g\u00e9nomique et de la bioinformatique depuis 2001","publisher":{"@id":"https:\/\/www.genoscreen.fr\/en\/#organization"},"potentialAction":[{"@type":"SearchAction","target":{"@type":"EntryPoint","urlTemplate":"https:\/\/www.genoscreen.fr\/en\/?s={search_term_string}"},"query-input":{"@type":"PropertyValueSpecification","valueRequired":true,"valueName":"search_term_string"}}],"inLanguage":"en-US"},{"@type":"Organization","@id":"https:\/\/www.genoscreen.fr\/en\/#organization","name":"GenoScreen","url":"https:\/\/www.genoscreen.fr\/en\/","logo":{"@type":"ImageObject","inLanguage":"en-US","@id":"https:\/\/www.genoscreen.fr\/en\/#\/schema\/logo\/image\/","url":"https:\/\/www.genoscreen.fr\/wp-content\/uploads\/logo-genoscreen-1.svg","contentUrl":"https:\/\/www.genoscreen.fr\/wp-content\/uploads\/logo-genoscreen-1.svg","width":267,"height":91,"caption":"GenoScreen"},"image":{"@id":"https:\/\/www.genoscreen.fr\/en\/#\/schema\/logo\/image\/"},"sameAs":["https:\/\/x.com\/genoscreen","https:\/\/fr.linkedin.com\/company\/genoscreen"]}]}},"_links":{"self":[{"href":"https:\/\/www.genoscreen.fr\/en\/wp-json\/wp\/v2\/pages\/176","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/www.genoscreen.fr\/en\/wp-json\/wp\/v2\/pages"}],"about":[{"href":"https:\/\/www.genoscreen.fr\/en\/wp-json\/wp\/v2\/types\/page"}],"author":[{"embeddable":true,"href":"https:\/\/www.genoscreen.fr\/en\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"https:\/\/www.genoscreen.fr\/en\/wp-json\/wp\/v2\/comments?post=176"}],"version-history":[{"count":5,"href":"https:\/\/www.genoscreen.fr\/en\/wp-json\/wp\/v2\/pages\/176\/revisions"}],"predecessor-version":[{"id":3441,"href":"https:\/\/www.genoscreen.fr\/en\/wp-json\/wp\/v2\/pages\/176\/revisions\/3441"}],"up":[{"embeddable":true,"href":"https:\/\/www.genoscreen.fr\/en\/wp-json\/wp\/v2\/pages\/2274"}],"wp:featuredmedia":[{"embeddable":true,"href":"https:\/\/www.genoscreen.fr\/en\/wp-json\/wp\/v2\/media\/1017"}],"wp:attachment":[{"href":"https:\/\/www.genoscreen.fr\/en\/wp-json\/wp\/v2\/media?parent=176"}],"wp:term":[{"taxonomy":"page-categories","embeddable":true,"href":"https:\/\/www.genoscreen.fr\/en\/wp-json\/wp\/v2\/page-categories?post=176"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}