{"id":6625,"date":"2024-11-15T12:55:32","date_gmt":"2024-11-15T12:55:32","guid":{"rendered":"https:\/\/staging.prodottigianni.com\/ngs\/"},"modified":"2025-10-02T11:25:12","modified_gmt":"2025-10-02T11:25:12","slug":"ngs","status":"publish","type":"page","link":"https:\/\/www.prodottigianni.com\/en\/life-science-services\/ngs\/","title":{"rendered":"NGS"},"content":{"rendered":"\t\t<div data-elementor-type=\"wp-page\" data-elementor-id=\"6625\" class=\"elementor elementor-6625 elementor-930\" data-elementor-post-type=\"page\">\n\t\t\t\t<div class=\"elementor-element elementor-element-1372e61 e-con-full e-flex e-con e-parent\" data-id=\"1372e61\" data-element_type=\"container\" data-e-type=\"container\" data-settings=\"{&quot;background_background&quot;:&quot;classic&quot;}\">\n\t\t<div class=\"elementor-element elementor-element-78b6efc e-con-full e-flex e-con e-child\" data-id=\"78b6efc\" data-element_type=\"container\" data-e-type=\"container\">\n\t\t\t\t<div class=\"elementor-element elementor-element-cc7c634 elementor-widget elementor-widget-heading\" data-id=\"cc7c634\" data-element_type=\"widget\" data-e-type=\"widget\" data-widget_type=\"heading.default\">\n\t\t\t\t<div class=\"elementor-widget-container\">\n\t\t\t\t\t<h1 class=\"elementor-heading-title elementor-size-default\">NGS<\/h1>\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t<div class=\"elementor-element elementor-element-8fee447 elementor-widget elementor-widget-heading\" data-id=\"8fee447\" data-element_type=\"widget\" data-e-type=\"widget\" data-widget_type=\"heading.default\">\n\t\t\t\t<div class=\"elementor-widget-container\">\n\t\t\t\t\t<h2 class=\"elementor-heading-title elementor-size-default\">Prodotti Gianni provides the \u201cextensive experience of its partners for the\u201d reliable execution of service experiments and custom production requests.<\/h2>\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t<div class=\"elementor-element elementor-element-ccb00b8 e-flex e-con-boxed e-con e-parent\" data-id=\"ccb00b8\" data-element_type=\"container\" data-e-type=\"container\">\n\t\t\t\t\t<div class=\"e-con-inner\">\n\t\t\t\t<div class=\"elementor-element elementor-element-ac6e523 elementor-widget elementor-widget-heading\" data-id=\"ac6e523\" data-element_type=\"widget\" data-e-type=\"widget\" data-widget_type=\"heading.default\">\n\t\t\t\t<div class=\"elementor-widget-container\">\n\t\t\t\t\t<h2 class=\"elementor-heading-title elementor-size-default\">Super-Long Read Sequencing Kit<\/h2>\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t<div class=\"elementor-element elementor-element-7da5781 elementor-widget elementor-widget-text-editor\" data-id=\"7da5781\" data-element_type=\"widget\" data-e-type=\"widget\" data-widget_type=\"text-editor.default\">\n\t\t\t\t<div class=\"elementor-widget-container\">\n\t\t\t\t\t\t\t\t\t<p>TELL-Seq\u2122 Kit from Universal Sequencing Technology enables the construction of NGS libraries with 200Kb fragments that can be sequenced with Illumina instruments. This transposase-based technology has a highly simplified, scalable protocol that takes 3 hours, can be performed in a PCR tube, and requires minimal DNA (0.2 ng for bacteria and 3 ng for humans). It&#8217;s an excellent solution for Whole Genome sequencing, Whole Genome phasing, de-novo assembly, metagenomics, and structural variant analysis.  <\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t<div class=\"elementor-element elementor-element-dbb3a5f e-flex e-con-boxed e-con e-parent\" data-id=\"dbb3a5f\" data-element_type=\"container\" data-e-type=\"container\">\n\t\t\t\t\t<div class=\"e-con-inner\">\n\t\t\t\t<div class=\"elementor-element elementor-element-c3955ce elementor-widget elementor-widget-heading\" data-id=\"c3955ce\" data-element_type=\"widget\" data-e-type=\"widget\" data-widget_type=\"heading.default\">\n\t\t\t\t<div class=\"elementor-widget-container\">\n\t\t\t\t\t<h2 class=\"elementor-heading-title elementor-size-default\">Super-Long Read Sequencing Kit<\/h2>\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t<div class=\"elementor-element elementor-element-f2eac13 elementor-widget elementor-widget-heading\" data-id=\"f2eac13\" data-element_type=\"widget\" data-e-type=\"widget\" data-widget_type=\"heading.default\">\n\t\t\t\t<div class=\"elementor-widget-container\">\n\t\t\t\t\t<h3 class=\"elementor-heading-title elementor-size-default\">CORALL Total and mRNA-Seq Library Prep Kits<\/h3>\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t<div class=\"elementor-element elementor-element-abd2236 elementor-widget elementor-widget-text-editor\" data-id=\"abd2236\" data-element_type=\"widget\" data-e-type=\"widget\" data-widget_type=\"text-editor.default\">\n\t\t\t\t<div class=\"elementor-widget-container\">\n\t\t\t\t\t\t\t\t\t<p><span style=\"font-weight: 400;\">These kits allow the preparation of RNA-Seq libraries that include UMI and UDI for whole transcriptome analysis using Illumina NGS platforms. The established CORALL technology, free from mechanical or enzymatic fragmentation, is completed in 6 steps (4.5 hours). It can be applied to all sample types, including degraded and FFPE samples, and offers exceptional performance on low-input samples, down to 1 ng of initial quantity before mRNA selection or ribo-depletion.   <\/span><\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t<div class=\"elementor-element elementor-element-939ebc4 elementor-widget elementor-widget-heading\" data-id=\"939ebc4\" data-element_type=\"widget\" data-e-type=\"widget\" data-widget_type=\"heading.default\">\n\t\t\t\t<div class=\"elementor-widget-container\">\n\t\t\t\t\t<h3 class=\"elementor-heading-title elementor-size-default\">Small RNA-Seq Library Prep Kit for Illumina\n<\/h3>\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t<div class=\"elementor-element elementor-element-8c8e42f elementor-widget elementor-widget-text-editor\" data-id=\"8c8e42f\" data-element_type=\"widget\" data-e-type=\"widget\" data-widget_type=\"text-editor.default\">\n\t\t\t\t<div class=\"elementor-widget-container\">\n\t\t\t\t\t\t\t\t\t<p><span style=\"font-weight: 400;\">Library preparation can be done starting directly from total RNA or enriched small RNA. The protocol takes 5 hours and the resulting libraries do not require gel purification. It is highly sensitive and therefore suitable for samples with low RNA content, exosomes, and liquid biopsies. The required sample range is from 100ng to 1,000ng of total RNA or from 50pg-1,000ng of enriched small RNA, including plasma, serum, and urine.   <\/span> <span style=\"font-weight: 400;\">It can include the TraPR kit for purification of only physiologically active Small RNAs.<\/span><\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t<div class=\"elementor-element elementor-element-5773371 e-flex e-con-boxed e-con e-parent\" data-id=\"5773371\" data-element_type=\"container\" data-e-type=\"container\">\n\t\t\t\t\t<div class=\"e-con-inner\">\n\t\t\t\t<div class=\"elementor-element elementor-element-a05b06d elementor-widget elementor-widget-heading\" data-id=\"a05b06d\" data-element_type=\"widget\" data-e-type=\"widget\" data-widget_type=\"heading.default\">\n\t\t\t\t<div class=\"elementor-widget-container\">\n\t\t\t\t\t<h2 class=\"elementor-heading-title elementor-size-default\">Expression Profiling Library Prep Kits<\/h2>\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t<div class=\"elementor-element elementor-element-70658f0 elementor-widget elementor-widget-heading\" data-id=\"70658f0\" data-element_type=\"widget\" data-e-type=\"widget\" data-widget_type=\"heading.default\">\n\t\t\t\t<div class=\"elementor-widget-container\">\n\t\t\t\t\t<h3 class=\"elementor-heading-title elementor-size-default\">QuantSeq 3' mRNA-Seq Library Prep Kits<\/h3>\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t<div class=\"elementor-element elementor-element-ba3216d elementor-widget elementor-widget-text-editor\" data-id=\"ba3216d\" data-element_type=\"widget\" data-e-type=\"widget\" data-widget_type=\"text-editor.default\">\n\t\t\t\t<div class=\"elementor-widget-container\">\n\t\t\t\t\t\t\t\t\t<p><span style=\"font-weight: 400;\">QuantSeq is the &#8220;gold standard&#8221; solution for differential expression analysis that allows for cost containment in sequencing while maintaining result quality. This approach creates a single fragment at the 3&#8242; UTR of each messenger with a protocol that doesn&#8217;t require poly(A) enrichment or rRNA depletion. The procedure is completed in 4.5 hours and can be successfully applied to degraded samples (e.g., FFPE) and blood samples where, thanks to the Globin Block Module, fragments from globin mRNA are not generated. The protocol is scalable and automatable, and in the REV version, it allows for the study of alternative polyadenylation sites.   <\/span><\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t<div class=\"elementor-element elementor-element-1da7ca6 e-flex e-con-boxed e-con e-parent\" data-id=\"1da7ca6\" data-element_type=\"container\" data-e-type=\"container\">\n\t\t\t\t\t<div class=\"e-con-inner\">\n\t\t\t\t<div class=\"elementor-element elementor-element-4071d73 elementor-widget elementor-widget-heading\" data-id=\"4071d73\" data-element_type=\"widget\" data-e-type=\"widget\" data-widget_type=\"heading.default\">\n\t\t\t\t<div class=\"elementor-widget-container\">\n\t\t\t\t\t<h2 class=\"elementor-heading-title elementor-size-default\">Single-cell RNA-Seq Kit<\/h2>\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t<div class=\"elementor-element elementor-element-30eacea elementor-widget elementor-widget-heading\" data-id=\"30eacea\" data-element_type=\"widget\" data-e-type=\"widget\" data-widget_type=\"heading.default\">\n\t\t\t\t<div class=\"elementor-widget-container\">\n\t\t\t\t\t<h3 class=\"elementor-heading-title elementor-size-default\">LUTHOR High-Definition Single-Cell 3' mRNA-Seq<\/h3>\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t<div class=\"elementor-element elementor-element-e0fa938 elementor-widget elementor-widget-text-editor\" data-id=\"e0fa938\" data-element_type=\"widget\" data-e-type=\"widget\" data-widget_type=\"text-editor.default\">\n\t\t\t\t<div class=\"elementor-widget-container\">\n\t\t\t\t\t\t\t\t\t<p><span style=\"font-weight: 400;\">Traditional single-cell RNA-Seq methods are based on sequencing thousands of cells with low read depth. While this approach is sufficient to identify cell types based on the detection of highly expressed genes,  <\/span><span style=\"font-weight: 400;\">it provides an incomplete picture of expressed genes and doesn&#8217;t allow for fine characterization of cell subpopulations. LUTHOR HD,  <\/span><span style=\"font-weight: 400;\">thanks to direct RNA \u201camplification, e\u201d nables high-definition scRNA-Seq with unprecedented sensitivity and resolution, a<\/span><span style=\"font-weight: 400;\">llowing the capture and sequencing of even poorly expressed genes and revealing the complete and real transcriptome of each cell (typically 95% of expressed genes with a read depth of 1M).<\/span> <span style=\"font-weight: 400;\">It provides the best results even with very low sample amounts: 1-100 cells or 10 pg-1 ng of total RNA, with the possibility of going down to 0.15 pg. It doesn&#8217;t  <\/span><span style=\"font-weight: 400;\">require RNA extraction, mRNA enrichment, or RNA depletion. Additionally, the \u201celimination of gDNA reduces bias, simplifies the\u201d data analysis, and allows for cost savings. The protocol takes 6 hours and can be applied to   <\/span><span style=\"font-weight: 400;\">single eukaryotic cells, cell biopsies, or purified total RNA <\/span><\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t<div class=\"elementor-element elementor-element-82600d5 e-flex e-con-boxed e-con e-parent\" data-id=\"82600d5\" data-element_type=\"container\" data-e-type=\"container\">\n\t\t\t\t\t<div class=\"e-con-inner\">\n\t\t\t\t<div class=\"elementor-element elementor-element-b98553e elementor-widget elementor-widget-heading\" data-id=\"b98553e\" data-element_type=\"widget\" data-e-type=\"widget\" data-widget_type=\"heading.default\">\n\t\t\t\t<div class=\"elementor-widget-container\">\n\t\t\t\t\t<h2 class=\"elementor-heading-title elementor-size-default\">NGS DNA Library Preparation by tagmentation<\/h2>\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t<div class=\"elementor-element elementor-element-85dbb1a elementor-widget elementor-widget-text-editor\" data-id=\"85dbb1a\" data-element_type=\"widget\" data-e-type=\"widget\" data-widget_type=\"text-editor.default\">\n\t\t\t\t<div class=\"elementor-widget-container\">\n\t\t\t\t\t\t\t\t\t<p><span style=\"font-weight: 400;\">The tagmentation protocol, which simultaneously fragments and ligates adapters for NGS DNA library preparation, has been perfected by SeqWell in a way never achieved before. This was possible by optimizing each kit reagent, but especially by engineering the Tn5 Transposase into a patented form called TnX that guarantees absolute reliability and specificity of operation. The library preparation protocol is thus reduced to just 3 steps (reaction setup \u2013 libraries amplification \u2013 pooling and purification) for 100 minutes, allowing up to 96 samples to be prepared simultaneously and therefore enabling extremely high throughput.  <\/span><\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t<div class=\"elementor-element elementor-element-d14dc44 e-flex e-con-boxed e-con e-parent\" data-id=\"d14dc44\" data-element_type=\"container\" data-e-type=\"container\">\n\t\t\t\t\t<div class=\"e-con-inner\">\n\t\t\t\t<div class=\"elementor-element elementor-element-7391619 elementor-widget elementor-widget-heading\" data-id=\"7391619\" data-element_type=\"widget\" data-e-type=\"widget\" data-widget_type=\"heading.default\">\n\t\t\t\t<div class=\"elementor-widget-container\">\n\t\t\t\t\t<h2 class=\"elementor-heading-title elementor-size-default\">3D Genomics<\/h2>\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t<div class=\"elementor-element elementor-element-5de53ff elementor-widget elementor-widget-text-editor\" data-id=\"5de53ff\" data-element_type=\"widget\" data-e-type=\"widget\" data-widget_type=\"text-editor.default\">\n\t\t\t\t<div class=\"elementor-widget-container\">\n\t\t\t\t\t\t\t\t\t<p><span style=\"font-weight: 400;\">3D genomics provides unprecedented access to the sequence, structure, and regulatory landscape of any genome. The Hi-C (High Throughput Chromatin Conformation Capture) technique that  <\/span><span style=\"font-weight: 400;\">allows visualization of how temporal and spatial changes in chromatin alter gene regulation and cellular functions, <\/span><span style=\"font-weight: 400;\">combines the Proximity Ligation assay with the NGS approach.<\/span><\/p><p><span style=\"font-weight: 400;\">This technique has been optimized in Arima Hi-C kits to achieve a more flexible, robust, and faster protocol that can be done in a single tube using 2 or 4 patented restriction enzymes and producing a much higher percentage of <\/span><i><span style=\"font-weight: 400;\">long-range cis interactions<\/span><\/i><span style=\"font-weight: 400;\"> compared to the classic approach at a lower cost.<\/span> <span style=\"font-weight: 400;\">There are multiple applications for 3D genomics. In cancer research,  <\/span><i><span style=\"font-weight: 400;\">it enables the discovery <\/span><\/i><span style=\"font-weight: 400;\">of structural variants for a complete understanding of disease mechanisms, <\/span><i><span style=\"font-weight: 400;\">biomarker discovery, and new therapeutic approaches thanks to insights into the sequence, structure, and regulatory landscape of cancer genomes.<\/span><\/i><span style=\"font-weight: 400;\"> <\/span><\/p><p><span style=\"font-weight: 400;\">  Understanding how spatial relationships in genome structure influence gene regulation, cell development, and pathological processes supports epigenetic studies, while the \u201cassembly of chromosome-scale genomes helps explore the\u201d evolution of species.<\/span><\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t","protected":false},"excerpt":{"rendered":"<p>NGS Prodotti Gianni provides the \u201cextensive experience of its partners for the\u201d reliable execution of service experiments and custom production requests. Super-Long Read Sequencing Kit TELL-Seq\u2122 Kit from Universal Sequencing Technology enables the construction of NGS libraries with 200Kb fragments that can be sequenced with Illumina instruments. This transposase-based technology has a highly simplified, scalable [&hellip;]<\/p>\n","protected":false},"author":1,"featured_media":0,"parent":0,"menu_order":0,"comment_status":"closed","ping_status":"closed","template":"elementor_header_footer","meta":{"_mc_calendar":[],"footnotes":""},"class_list":["post-6625","page","type-page","status-publish","hentry"],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v27.3 - https:\/\/yoast.com\/product\/yoast-seo-wordpress\/ -->\r\n<title>NGS - Prodotti Gianni<\/title>\r\n<meta name=\"robots\" content=\"index, follow, max-snippet:-1, max-image-preview:large, max-video-preview:-1\" \/>\r\n<link rel=\"canonical\" href=\"https:\/\/www.prodottigianni.com\/en\/life-science-services\/ngs\/\" \/>\r\n<meta property=\"og:locale\" content=\"en_US\" \/>\r\n<meta property=\"og:type\" content=\"article\" \/>\r\n<meta property=\"og:title\" content=\"NGS - Prodotti Gianni\" \/>\r\n<meta property=\"og:description\" content=\"NGS Prodotti Gianni provides the \u201cextensive experience of its partners for the\u201d reliable execution of service experiments and custom production requests. Super-Long Read Sequencing Kit TELL-Seq\u2122 Kit from Universal Sequencing Technology enables the construction of NGS libraries with 200Kb fragments that can be sequenced with Illumina instruments. 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