{"id":27053,"date":"2026-04-13T07:46:08","date_gmt":"2026-04-13T07:46:08","guid":{"rendered":"https:\/\/www.dlongwood.com\/?post_type=productos&#038;p=27053"},"modified":"2026-04-13T07:46:08","modified_gmt":"2026-04-13T07:46:08","slug":"human-sample-id-kit-and-human-sample-id-mini-kit","status":"publish","type":"productos","link":"https:\/\/www.dlongwood.com\/en\/product-catalog\/human-sample-id-kit-and-human-sample-id-mini-kit\/","title":{"rendered":"Human Sample ID Kit and Human Sample ID mini Kit"},"content":{"rendered":"\n<!-- Bloque de Estilos Scoped (Aislados, Blindados y Escalados a 14px) -->\n<style>\n    \/* Importaci\u00f3n de fuentes corporativas *\/\n    @import url('https:\/\/fonts.googleapis.com\/css2?family=Playfair+Display:wght@400;700&family=Raleway:wght@300;400;500;600;700&display=swap');\n\n    \/* Contenedor Principal Aislado *\/\n    .dlw-prod-wrapper {\n        font-family: 'Raleway', sans-serif !important;\n        color: #000000 !important;\n        line-height: 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BLINDADO\n     ========================================== -->\n<div class=\"dlw-prod-wrapper\">\n\n    <!-- Descripci\u00f3n Corta (Lead Box) -->\n    <div class=\"dlw-lead-box\">\n        <p>NGS sequencing assay designed for independent sample identity confirmation in WES, WGS, and gene panel workflows, providing an additional layer of traceability and integrity control from sample receipt to final analysis. It generates a unique genetic fingerprint with a simple workflow and an automated report to facilitate data interpretation.<\/p>\n    <\/div>\n\n    <!-- Descripci\u00f3n Detallada -->\n    <h2>Detailed Description<\/h2>\n\n    <h3>Operating Principle<\/h3>\n    <div class=\"dlw-list\">\n        <span class=\"dlw-list-item\">The <em>sample tracking<\/em> kits are designed to create a <strong>unique genetic tag<\/strong> for each sample to facilitate identity verification.<\/span>\n        <span class=\"dlw-list-item\">The protocol is based on a single closed-tube PCR step, which simultaneously amplifies the targets and incorporates sample-specific dual indices.<\/span>\n        <span class=\"dlw-list-item\">Following pooling and a simple bead cleanup, the libraries are ready for sequencing, and the analysis is completed using associated software that generates a standardized report.<\/span>\n    <\/div>\n\n    <h3>Clinical Applications<\/h3>\n    <p>Its main interest in the clinical genetics laboratory lies in sample traceability and the prevention of identification errors in complex WES, WGS, and targeted panel workflows. These processes involve multiple chain-of-custody transfers, several analytical steps, and large volumes of data, which can compromise sample integrity throughout the process.<\/p>\n    <p>In this context, the kit provides an <strong>independent method to confirm that the sequenced sample actually corresponds to the expected patient<\/strong>. Sample mix-ups or swaps can occur in up to 3% of cases, reinforcing the utility of this type of control in laboratories needing to enhance the security of the analytical process.<\/p>\n\n    <h3>Benefits<\/h3>\n    <p>The product is designed to easily integrate into established workflows. The described advantages include ease of integration into WES and WGS, coverage uniformity, low DNA input requirement, and the availability of analysis software with standardized reporting.<\/p>\n    <p>It also stands out for its compatibility with high-quality DNA, FFPE samples, and cfDNA, which broadens its utility in laboratories handling different sample types within the same routine.<\/p>\n\n    <h3>Intended Audience \/ User<\/h3>\n    <p>Aimed at clinical genetics, genomics, molecular biology, and advanced diagnostic laboratories that need to strengthen traceability, identity verification, and sample quality control in next-generation sequencing workflows.<\/p>\n    <p>It is particularly relevant in environments involving multiple pre-analytical and analytical steps, or where samples of different origins and quality are processed simultaneously.<\/p>\n\n    <!-- Aspectos Clave -->\n    <h2>Key Features<\/h2>\n    \n    <div class=\"dlw-check-list\">\n        <div class=\"dlw-check-item\">\n            <svg class=\"dlw-check-icon\" viewBox=\"0 0 24 24\"><path d=\"M12 2C6.48 2 2 6.48 2 12s4.48 10 10 10 10-4.48 10-10S17.52 2 12 2zm-2 15l-5-5 1.41-1.41L10 14.17l7.59-7.59L19 8l-9 9z\"\/><\/svg>\n            <span><strong>Independent confirmation<\/strong> of sample identity for WES, WGS, and gene panel workflows.<\/span>\n        <\/div>\n        <div class=\"dlw-check-item\">\n            <svg class=\"dlw-check-icon\" viewBox=\"0 0 24 24\"><path d=\"M12 2C6.48 2 2 6.48 2 12s4.48 10 10 10 10-4.48 10-10S17.52 2 12 2zm-2 15l-5-5 1.41-1.41L10 14.17l7.59-7.59L19 8l-9 9z\"\/><\/svg>\n            <span><strong>Two assay types available<\/strong> depending on the needs:\n                <div class=\"dlw-sub-list\">\n                    <span class=\"dlw-sub-list-item\"><strong>Human Sample ID kit:<\/strong> based on 43 polymorphic SNPs and 6 sex markers, suitable for WES and WGS workflows.<\/span>\n                    <span class=\"dlw-sub-list-item\"><strong>Human Sample ID mini kit:<\/strong> based on 12 polymorphic SNPs and 1 sex marker, suitable for gene panels.<\/span>\n                <\/div>\n            <\/span>\n        <\/div>\n        <div class=\"dlw-check-item\">\n            <svg class=\"dlw-check-icon\" viewBox=\"0 0 24 24\"><path d=\"M12 2C6.48 2 2 6.48 2 12s4.48 10 10 10 10-4.48 10-10S17.52 2 12 2zm-2 15l-5-5 1.41-1.41L10 14.17l7.59-7.59L19 8l-9 9z\"\/><\/svg>\n            <span><strong>Simple workflow<\/strong> with a single closed-tube PCR and libraries ready for sequencing after a simple cleanup.<\/span>\n        <\/div>\n        <div class=\"dlw-check-item\">\n            <svg class=\"dlw-check-icon\" viewBox=\"0 0 24 24\"><path d=\"M12 2C6.48 2 2 6.48 2 12s4.48 10 10 10 10-4.48 10-10S17.52 2 12 2zm-2 15l-5-5 1.41-1.41L10 14.17l7.59-7.59L19 8l-9 9z\"\/><\/svg>\n            <span><strong>Compatible with diverse starting materials:<\/strong> high-quality genomic DNA, FFPE, and cfDNA.<\/span>\n        <\/div>\n        <div class=\"dlw-check-item\">\n            <svg class=\"dlw-check-icon\" viewBox=\"0 0 24 24\"><path d=\"M12 2C6.48 2 2 6.48 2 12s4.48 10 10 10 10-4.48 10-10S17.52 2 12 2zm-2 15l-5-5 1.41-1.41L10 14.17l7.59-7.59L19 8l-9 9z\"\/><\/svg>\n            <span><strong>Low DNA input and short workflow:<\/strong> 1\u201320 ng, 3 hours total time, and only 20 min hands-on time.<\/span>\n        <\/div>\n        <div class=\"dlw-check-item\">\n            <svg class=\"dlw-check-icon\" viewBox=\"0 0 24 24\"><path d=\"M12 2C6.48 2 2 6.48 2 12s4.48 10 10 10 10-4.48 10-10S17.52 2 12 2zm-2 15l-5-5 1.41-1.41L10 14.17l7.59-7.59L19 8l-9 9z\"\/><\/svg>\n            <span><strong>High discrimination power<\/strong>, suitable for differentiating samples and supporting the integrity of the analytical process.<\/span>\n        <\/div>\n        <div class=\"dlw-check-item\">\n            <svg class=\"dlw-check-icon\" viewBox=\"0 0 24 24\"><path d=\"M12 2C6.48 2 2 6.48 2 12s4.48 10 10 10 10-4.48 10-10S17.52 2 12 2zm-2 15l-5-5 1.41-1.41L10 14.17l7.59-7.59L19 8l-9 9z\"\/><\/svg>\n            <span><strong>Fully compatible<\/strong> with Illumina sequencing platforms.<\/span>\n        <\/div>\n        <div class=\"dlw-check-item\">\n            <svg class=\"dlw-check-icon\" viewBox=\"0 0 24 24\"><path d=\"M12 2C6.48 2 2 6.48 2 12s4.48 10 10 10 10-4.48 10-10S17.52 2 12 2zm-2 15l-5-5 1.41-1.41L10 14.17l7.59-7.59L19 8l-9 9z\"\/><\/svg>\n            <span><strong>Includes analysis software<\/strong> capable of generating a standardized results report.<\/span>\n        <\/div>\n    <\/div>\n\n    <!-- Detalles de Presentaci\u00f3n (Acordeones Desplegables) -->\n    <h2>Ordering Information<\/h2>\n    <p>The kit comes in a <strong>96-reaction<\/strong> format and two solutions are available, complemented by different sets of unique dual indices:<\/p>\n\n    <details class=\"dlw-accordion\">\n        <summary class=\"dlw-accordion-header\">Human Sample ID Kits<\/summary>\n        <div class=\"dlw-accordion-content\">\n            <table class=\"dlw-table\">\n                <tbody>\n                    <tr>\n                        <td width=\"30%\" class=\"dlw-ref-code\">PXL-SID-001<\/td>\n                        <td width=\"70%\">Human Sample ID Kit (96 rxn)<\/td>\n                    <\/tr>\n                    <tr>\n                        <td class=\"dlw-ref-code\">PXL-SID-002<\/td>\n                        <td>Human Sample ID mini Kit (96 rxn)<\/td>\n                    <\/tr>\n                <\/tbody>\n            <\/table>\n        <\/div>\n    <\/details>\n\n    <details class=\"dlw-accordion\">\n        <summary class=\"dlw-accordion-header\">Index Sets<\/summary>\n        <div class=\"dlw-accordion-content\">\n            <p style=\"margin-bottom: 1.5em !important; font-size: 1.1em !important; color: #555 !important;\"><em>Note: The different index kits are fully compatible with both solutions (ID Kit and ID mini Kit).<\/em><\/p>\n            <table class=\"dlw-table\">\n                <tbody>\n                    <tr>\n                        <td width=\"30%\" class=\"dlw-ref-code\">PXL-IND-003 to PXL-IND-009<\/td>\n                        <td width=\"70%\">Unique dual index sets (PXL-IND-003, PXL-IND-004, PXL-IND-005, PXL-IND-008, and PXL-IND-009)<\/td>\n                    <\/tr>\n                <\/tbody>\n            <\/table>\n        <\/div>\n    <\/details>\n\n<\/div>\n","protected":false},"excerpt":{"rendered":"<p>NGS sequencing assay designed for independent sample identity confirmation in WES, WGS, and gene panel workflows, providing an additional layer of traceability and integrity control from sample receipt to final analysis. It generates a unique genetic fingerprint with a simple workflow and an automated report to facilitate data interpretation. Detailed Description Operating Principle The sample [&hellip;]<\/p>\n","protected":false},"featured_media":27048,"template":"","tecnologias":[36],"marcas":[528],"familias":[454,297,426,445,455],"class_list":["post-27053","productos","type-productos","status-publish","has-post-thumbnail","hentry","tecnologias-next-generation-sequencing-ngs","marcas-pxlence-en","familias-sample-tracking-en","familias-exomes","familias-genomes","familias-hereditary_cancer","familias-sample-tracking-en-2"],"_links":{"self":[{"href":"https:\/\/www.dlongwood.com\/en\/wp-json\/wp\/v2\/productos\/27053","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/www.dlongwood.com\/en\/wp-json\/wp\/v2\/productos"}],"about":[{"href":"https:\/\/www.dlongwood.com\/en\/wp-json\/wp\/v2\/types\/productos"}],"version-history":[{"count":2,"href":"https:\/\/www.dlongwood.com\/en\/wp-json\/wp\/v2\/productos\/27053\/revisions"}],"predecessor-version":[{"id":27055,"href":"https:\/\/www.dlongwood.com\/en\/wp-json\/wp\/v2\/productos\/27053\/revisions\/27055"}],"wp:featuredmedia":[{"embeddable":true,"href":"https:\/\/www.dlongwood.com\/en\/wp-json\/wp\/v2\/media\/27048"}],"wp:attachment":[{"href":"https:\/\/www.dlongwood.com\/en\/wp-json\/wp\/v2\/media?parent=27053"}],"wp:term":[{"taxonomy":"tecnologias","embeddable":true,"href":"https:\/\/www.dlongwood.com\/en\/wp-json\/wp\/v2\/tecnologias?post=27053"},{"taxonomy":"marcas","embeddable":true,"href":"https:\/\/www.dlongwood.com\/en\/wp-json\/wp\/v2\/marcas?post=27053"},{"taxonomy":"familias","embeddable":true,"href":"https:\/\/www.dlongwood.com\/en\/wp-json\/wp\/v2\/familias?post=27053"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}