Next Generation Sequencing (NGS)

Next-generation sequencing kit for the comprehensive analysis of genes associated with familial hypercholesterolemia, including a polygenic risk score and a SNP panel for statin response. Detailed Description Operating Principle The Devyser FH kit is an amplicon-based NGS library preparation solution with a single-tube protocol that enables targeted amplification and sample indexing within a streamlined workflow.…

Comprehensive solution for whole exome sequencing with Illumina technology, combining library preparation by tagmentation with capture-based enrichment, sequencing, and bioinformatics analysis, enabling a single workflow. Detailed Description Operating Principle The workflow uses magnetic bead-linked transposomes (eBLT) for rapid and uniform tagmentation. Following index PCR, a hybrid capture enrichment step is performed using the Twist Bioscience…

Solutions for the study of genetic alterations associated with different hereditary cancer predisposition syndromes, based on next-generation sequencing and automated analysis using the SOPHiA DDM™ software. Detailed Description SOPHiA GENETICS™️ solutions for hereditary cancer use capture-based NGS technology to achieve uniform coverage of target regions and high on-target rates. The analytical workflow relies on SOPHiA…

Operating Principle: The Devyser CFTR NGS kit redefines the genetic diagnosis of cystic fibrosis by offering a comprehensive and precise solution, validated for clinical use. With a unique single-tube library preparation approach, this kit optimizes the CFTR gene analysis process, significantly reducing hands-on time and contamination risk while improving diagnostic accuracy. Clinical Applications Advances in…

IVDR workflow for whole exome sequencing (WES) that integrates Twist's exclusive double-stranded DNA (dsDNA) probe technology with its library preparation and targeted capture reagents. The result: achieving the best coverage uniformity on the market and superior quality data for clinical environments. Detailed Description Operating Principle The system combines a streamlined library preparation, based on single-tube…

Introduction The SRSLY NGS Library Prep Kit from ClaretBio offers an efficient and simplified solution for library preparation using a technology based on single-stranded DNA through a ligation method. Unlike traditional library preparations, which are based on double-stranded DNA, SRSLY kits allow the entire DNA of the initial sample to be transformed into a sequenceable…

The Oncodeep kit from OncoDNA offers a comprehensive solution for identifying mutations, variants, and fusions in the somatic line of genes associated with solid tumors through Next-Generation Sequencing (NGS). Designed by oncology experts, this kit includes the most relevant and complete gene panel in the field of cancer, consisting of 638 genes, which allows for…

NGS panel for the study of 23 key genes associated with Chronic Lymphocytic Leukemia (CLL), including the biomarkers outlined in international guidelines (TP53 and somatic hypermutation).

NGS panel for the study of 23 key genes associated with Chronic Lymphocytic Leukemia (CLL), including the biomarkers outlined in international guidelines (TP53 and somatic hypermutation).

NGS assay for the analysis of 32 genes associated with common solid tumors from circulating tumor DNA (ctDNA)

Twist Human Comprehensive Exome and Twist Human Exome 2.0+ are two of the capture solutions for human exome sequencing from Twist Bioscience. The combination of Twist's proprietary double-stranded DNA (dsDNA) probes and its library preparation and capture reagents achieves the best market uniformity of coverage and the lowest duplicate rate, generating the highest quality data…

NGS capture kit to identify strains of more than 200 known and new coronaviruses for genomic surveillance.

NGS Kit for the depletion of human and microbial ribosomal RNA (23s, 5s and 16s) for subsequent application in metatranscriptomics.

NGS capture kit to detect and characterize the 40 most common respiratory DNA and RNA viruses, including SARS-Cov2 variants.

NGS capture kit to identify more than 280 respiratory pathogens, including DNA and RNA viruses, bacteria and fungi. In addition, more than 1200 antimicrobial resistance (AMR) alleles are analyzed.

NGS capture kit to identify the 66 viruses identified by public health as high health risk.

NGS Shotgun sequencing is a laboratory technique for determining one or more DNA sequences from the genome of an organism or an entire sample. The method consists of breaking the genome into a collection of small DNA fragments that are arranged individually. The individual fragments must then be bioinformatically placed in the correct order to…

Analysis of ITS1 regions for the characterization of fungi

Analysis and interpretation for the study of the V3 and V4 hypervariable regions of the 16S gene.

NGS capture kit for the detection of 3,153 viruses, including 15,488 different strains..

Robot for the generation of high-quality ForenSeq libraries, minimising errors and hands-on time. Ahorra recursos y minimiza los errores humanos con la PrepStation de Verogen. Esta plataforma, diseñada y validada Free up resources and minimise human error with the Verogen PrepStation. Designed and validated specifically for semi-automated MPS (Massive Parallel Sequencing) library preparation with ForenSeq…

NGS capture kit that allows detection and quantification of more than 170 organisms, including common and rare main uropathogens. In addition, it includes the detection of more than 3,700 antimicrobial resistance markers. UPIP is a NGS research panel that brings the power of precision metagenomics to the identification of genitourinary pathogens. This capture kit that…

NGS-based solution for identification, genotyping and prediction of drug resistance of Mycobacterium tuberculosis

Convenient and cost-effective library prep for sequencing the whole mitochondrial genome with minimal DNA input and exceptional data recovery.

Convenient and efficient library prep for interrogating the control region of the mitochondrial genome with minimal DNA input and optimum sensitivity.

Chimerism monitoring by NGS

La prueba más completa para determinar el estado de deficiencia de la recombinación homóloga (HDR) estudiando los genes BRCA y 13 más adicionales, en pacientes con cáncer de ovario.

The most comprehensive tumor test to determine Homologous Recombination Deficiency (HDR) Status by studying the BRCA genes in patients with ovarian cancer.

Twist Human Core Exome and Twist Human Core Exome + Ref Seq are the two capture solutions for human exome sequencing by Twist Bioscience. The superior performance of the Twist Core Exome provides the optimal solution for sequencing human coding genes, while focusing on the most accurate curated subset of genes: that of the CCDS…

Endometrial Receptivity Test to improve the clinical pregnancy of IVF-ET (In vitro Fertilization & Embryo Transfer).