Next Generation Sequencing (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.

Identification of mutations associated to Myelodysplasic Syndroms, Myeloproliferative Neoplasms and Leukemia.

High quality results with the eleven-loci multiplex

Speed up your NGS workflow with the six-loci multiplex

Chimerism monitoring by NGS

Non-invasive preimplantation chromosome screening technique.

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

PGT-A (Preimplantation Genetic Testing for Aneuploidies) solution, that combines WGA and library preparation for NGS (MALBAC® technology).

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

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

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

Solution for the Whole Genome Sequencing of any bacterium or isolated organism.

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 42 genes involved in the in the most common solid tumors: lung, colorectal, skin, and brain cancers

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…

Genetic diagnostic test for sudden cardiac death and familial heart disease.

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 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…

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

Study of the coding regions of more than 19,000 genes by NGS.

Study of over 560 genes related to common hereditary diseases.

Study of the 44 most clinically relevant genes related to nephropathies.

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).

Study of genes associated with heart diseases.