Next Generation Sequencing (NGS)

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).

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

Non-invasive preimplantation chromosome screening technique.

High quality results with the eleven-loci multiplex

NGS kit for chimerism assessment

Kit for NGS sequencing of 17 genes that may impact the outcomes in transplantation

Kit for the relative quantitation, using plasma, of the donor derived cell free DNA, a great biomarker in the transplant follow-up.

Study of genes associated with heart diseases.

Study of genes associated with heart diseases.

Study of 54 genes associated with different types of lymphomas.

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

Study of 4 genes associated with breast and ovarian cancer.

Analysis of 4,728 genes related to rare and hereditary disorders.

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