Illumina

Next‑generation sequencing (NGS) assay with hybrid capture enrichment for the detection and whole‑genome sequencing of approximately 200 RNA and DNA viruses relevant to public health. It integrates library preparation, enrichment, sequencing, and data analysis into an optimized workflow of about two days. Detailed Description Principle of operation The panel can start from RNA, DNA, or…

Targeted library preparation workflow for whole‑genome sequencing of influenza A and influenza B from total RNA on Illumina systems. Enables preparation of up to 48 libraries with unique dual indexes and generates sequencing‑ready libraries in less than 9 hours. Detailed Description Principle of operation The IMAP-Flu workflow uses a pool of 16 primers (Influenza A/B…

Amplicon-based NGS library preparation solution aimed at public health surveillance and microbiological research. Accepts DNA or RNA, as well as user-designed or commercial primers, with compatibility with multiple sample types and with almost all Illumina sequencing systems. Detailed Description Principle of operation Amplicon-based library preparation kit built on the same chemistry as COVIDSeq. The workflow…

Directed amplification and sequencing assay to recover and characterize the complete genome of respiratory syncytial virus (RSV) A and B from RNA extracted from positive respiratory samples, using reagents from the Illumina COVIDSeq assay. The provided documentation positions it as a solution oriented to viral surveillance, rapid genomic characterization, and analysis of respiratory samples with…

Next-generation sequencing (NGS) amplicon-based assay for the detection and characterization of SARS-CoV-2. It integrates library preparation, sequencing, and data analysis into a workflow aimed at genomic surveillance and is for research use only. 3.- Detailed Description Principle of operation Illumina COVIDSeq is integrated into a complete workflow for the detection and characterization of SARS-CoV-2, from…

NGS panel for hereditary cancer studies integrating the analysis of 113 clinically relevant genes with a rapid workflow and high coverage uniformity for the consistent detection of SNVs, indels, and CNVs. Detailed Description Operating Principle An end-to-end solution based on hybrid capture of 113 genes (all exons covered plus ±20 bp regions) and library preparation…

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…

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 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…

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