Services

Find out our services for the study of biomarkers across different areas of biomedical and basic research.

Find out our services

Platform for Direct Digital Molecular Detection

Our Nanostring nCounter MAX System analyzes hundreds of mRNAs, miRNAs, SNVs, CNVs or proteins through direct digital molecular detection, in a single reaction step and in the absence of enzymes (without the need for retrotranscription or amplification steps). This highly sensitive and reproducible system, with enhanced multiplexing capacity (up to 800 genes in the same reaction), not only reduces the number of reactions required, but also the amount of RNA/DNA sample required for the assay.

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Platform for Genome Sequencing, Transcriptomics and Data Analysis

The Illumina NextSeq2000 system features sequencing by synthesis (SBS) technology that tracks the addition of labeled nucleotides as the DNA chain is copied. This technology analyzes millions of fragments in massively parallel sequencing, improving the speed and accuracy of sequencing while reducing its cost.

The Illumina NextSeq 2000 Sequencing System features a novel super resolution optics system that yields highly accurate imaging data with greater resolution and higher sensitivity than traditional Illumina systems.

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Single CELL

What is Single Cell technology?

10x Genomics technology provides a betterreadout of cellular complexity from different perspectives - omics at the "single cell" level: the combination of information frommultiple omics layers -transcriptomics, proteomics and epigenomics- increasesthe power of the experiments.

NGSChromium X Single Cell Platform available in our NGSservice

Advantages of the 10x Genomics technology:

  • High-Throughput Single-Cell Sequencing
  • Thousands of cells per sample, which reduces the cost inhigh-throughput projects.
  • Multidimensional Single-Cell Data. Combination ofmultiple products to obtain single cell data in multiple dimensions.

Available options

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Bioinformatics Analysis

Generic

We provide omics data processing and debugging. We advise on pipeline assembly (standard and ad hoc) and custom software development.

DNA analysis

Processing of the entire DNA analysispipeline, from FastQ to variant annotation. Quality control at any point in theprocess.

Population structure analysis of samplegroups, identification of phenotype-associated markers and genes, functionalanalysis of pathways and data mining (search and processing) of databases inpublic repositories for alternative analyses.

RNA analysis

Expression analysis on RNA-Seq and Nanostringplatforms. Quality control, alignment and expression quantification at the geneor transcript level, and annotation.

Normalization and differential expression analysis and functional analysis of pathways.

Epigenomics

Data analysis using the Illumina Infinium Methylation 450K and EPIC BeadChip platforms: quality control, normalization and detection of differentially methylated positions (DMPs) and regions (DMRs)in different sample groups. Analysis of gene pathways associated with DMPs andDRMs.