If you already have the data, we start from there. We analyze raw sequencing data, expression tables or results from other platforms, reuse public data to validate or extend your findings, and combine several omics layers to answer your question.
Whatever stage of the process they are at, we pick up the analysis from the format you have.
Sequencing reads or instrument files straight from the platform. We handle quality control and all processing.
Count matrices, abundance tables or results from another provider that need deeper analysis or a second opinion.
Published studies in international repositories that can be reanalyzed with your question in mind.
We work with data from every omics layer, from whole tissue or single cells.
mRNA-seq, Total RNA-seq, lncRNA, circRNA, small RNA and Iso-Seq.
scRNA-seq, snRNA-seq, TCR/BCR and spatial data.
WGS and WES, variants, CNVs and genome assembly.
DNA methylation, ChIP-seq and RIP-seq.
16S/18S/ITS amplicons, shotgun and metatranscriptomics.
Olink (NPX) and mass spectrometry data.
Untargeted LC-MS: detection, annotation and statistics.
Clinical and phenotypic variables to integrate with the omics.
Thousands of published omics studies have accessible data. Properly reanalyzed, they add a lot of value, especially when your own samples are few.
Each omics layer tells part of the story. Integrating them shows how a change in the genome or in expression translates into proteins and metabolites.
A review of your starting data before analysis, so you know what questions they can answer.
Differential expression, pathways, networks or integration, depending on your question.
Plots ready for a paper, report or committee.
What the results mean and what the next steps are.
Access to our software to explore the results without coding: search any gene or protein, compare groups and build interactive plots.
Tell us what data you have and what you want to answer. We will tell you what can be obtained from them and send you a proposal.