Blast2GO® is an ALL in ONE tool for functional annotation of (novel) sequences and the analysis of annotation data.
Paintomics is a web tool for the integration and visualization of transcriptomics and metabolomics data.
Currently Paintomics supports integrated visualization of about one hundred top species of different biological kingdoms and offers user the possibility to request any other organism present in the KEGG database.
Qualimap is a platform-independent application written in Java and R that provides both a Graphical User Inteface (GUI) and a command-line interface to facilitate the quality control of alignment sequencing data.
maSigPro is a statistical procedure to identify genes that show different gene expression profiles across analytical groups in time-course experiments.
The method has been implemented in the statistical language R and is freely available from the Bioconductor contributed packages repository
NOISeq is a non-parametric approach for the identification of differentially expressed genes from count data or previously normalized count data. NOISeq empirically models the noise distribution of count changes by contrasting fold-change differences (M) and absolute expression differences (D) for all the features in samples within the same condition.
NOISeq is available as a package in Bioconductor.
The STATegraEMS is an Experiment Management System (EMS) designed for storage and annotation of complex NGS and omics experiments. The STATegraEMS supports different types of sequencing-based assays, proteomics and metabolomics data.
SQANTI is an automated pipeline for the classification and quality-control evaluation of long-read transcriptomes. SQANTI allows the user to maximize the analytical outcome of long read technologies as PacBio by providing the tools to deliver quality-evaluated and curated full-length transcriptomes.
spongeScan is a web tool designed to identify and visualize lncRNAs acting as putative miRNA sponges, by searching for multiple miRNA binding sites in lncRNAs.
RGmatch is a flexible and easy-to-use tool to match genomic regions to the closest gene (also transcript or exon), which provides the area of the gene where the region overlaps. The algorithm can be applied to any organism as long as the genome annotation is available.
We are the INB Valencia Node
Genomics of Gene Expression Lab.
Príncipe Felipe Research Center
C/ Eduardo Primo Yúfera 3
Valencia 46012, Spain
Tel. +34 963 289 681 Ext. 3019
Fax. +34 963 289 701