We support boolean queries, use +,-,<,>,~,* to alter the weighting of terms
Database for exploration of single cell RNA sequencing experiments from mouse and human. Collects and integrate data from multiple studies and present them through unified framework.
Software package to provide functions richGO, richKEGG,and enrich to do functional enrichment analysis. Used for function enrichment analysis and network construction.
Software R package to detect gene level differential selection between two groups of samples.Used for calculation of excess of non synonymous mutations between two groups.
Software platform to integrate transcription factor gene interactions and validate regulatory networks. Gene regulatory network validation.
Software platform to support systems biology research. Integrates genomic data and provides visualization and analysis tools for exploration of genomic data. Provides tools to generate biological hypotheses.
Software R package providing missing functionality to ggplot2 through extension system introduced with ggplot2 v2.0.0.
Software R package to format data, frame column names, provide quick counts of variable combinations and isolate duplicate records, format tabulation results.
Software Python package to perform post-processing of cryo-EM maps. Deep learning model trained on pairs of experimental volumes and atomic model corrected volumes that is able to obtain post-processed maps using as input raw volumes, preferably half maps.
Software tool as multiple sequence alignment formulated as statistical machine learning problem, where optimal profile hidden Markov model for potentially very large family of protein sequences is searched and alignment is decoded.
Web server for systematically predicting sequence regulatory activities and applying sequence information to human genetics data. Provides global map from any sequence to regulatory activities, as represented by sequence classes, and each sequence class integrates predictions for chromatin profiles like transcription factor, histone marks, and chromatin accessibility profiles across wide range of cell types.
Open source software suite for analysis of fiber photometry data.
Platform to let you gather data from across NCBI databases. Allows to find and download gene, transcript, protein and genome sequences, annotation and metadata.
LED illuminator for BX53 is equivalent to or better than 100 W halogen lamp, delivering brightness appropriate for teaching or contrast methods. Can be customized for different observation methods, such as phase contrast and fluorescence, with modular components.
Software tool for comprehensive conversion of folder with Hypnodyne zmax EDF files into merged European Data Format.
Primary access point for compendium of LINCS data with substantial changes in data architecture and APIs, completely redesigned user interface, and enhanced curated metadata annotations to support more advanced, intuitive and deeper querying, exploration and analysis capabilities. LINCS datasets are accessible at data point level enabling users to directly access and download any subset of signatures across entire library independent from originating source, project or assay. Newly designed query interface enables global metadata search with autosuggest across all annotations associated with perturbations, model systems, and signatures.
Supports research that requires comprehensive assessment of energy balance and body composition in experimental rodents by providing necessary equipment and expertise. Services include training in the use of equipment, consultation on experiment design, and help with data analysis. Instrumentation includes Bruker TD-NMR LF100 Minispec and TSE Phenomaster System with Integrated Stellar Telemetry.
Web service to predict molecular interactions that may occur between target protein and small molecule. Protein small molecule docking web service based on EADock DSS.
Computerized morbidity registration network in Belgium based on general practice data.Contains demographic, clinical, biomedical, and prescription data, registered with computer generated keywords in electronic health record.
Software tool for calculating average nucleotide identity.
Software tool that calculates distances between BGCs in order to map BGC diversity onto sequence similarity networks, which are then processed for automated reconstruction of Gene Cluster Families, groups of gene clusters that encode biosynthesis of highly similar or identical molecules.