We support boolean queries, use +,-,<,>,~,* to alter the weighting of terms
Software for accurate and sensitive CNV discovery and genotyping in long-range targeted resequencing.
Software that implements a computational model for predicting immunosuppressive domains (ISDs). The software could be used to identify typical ISDs in retroviruses including HERV, HTLV, HIV, STLV, SIV and MLV.
An intuitive and flexible software tool for building and displaying glycan structures.
A software package for automated recognition of glycans from LC/MS data.
Software for the conversion of data acquired with the FlashQuant (MALDI version of ABSciex 4000) into MS images.
An open source Java application that provides a clear and concise analysis workbench for large amounts of cell motion data.
An adaptive imaging cytometry software environment.
Software that annotates biologically functional gene fusion candidates.
A web application creating Venn diagrams from two or three gene lists.
Software for a low frequency Virus Variant detection pipeline for Illumina data.
Software tool to pick out ion signals that discriminate two groups of samples (e.g. diseased/healthy, resistant/susceptible) by quasi-datapoint-wise comparison using univariate statistic procedures.
A user-friendly software tool to estimate allele-specific gene expression.
Software for an automated pipeline using a ''local mapping reference reconstruction method'' to revise mismapped or partially misaligned reads at simple tandem repeat loci.
Software for a highly automated bioinformatics pipeline to reconstruct and analyze human mitochondrial DNA from high throughput sequencing data.
Software tool for detecting identity-by-descent (IBD) tracts between pairs of genomic sequences.
An editing and visualization software tool for pathway models represented by the BioPAX format, using SBGN Process Description Language, based on Chisio.
Software that implements a HMM Model to detect copy number variants in exome sequence data.
A targeted gene assembly software program which aims to recover gene families of particular interest to biologists.
A software package for detecting INDELs (INsertions and DELetions) mutations in a reference genome which has been sequenced with next-generation sequencing technology (e.g., Illumina).