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An R package for analyzing large Affymetrix data sets.
A comprehensive design and analysis tool for setting up and interpreting your microarray experiments.
Software for a complete CGH and CGH+SNP microarray data analysis and data reporting solution to streamline the day-to-day cytogenetic sample analysis research workflow.
A web tool for the analysis of aCGH data sets. They focus on calling gains and losses and estimating the number of copy changes. Note: ADaCGH will continue being maintained, but is deprecated. Their new tool for CGH and CNV is WaviCGH, http://wavi.bioinfo.cnio.es/
A software tool for the normalization, visualization, breakpoint detection, and comparative analysis of array-CGH data which allows the accurate and sensitive detection of CNAs.
A suite of distributed software applications for aligning short DNA reads, and manipulating and analyzing short read alignments.
A software suite including a scalable hierarchical multitasking parallel infrastructure and the classical sequencing algorithms.
A short string alignment package whose goal is to provide an all-inclusive set of tools to handle short (NGS-like) reads.
A new parallel read-mapping algorithm optimized for mapping next-generation sequence data to the human genome and other reference genomes, for use in a variety of biological analyses including SNP discovery, genotyping, and personal genomics.
Software for aligning sequencing reads against large reference genome. Consists of three algorithms: BWA-backtrack, BWA-SW and BWA-MEM. First for sequence reads up to 100bp, and other two for longer sequences ranged from 70bp to 1Mbp.
A generic web-based system, providing statistical methodology and computing power to handle a variety of biological inquires on genomic datasets.
Tool that facilitates the design and optimization of gene-specific DNA methylation assays. Beyond its use as an epigenetic primer-design tool, it provides extensive support for epigenetic biomarker optimization. Download MethMarker or start it directly from within your web browser.
You can easily align, visualize and quantify bisulfite sequence data for CpG methylation analysis.
Improved mapper for bisulfite sequencing reads on DNA methylation.
An approach for the analysis of two-base encoding bisulfite sequencing data.
A high-efficiency and easy-to-use analysis pipeline for MeRIP-Seq peak-finding at high resolution, which compares distributions of reads between immunoprecipitation sample and control sample.
A peak-caller for CLIP- and RIP-Seq data. It takes input in BED or BAM format and identifies regions of significant read enrichment. Additional covariates may optionally be provided to further inform the peak-calling process., THIS RESOURCE IS NO LONGER IN SERVICE. Documented on September 16,2025.
A hidden Markov model (HMM)-based software to predict clusters RNA motif sites.
A public database that provides the complete transcription factor (TF) repertoires of 6 genome sequenced tree species: papaya (Carica papaya), jatoropha (Jatropha curcas), cassava (Manihot esculenta), poplar (Populus trichocarpa), castor bean (Ricinus communis) and grape vine (Vitis vinifera). from annotated genes on each genome.
A Knowledge Database of Soybean Transcription Factors. PSI-BLAST is available to find hits from the database.