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Gene finding
Gene finding with similarity
Gene finding in Bacteria
Gene finding in Viruses
Next Generation
Gene search
Gene explorer
Protein location
RNA structure
Protein structure
Multiple alignment
Analysis of expression data
Plant promoter database
Search and map repeats
Extracting known SNPs



Analyze RNASeq Next Generation Sequencing Data:

- Accurate alignment of high-throughput RNA-seq data to a reference genome (ReadsMap);

- De novo transcriptome reads assembly into RNA transcripts (TransSeq - Program for assembling transcripts from short reads.);

Transomics - pipeline to map RNAseq data, assemble them into transcripts and quantify the abundance of these transcripts in particular datasets.

Analyze Genomic Next Generation Sequencing Data:

- OligoZip Assembler - De novo reconstruction (assembling) of genomic sequence,

- Reconstruction of sequence using reference genome,

- Mutation profiling and SNP discovery.

- Functional analysis of SNP (SNP-effect);

The GenomeMatch pipeline is developed to find alignments between genome sequences as well as to construct synteny maps.

GenomeMatchViewer uses output of GenomeMatch alignment program to visualize similarity of genome sequences


3D-explorer trial version

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3D-Explorer is designed to visualize spatial models of biological macromolecules and their complexes. The 3D-Explorer application is compatible with PDB files. 3D-Explorer has an interface compatible with the GetAtoms and CE applications.





Seltag trial version

[Download and Instruction] [Help] [See more pictures here]
SelTag is one of the most elegant tools for analysis of expression data. It can analyze all or marked groups of genes or tissues, select tissue-specific genes based on complex criteria, provide visual representation of expression data.





[Download and Instruction]  [Help (draft)] [See more pictures here]
Genome Comparison Browser (GCB) is designed to visualize comparison of two genomes or chromosomes.

GCB main window

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