Interactive Biosoftware

Alamut - Mutation Interpretation Software

AlamutAre you a molecular biologist studying human DNA sequence variations? Alamut is tailor-made for you.


Learn more about Alamut...

Canova - CNV Analysis

Canova helps analyzing copy number variations detected in array CGH experiments.
This prototype web tool is freely available here.

Genetic Literature Text Mining

Alamut uses Talamut, a search engine dedicated to genetic mutations cited in PubMed. You can try it here.

You can also try our experimental tool Correl: it displays graphs of correlated genes, based on statistical frequencies of co-occurrent terms in literature.

GeneSplicer

GeneSplicerWe have compiled GeneSplicer, a system for detecting splice sites, for Windows and Mac OS X. The full package is available here.

EMBOSSWin

EMBOSSWin thumbnail

EMBOSSWin is a Windows port of EMBOSS, a free Open Source software analysis package specially developed for the needs of the molecular biology user community.

EMBOSSWin is available here.

A Python ABIF (.ab1/.fsa) file reader

Python-PoweredIf you need to read trace files from Applied sequencers (".ab1" files), or fragment analysis files (".fsa" files), in Python, you can freely use this code. It is released under the GNU General Public License.

ABIFReader.py is available here.