191. LSHTM library - Genetic epidemiology library from London School of Hygiene and Tropical Medicine.
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192. LSID (Life Science Identifier) - Life Science Identifier (LSID) resolution protocol, to locate biologically significant data over a network, within middle-ware providing a client A.P.I. for Life Science applications, and server software, for Industry data providers.
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193. Mac Audiometrie - Freeware dedicated to surdity
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194. Madeline 2.0 Pedigree Drawing Engine - The Madeline 2.0 Pedigree Drawing Engine is a pedigree drawing program designed to handle large and complex pedigrees with an emphasis on readability and aesthetics.
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195. Manuelito - Manuelito is a Java tool for decrypting posttranslational modification (PTM) patterns of proteins based on MALDI mass spectrometry spectra. It was built for analysing the 'histone code' but it can be applied to any other highly modified protein.
Click here to download. | Rank/Activity Percentile
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196. MARiS: Radiological OpenSource Project - The project is based on the experience carried out in the University of Padova where at the end of 1997 we have choose to create one Computer science Unit inside of Department of Medical and Sciences and Special Therapies to develope Radiological OSS.
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197. MASyV - MASyV (Multi-Agent System Visualization) enables one to write agent-based models/cellular automata, eg. in C, visualize them in real time & capture to movie file with MASyVs GUI & message passing lib. Includes examples: Hello World, ants, viral infection
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198. MatchingPursuit - Our goal is to surpass the performance of the Matching Pursuit and Best Basis algorithms and provide progressive time-frequency
analysis.
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199. matNMR - MatNMR is a highly flexible toolbox for processing 1D and 2D NMR/EPR spectra in MATLAB and creating high-quality 1D, 2D or 3D plots. Fully GUI and/or script-based.
Click here to download. | Rank/Activity Percentile
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200. Mauve - Mauve computes and interactively visualizes genome sequence comparisons. Using FastA or GenBank sequence data, Mauve constructs multiple genome alignments that identify large-scale rearrangement, gene gain, gene loss, indels, and nucleotide substutition
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