Showing 14865 open source projects for "engineering"

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  • 1

    SODE

    Program to solve differential equations using long Taylor series

    Program to generate a program to numerically solve either a single ordinary differential equation or a system of them.It is a Ruby program, now called omnisode, which generates either Ruby, C, C++, Maple or Maxima code. Code can be generated for all languages under Linux. Ruby can be generated under Windows. All can be generated under cygwin, but would need work on execution of Maple. Omnisode itself is Ruby, which is needed in all cases to generate the program.
    Downloads: 4 This Week
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  • 2
    GNAT

    GNAT

    GNAT recognizes gene names in text and maps them to NCBI Entrez Gene

    GNAT is a BioNLP/text mining tool to recognize and identify gene/protein names in natural language text. It will detect mentions of genes in text, such as PubMed/Medline abstracts, and disambiguate them to remove false positives and map them to the correct entry in the NCBI Entrez Gene database by gene ID. March 2017: We started to upload GNAT output on Medline. See files/results/medline/.
    Downloads: 0 This Week
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  • 3
    FUMOLA - Functional Mock-up Laboratory

    FUMOLA - Functional Mock-up Laboratory

    An FMI-based co-simulation framework.

    FUMOLA is a co-simulation framework specifically designed to support the features offered by the FMI specification. It provides a flexible platform that allows to configure and execute co-simulation setups in an easy way. FUMOLA is developed on top of the Ptolemy II framework (https://ptolemy.eecs.berkeley.edu) and the FMI++ library (http://fmipp.sourceforge.net). The online documentation of FUMOLA is available here: https://sourceforge.net/p/fumola/wiki/Home/
    Downloads: 0 This Week
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  • 4
    A utility for processing command line arguments
    Downloads: 0 This Week
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  • 5
    isiKnock

    isiKnock

    In silico knockouts for signaling pathways

    Signaling pathways are complex and intertwined processes. The perturbation of biological systems can reveal the complicated interplay and dependencies of pathway components. isiKnock is a software to automatically conduct and visualize in silico knockouts for signaling pathways (Hannig et al. 2019). isiKnock predicts the knockout behavior based on the calculation of signal flows at steady state. For an explanation of the concept of in silico knockouts, we refer to Scheidel et al. 2016...
    Downloads: 0 This Week
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  • 6

    PanOCT

    Pan-genome Ortholog Clustering Tool

    PanOCT, Pan-genome Ortholog Clustering Tool, is a program written in PERL for pan-genomic analysis of closely related prokaryotic species or strains. Unlike traditional graph-based ortholog detection programs, it uses micro synteny or conserved gene neighborhood (CGN) in addition to homology to accurately place proteins into orthologous clusters.
    Downloads: 2 This Week
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  • 7
    PangInput

    PangInput

    A simple tool for typing characters in different writing systems.

    PangInput is a simple application to help you in typing characters from different languages in unicode. Three methods are available: 1) a virtual keyboard, mapping specific characters to each key on your keyboard; 2) custom character sets, which you can select by clicking on them; 3) macro sets, allowing input of complex scripts - basically mapping a latin transcription to the actual writing of characters or words.
    Downloads: 0 This Week
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  • 8
    Pootle Django

    Pootle Django

    Online translation tool

    Pootle is written in Python using the Django framework and therefore can be installed on any web server that supports serving WSGI applications. Key localization file formats are supported, including Gettext PO, XLIFF, Java .properties, PHP arrays and many more supported by the Translate Toolkit. Ensures the best quality localizations by automatically detecting common errors made by translators. Integrates user suggestions, terminology, Translation Memory, Machine Translation, and more. A...
    Downloads: 0 This Week
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  • 9

    CNVMM

    CNVMM performs copy number variations detection

    CNVMM specializes in identifying copy number variations (CNVs) when there are repeated sequences in the reference genome. The input file is a single short read mapping result from any short read aligners. However, NNmapper or Bowtie2, which detect all mapping results for multi-reads, are recommended. To use the code, MATLAB installation is required. Mac or Linus system is required.
    Downloads: 0 This Week
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  • 10

    libbencl

    OpenCL wrapper to use with the gloost framework

    Downloads: 0 This Week
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  • 11
    Mathematica-SPICE

    Mathematica-SPICE

    Call SPICE from Mathematica to enable advanced circuit optimization

    This project connects the ubiquitous circuit simulation software, SPICE, with the powerful tools of Mathematica. This allows the optimization of circuits based on arbitrarily complex criteria. For example, automatically tune component values to match a desired filter profile. Tweak a circuit to maximize its efficiency. Match a circuit's output to an arbitrary waveform. As long as you can quantify your goal as a fitness function, you can automate the search for the optimal component specs.
    Downloads: 1 This Week
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  • 12

    NNmapper

    Perform short reads mapping

    NNmapper constructs reference reads library and calculates the Euclidean distances between library reads and query reads. NNmapper can map a query read (1) to the library read that gives the smallest distance (most similar), (2) to the library read that gives the smallest distance while the distance is smaller than a threshold, or (3) all library reads that have distances smaller than threshold. NNmapper has high error-tolerant and is suitable for any read lengths. NN reports all mapping...
    Downloads: 0 This Week
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  • 13
    CoSMoSim

    CoSMoSim

    Visual & persistent families of models for CA, DEVS, and Statecharts

    CoSMoSim offers an integrated framework for model development, simulation, & experimentation. Its unified logical, visual, and persistence framework supports specifying families of parallel CA, DEVS, Statecharts, and XML-Schema models (see DEVS-Suite simulator).
    Downloads: 0 This Week
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  • 14
    BWA is a program for aligning sequencing reads against a large reference genome (e.g. human genome). It has two major components, one for read shorter than 150bp and the other for longer reads.
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    Downloads: 181 This Week
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  • 15
    Fcalgs is a collection of standalone tools implementing algorithms for formal concept analysis.
    Downloads: 0 This Week
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  • 16

    Nutrition Tables

    Nutrition Investigator

    This Nutrition Software consists of easy modifiable tables of selected food nutrients in one file, helps to make an individual diet. The information in this file was obtained from: Source (or Adapted from, as appropriate): Canadian Nutrient File, Health Canada, 2010 and other sources. This file gives an idea of which nutrient could be more likely found in fair quantities in some product. Use that file as a reference tool. Do not make any diet plans based on this information only,...
    Downloads: 0 This Week
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  • 17

    CNCLib

    CNC Interpreter for Arduino

    the project was moved to: https://github.com/aiten/CNCLib see also https://sourceforge.net/projects/cncstepper/ Windows (see download:CNCLib, use .net 4.6.1) * Sending (GCode) to Arduino * Support different machines (axis, range, ...) * Support CNC-Joystick(Arduino based) * Preview * Import HPGL with "Resize" and "Move" * Import Image (laser) * Sample for WPF, WebApi, Enterprise architecture, ... Windows (see download:Plotter) * Sending (HPGL) to Arduino sample sketch...
    Downloads: 0 This Week
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  • 18

    MethyMer

    Design of specific primer combinations for bisulfite sequencing

    MethyMer is a Python-based tool aimed at selecting specific primers for amplification of complete CpG islands. These regions are difficult in terms of selection appropriate primers because of their low-complexity, polyN-, CG-richness, etc. MethyMer have a flexible scoring system capable of selecting primers in problematic regions (e.g. SpG islands) and includes specificity test (based on bowtie alignment against bisulfite-treated genome). It also incorporates TCGA CpG methylation...
    Downloads: 0 This Week
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  • 19

    ATOMKI Common Data Acquisition

    Nuclear physics data acquisition system

    Nuclear physics data acquisition system. The suit of applications can be used to collect data from physics experiments using CAMAC/CAEN/VME devices. The system is quite specialized, but the code can still be useful for others doing something similar...
    Downloads: 0 This Week
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  • 20

    Arithmetic App

    Math App for kids

    This iapp is used by kids to help primary school kids improve their math skill by asking them math questions based on level
    Downloads: 0 This Week
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  • 21
    Downloads: 3 This Week
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  • 22

    salomebinaries

    Binary files of Salome-Platform

    Version of Salome, tested with CalculiX Launcher: http://www.calculixforwin.com/
    Downloads: 1 This Week
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  • 23
    SciPy: Scientific Library for Python
    NOTE: the project has moved to https://scipy.org/scipylib/ --- go there to find latest versions. This sourceforge project contains only old historical versions of the software. SciPy is package of tools for science and engineering for Python. It includes modules for statistics, optimization, integration, linear algebra, Fourier transforms, signal and image processing, ODE solvers, and more.
    Downloads: 7 This Week
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  • 24

    RNAfdl

    RNA force directed layout

    RNAfdl is a highly flexible tool for drawing RNA secondary structures. Secondary structures can be visualized as classical secondary structure plot, circle plot, linear plot or mountain plot. RNAfdl allows manual editing and several drawing styles, as well as a fully automated conjugate gradients minimization approach to draw more complex structures without user interaction. In addition, RNAfdl allows you to incorporate non-canonical base pairs into drawings.
    Downloads: 0 This Week
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  • 25

    mfsizes

    Multi-FASTA sequence (DNA or protein) statistics calculator.

    A simple command-line utility to calculate biological sequence (DNA or protein) sizes in a (multi) FASTA file. It gives averages, GC (or methionine) content, N50, N90, N95, number of N's, and total bases, and can also report by codon if requested.
    Downloads: 0 This Week
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