Showing 59 open source projects for "detect"

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  • 1

    janda

    structural variant detector

    Janda is a tool to detect structural variants in whole-genome DNA sequence data. It identifies structural variants (deletions, duplications, translocations, and inversions) using anomalously mapped pair reads and realigning potential junction reads.
    Downloads: 3 This Week
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  • 2
    JDiskMark

    JDiskMark

    Java Disk Benchmark Utility

    JDiskMark is a powerful and versatile disk benchmarking tool written in Java, designed to help accurately measure the performance of your storage devices across different operating systems. Whether you're testing HDDs, SSDs, or network drives, JDiskMark provides reliable insights into your disk's read and write...
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    Downloads: 14 This Week
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  • 3
    XBNF Neurotranslator compiler

    XBNF Neurotranslator compiler

    (X)BNF simple and clever translation grammar compiler

    XBNF Neurotranslator is a powerfull extended BNF grammar language to handle translations easily and many features to handle different kind of situations. This project is for common arch binaries, C++ sources, tests & support tickets. No installation, juste get binary for your architecture : > See [Files] > binary.{version} Library of smart samples of grammars> https://sourceforge.net/projects/xbnf/ Docker image which embeds the Linux/64bits binary and the...
    Downloads: 0 This Week
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  • 4
    iGPS

    iGPS

    An interactive tool for GNSS position time series analysis

    * Please check latest update on https://github.com/igps-ftk/iGPS A tool written in Interactive Data Language (IDL), for processing and analyzing daily continuous GPS position time series. It can read time series in various formats, detect outliers, remove abnormal observation spans, find jumps, extract common-mode components(CMC), etc.
    Downloads: 0 This Week
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  • 5

    Gait Measurement EMG Step Trigger

    Script to control step-triggered optogenetic pulse delivery.

    ...This script was developed and used in the laboratory of Veronique VanderHorst, MD PhD at Beth Israel Deaconess/Harvard Medical School. Specifically, this script was used to trigger pulses of light that were delivered to animals receiving optogenetic stimulation; the trigger was designed to detect the initiating of stepping by electromyographic activity that was recorded from the tibialis anterior. This script also activates a physical stopwatch at the initiation of data collection for purpose of synchronizing with video.
    Downloads: 0 This Week
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  • 6

    Gait Analysis Graphical User Interface

    Extracts gait parameters from 120 fps video of mouse walking

    ...This was developed and used in the laboratory of Veronique VanderHorst, MD PhD at Beth Israel Deaconess/Harvard Medical School. First, a GUI displays videos of mice walking on a custom apparatus and enables the user to manually detect paw position. This data is saved. Additional functions take this spatiotemporal information and extract commonly used gait parameters, which are then exported to a MATLAB structure to be used for scientific analysis.
    Downloads: 0 This Week
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  • 7
    Finding DNA Repeats by RFRE

    Finding DNA Repeats by RFRE

    RFRE is a tool to find DNA repeats (tandem and short)

    ...The Metacharcter and their behaviours in the context of regular expressions are the main methods to identify the different searched patterns and by different combination of Metacharcter, the programmed tool can search and detect the pattern of DNA sequence. Repeater Finder Regular Expression Tool Regular Expression for Protein Motif Search and SSR sequence. https://sourceforge.net/projects/rfret/files/RFRE122019.exe/download https://www.preprints.org/manuscript/201910.0249/v1 https://sites.google.com/must.edu.eg/finding-dna-repeats/home ---------------------------------------------- *****Very important program must be downloaded before you run the EXE FILE OF RFRE***** 1-VB6 Runtime Plus 2.2.exe , https://sourceforge.net/projects/vb6extendedruntime/
    Downloads: 0 This Week
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  • 8
    dataMAPPs

    dataMAPPs

    R based pipeline for MHC-associated peptide proteomics (MAPPs) data

    dataMAPPs allows routine and efficient processing of data from immunogenicity studies applying the MAPPs peptidomics technology to detect potential MHCI- or MHC-II epitopes as presented by dendritic cells (DC). It features quality control of the raw data, across-sample/across-donor normalization and visualization of results in a heatmap style (heatMAPPs). dataMAPPs' core is a generic R library that can be tailored to specific projects via dedicated control scripts which also allow reproducible recalculation of results. ...
    Downloads: 2 This Week
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  • 9
    PAMGUARD

    PAMGUARD

    Detection Classification and Localisation of marine mammals

    The PAMGUARD project develops software to help detect, locate and classify marine mammals using Passive Acoustic Monitoring. This project is being migrated to github at https://github.com/PAMGuard. Please go there for the latest updates. thank you sourceforge for hosting us for all these years.
    Downloads: 0 This Week
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  • 10

    AC Engine Calculator

    Calculate some attributes of an AC engine

    Engine Calculator is intended to solve 3 simple calculations: detect the frequency (Hertz), rotations per minute (RPM) and the number of poles of an alternated current motor. One of those may be found with the two others. I actually didn't found any bugs in this version (i.e typing the wrong value of a variable). This is my first app made completely by my own. <pt-br> Engine Calculator destina-se a resolver 3 cálculos simples: detectar a frequência (Hertz), rotações por minuto (RPM) e o número de pólos de um motor de corrente alternada. ...
    Downloads: 0 This Week
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  • 11
    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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  • 12
    ...Latest version uploaded in October 2017 has a bugfix for single treatment group normalization. Rescaling has been omitted from 2015. EigenMS utilizes SVD to detect bias trends in the data and eliminates them. EigenMS eliminates effects from known and unknown factors and can be utilized for any -omic platform. We have shown its utility in LC-MS/MS and metabolomics in the following two papers: 1) PMID: 19602524. "Normalization of peak intensities in bottom-up MS-based proteomics using singular value decomposition". ...
    Downloads: 0 This Week
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  • 13
    DataCleaner

    DataCleaner

    Data quality analysis, profiling, cleansing, duplicate detection +more

    DataCleaner is a data quality analysis application and a solution platform for DQ solutions. It's core is a strong data profiling engine, which is extensible and thereby adds data cleansing, transformations, enrichment, deduplication, matching and merging. Website: http://datacleaner.github.io
    Downloads: 11 This Week
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  • 14
    PyCosmic is a tool to detect and clean single images from the disturbing cosmic ray hits. It was designed and tested specifically for CALIFA and other fiber-fed integral-field spectroscopy dataset. It is written in Python and can be executed from the command line. New release is version v0.5. Updated to be compatible with numpy version 1.12. New release is version v0.4.
    Downloads: 0 This Week
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  • 15

    detectMITE

    Detection of Miniature Inverted Repeat Transposable Elements

    ... [1] Who are we? Please visit website: http://bioinfolab.miamioh.edu [2] How to cite detectMITE? Ye C, Ji G, Liang C (2016) detectMITE: A novel approach to detect miniature inverted repeat transposable elements in genomes. Sci. Rep. 6, 19688. http://www.nature.com/articles/srep19688 Ye C, Ji G, Li L, Liang C (2014) detectIR: A Novel Program for Detecting Perfect and Imperfect Inverted Repeats Using Complex Numbers and Vector Calculation. PLoS ONE 9(11): e113349. http://journals.plos.org/plosone/article?...
    Downloads: 1 This Week
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  • 16
    CloudMIG Xpress

    CloudMIG Xpress

    Find the best suited cloud provider and deployment for your software

    To reduce resource over and under-provisioning, software systems can be migrated to IaaS and PaaS-based cloud environments. However, aligning and optimizing existing software systems for a cloud computing foundation often involves substantial reengineering activities or at least an elaborated configuration during the migration. There exist various challenges that have to be addressed, for example, systematically comparing cloud environment candidates, checking the conformance with...
    Downloads: 0 This Week
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  • 17

    Discriminative Language Editor

    Discriminative language editor based on ontologies

    Text editor in Java that is able to detect discriminative expressions while the user is typing. When the internal ontology-based analyzer detects a potential discriminative expression the user is advised by underscoring the related words in the text. A descriptive message about the issue is also shown to the user when the cursor is placed over the potential discriminative expression.
    Downloads: 0 This Week
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  • 18

    REDO

    REDO - RNA Editing Detection in Organelle

    ...The stringent rule depended filters and statistical filters are used in REDO for reducing false positive rate. It can provide detailed annotations, statistics and figures for RNA editing sites. REDO also can detect RNA editing events in multiple samples simultaneously and identify differential proportion of RNA editing events in different samples. Moreover, the genome variation can be easily removed by a subprogram fish.pl in our package.
    Downloads: 0 This Week
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  • 19

    MULTOVL

    Multiple overlaps of genomic regions

    The MULTOVL suite of programs finds multiple overlaps among genomic regions. The MULTOVL algorithm can detect several kinds of region overlaps. In addition to the N-fold overlaps you can detect solitary regions which are the input regions that do not overlap with any other region in the input data set, and union overlaps that is the union of the input regions that overlap at least once somewhere. IMPORTANT NOTICE: MULTOVL has been migrated to BitBucket.
    Downloads: 0 This Week
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  • 20
    EricScript
    Ericscript is a computational framework to detect gene fusions from paired end RNA-seq data with high sensitity and specificity.
    Downloads: 0 This Week
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  • 21
    DNA patterns & application

    DNA patterns & application

    A software for generating DNA patterns

    The DNA pattern represents a new method of analysis for DNA sequences. In general it can easily detect relationships among species over the evolutionary landscape. Largely, in bioinformatics the DNA pattern method is unexplored and many discoveries can be made through it. One of the questions to which an answer was given is: How many types of promoters are out there regulating the genes ? It seems that there are 10 types of promoters.
    Downloads: 0 This Week
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  • 22
    riboFR-seq

    riboFR-seq

    A novel approach to linking 16S rRNA amplicon profiles to metagenomes

    ...Here we propose a novel approach, RiboFR-Seq (Ribosomal RNA gene Flanking Region Sequencing), for capturing both ribosomal RNA variable regions and their flanking protein-coding genes simultaneously. We demonstrated that RiboFR-Seq could detect the vast majority of bacteria not only in well-studied microbiomes but also in novel communities with limited reference genomes. Combined with classical amplicon sequencing and shotgun metagenome sequencing, RiboFR-Seq can link the annotations of 16S rRNA and metagenomic contigs to make a consensus classification.
    Downloads: 0 This Week
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  • 23

    PanCoreGen1

    A comprehensive tool to profile, detect & annotate microbial genomes.

    PanCoreGen is a Windows-based standalone tool offering 4-in-1 functionalities – (i) pan-/core-genomic profiles across the entire sample set; (ii) similar profiles within user-defined strain-groups; (iii) annotations of user-provided draft genomes; and (iv) detection of unidentified genes in annotated genomes.
    Downloads: 0 This Week
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  • 24

    PyLogAnalyser

    A Python multiplatform tool to filter, colorise and analyse logs

    PyLogAnalyzer is a tool that receives an input log in black and white, a configuration INI file, which contains the list of rules to process the input, and an output file where to save the results. These rules permit to detect an input line according to a regular expression (regex) or line number range, filter it, pass it, colorise in foreground and background, columnise the groups of the regex and enable or disable the rule. The final goal of this tool is to ameliorate reading long and difficult b/w logs, speed up the analysis and enhance day to day wearying activities. ...
    Downloads: 0 This Week
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  • 25
    iTag

    iTag

    Tag images using various categories and modifiers

    iTag has been designed for researchers that rely on photographic census techniques of animals that are hard to detect via image recognition algorithms and was originally developed for counting Grey Seals in the German wadden sea during March 2013. It has since then been further expanded and has now reached beta status. iTag allows Users to define up to 9 different categories and name them accordingly. In addition, 4 modifiers are available to further increase the options during a tagging session. ...
    Downloads: 0 This Week
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