Showing 18 open source projects for "disease"

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  • 1
    clusterProfiler

    clusterProfiler

    A universal enrichment tool for interpreting omics data

    ...It supports both over-representation analysis and gene set enrichment analysis, letting you work with unranked gene lists or ranked statistics from differential pipelines. The package connects to multiple knowledge bases—such as Gene Ontology, KEGG, Reactome, Disease Ontology, MeSH and others—through a consistent interface so you can query different biological lenses without rewriting code. It is designed for breadth, covering coding and non-coding features and thousands of organisms by leveraging continuously updated annotations. Results are returned in tidy, manipulation-friendly structures and pair naturally with rich visualization functions (via companion tooling) to summarize pathways, terms, and gene–set relationships.
    Downloads: 0 This Week
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  • 2
    illness index

    illness index

    illness_index A Computer Program of a Medical Textbook.

    ...The program also calculates a list of likely diseases, which the user can use the web to find out more about. The program has more than 600 diseases and 1000 findings. Brought to you by Kit Free Software 2024 Ltd. Keywords - disease, health, healthcare, illnesses, illnessindex, illness_index.
    Downloads: 0 This Week
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  • 3
    PANDORA

    PANDORA

    Revolutionizing Biomedical Research with Advanced Machine Learning

    PANDORA is a machine learning (ML) tool that can be used to integrate various data types, including clinical, transcriptome and microbiome data and find connections in large datasets. PANDORA can be easily installed using Docker, a pre-built version of the software can be pulled from DockerHub. In order to run a test instance of PANDORA, users will first need to prepare their local environment by downloading, installing, and configuring Docker. genular is a community behind SIMON an...
    Downloads: 2 This Week
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  • 4
    scArches

    scArches

    Reference mapping for single-cell genomics

    Single-cell architecture surgery (scArches) is a package for reference-based analysis of single-cell data. scArches allows your single-cell query data to be analyzed by integrating it into a reference atlas. By mapping your data into an integrated reference you can transfer cell-type annotation from reference to query, identify disease states by mapping to healthy atlas, and advanced applications such as imputing missing data modalities or spatial locations.
    Downloads: 0 This Week
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    covid19

    covid19

    Tokyo COVID-19 Task Force website

    New coronavirus infectious disease control site. In Tokyo, in order to centrally announce the infection status in Tokyo, we received reports of outbreaks not only in the jurisdiction of the Tokyo Health Center but also in the cities with health centers (Machida City, Hachioji City) and 23 wards, and aggregated these. In Tokyo, we have set seven monitoring items for the new coronavirus infection, with the two pillars of "infection status" and "medical care provision system" in Tokyo. ...
    Downloads: 0 This Week
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  • 6
    coronavirus

    coronavirus

    The coronavirus dataset

    ...The raw data is pulled and arranged by the Johns Hopkins University Center for Systems Science and Engineering, which is gathered from various leading sources including the World Health Organization, China CDC, US CDC, European Centre for Disease Prevention and Control, and Australia Government Department of Health.
    Downloads: 0 This Week
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  • 7
    HealthFusion

    HealthFusion

    AI Disease Detections System

    HealthFusion has identified a critical business problem, which is the lack of accessibility and timely detection of multiple diseases. The traditional approach of detecting diseases is time-consuming, expensive, and not accessible to everyone, especially in remote areas. This problem can lead to delayed diagnosis and treatment, which can have serious consequences for patients. The proposed solution, HealthFusion, is novel and practical as it offers a comprehensive solution to detect...
    Downloads: 0 This Week
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  • 8
    corona-cli

    corona-cli

    Track the Coronavirus disease (COVID-19) in the command line

    Track the Coronavirus disease (COVID-19) in the command line. Worldwide for all countries, for one country, and the US States. Fast response time (< 100ms).Get worldwide Coronavirus disease (COVID-19) reporting. Active daily reporting of your country's COVID-19 statistics. Get US States data for Coronavirus disease reports across the US. Data includes country, cases, deaths, recovered, active, critical, per million.
    Downloads: 0 This Week
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  • 9

    ICD 10 Disease Viewer

    Simplifies viewing of ICD 10 codes and descriptions by medical workers

    Helps medical personnel search and become familiar with ICD 10 disease codes and descriptions
    Downloads: 0 This Week
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  • 10
    The Disease Ontology has moved to Github. New project page: https://github.com/DiseaseOntology Disease Ontology is a stuctured controlled vocabulary originally based upon and mapped to medical billing codes. The goal of this ontology is to create a comprehensive hierachical controlled vocabulary to represent subsumptive disease relationships.
    Downloads: 0 This Week
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  • 11
    Hetionet

    Hetionet

    Hetionet: an integrative network of disease

    Hetionet is a hetnet — network with multiple node and edge (relationship) types — which encodes biology. The hetnet was designed for Project Rephetio, which aims to systematically identify why drugs work and predict new therapies for drugs. The JSON and Neo4j formats contain node and edge properties, which are absent in the TSV and matrix formats, including licensing information. Therefore the recommended formats are JSON and Neo4j. Our hetio package in Python reads the JSON format, but it...
    Downloads: 0 This Week
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  • 12

    CVDdb

    Cerebrovascular Disease database

    Our integrated database schema is an add-on schema to Loris (http://loris.ca/, Das et al, 2011), and includes 3079 subjects and over 550 federated and searchable data items including imaging details, medical history and examination, stroke and laboratory details, which maps to large multi-centre stroke trials with imaging data from over 10,000 patients from 30 countries. Here we provide our current version of our schema, and data dictionary. The data itself is for internal access only during...
    Downloads: 0 This Week
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  • 13

    Random Bits Regression

    Random Bits Regression is a strong general predictor.

    ...The accuracy and robustness improvement of our method over existing method could bring huge benefits in some critical applications. For example, natural disaster prediction, stock price prediction, personal/population disease prediction. The fast-speed nature of our method not only allows big data analysis but also enables real-time recognition and predictions. The RBR framework also hints the mechanism of brain function and leads to a "wide learning" hypothesis. We believe that this method will make a great impact and enable many downstream applications.
    Downloads: 0 This Week
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  • 14

    ExAM-Exome_Analysis_And_Mining

    A whole exome sequencing analysis package and its graphical interface

    ...Here, we present an interactive and free analysis package, ExAM, dedicated to whole exome sequencing data analysis. It is accessible to non-computer scientists and provides a complete set of information, as well as decision support to prioritize candidate disease causing variants.
    Downloads: 0 This Week
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  • 15

    HomSI

    Homozygous Stretch Identifier from next-generation sequencing data

    ...This situation leads to the prevalence of recessive diseases among the members of these families. Homozygosity mapping is based on this observation and several recessive disease genes have been discovered with the help of this technique in consanguineous families. The researchers typically use SNP arrays to determine the homozygous regions and then search for the disease gene by sequencing the genes within this candidate disease loci. Recently, the advent of next generation sequencing enables the concurrent identification of homozygous regions and the detection of mutations relevant for diagnosis, using data from a single sequencing experiment. ...
    Downloads: 0 This Week
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  • 16
    Snp Viewer

    Snp Viewer

    A program for visualising Affymetrix SNP array data

    A program for visualising Affymetrix SNP array data for identification regions of homozygosity. Written to aid autozygosity mapping and aid the discovery of potential disease loci.
    Downloads: 0 This Week
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  • 17
    This disease-centric project contributes data integration and analysis tools from the Institute for Systems Biology (ISB). We offer this project to the research community to further our efforts in disease prediction and prevention.
    Downloads: 0 This Week
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  • 18
    Simple Disease Tracking for Daycares is a web application designed to assist and promote the provider's documentation of illnesses in a childcare setting.
    Downloads: 0 This Week
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