DeepEventMine: End-to-end Neural Nested Event Extraction from Biomedical Texts
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Skin_Lesion_Detection_Deep_Learningby adriaromero
Python 39 Version:Current License: No License (No License)
Skin lesion detection from dermoscopic images using Convolutional Neural Networks
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Backend server for Genome Nexus
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Decrypting somatic mutation patterns to reveal the evolution of cancer
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Homebridge plugin for Awair
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SigProfilerPlotting provides a standard tool for displaying all types of mutational signatures as well as all types of mutational patterns in cancer genomes. The tool seamlessly integrates with other SigProfiler tools.
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Deep-Learning for Tidemark Segmentation in Human Osteochondral Tissues Imaged with Micro-computed Tomography
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Physical validation of molecular simulations
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Burden testing against public controls
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Medkey Hospital Information System main repository: Practice Management for Practicioners & Hospitals, EHR, Patient Engagement
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Snakemake-based workflow for detecting structural variants in WGS data
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Decentralized distributed database of genomic and clinical data.
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Recombination Landscape Estimation using Recurrent Neural Networks
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Interpretation of proteomics identification results
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Molecular Generation for Desired Transcriptome Changes with Adversarial Autoencoders
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(Incubation) Streams Healthcare Analytics Platform - To enable and inspire the next generation healthcare solutions
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Patient registration and outpatient diagnosis system to be used with OpenMRS
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A webpack plugin that wraps your bundle in a System.register
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Cloud-based single-cell copy-number variation analysis tool
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HGTector2: Genome-wide prediction of horizontal gene transfer based on distribution of sequence homology patterns.
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CADD scripts release for offline scoring. For more information about CADD, please visit our website
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Task-based gene regulatory network inference using single-cell or bulk gene expression data conditioned on a prior network.
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A+ forms. Would use again
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Open-source repository containing examples and documentation for the Cognizant XPRIZE Pandemic Response Challenge
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📦 Biip interprets the data in barcodes.
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a python module for generating protein contact maps and distance maps
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GORpipe is a tool based on a genomic ordered relational architecture and allows analysis of large sets of genomic and phenotypic tabular data using declarative query language, in a parallel execution engine.
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:hibiscus: lightweight transcriptome assembly for short reads and nanopore reads
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Biomedical Visualization and Analysis Framework
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dcHiC: Differential compartment analysis for Hi-C datasets
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GeneValidator: Identify problems with predicted genes
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Htmlwidgets binding R commands to the BioCircos.js library
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Clinical interpretation of somatic mutations in cancer
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TGS scaffolding
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Deconvolving tumor purity and ploidy by integrating copy number alterations and loss of heterozygosity
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NGSEP is an integrated framework for analysis of high throughput sequencing (HTS) reads. The main functionality of NGSEP is the variants detector, which allows to make integrated discovery and genotyping of Single Nucleotide Variants (SNVs), insertions, deletions, and genomic regions with copy number variation (CNVs).
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A database of paths that represent the mechanism of action from a drug to a disease in an indication.
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Eyes on your (genomic) data
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Medical device simulator for training healthcare professionals.
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Robust 3D Neuron Tracing / General 3D tree structure extraction in Python for 3D images powered by the Rivulet2 algorithm. Pain-free Install & use in 5 mins.
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Python 32 Version:Current License: Permissive (Apache-2.0)
Kaggle 2018 @ Human Protein Atlas Image Classification
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covid-19-image-repositoryby ml-workgroup
Python 32 Version:Current License: Proprietary (Proprietary)
Anonymized dataset of COVID-19 cases with a focus on radiological imaging. This includes images (x-ray / ct) with extensive metadata, such as admission-, ICU-, laboratory-, and patient master-data.
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Kidney Tumor Segmentation Challenge 2019: MIScnn - 3D Residual U-Net
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A python parser to simplify and build the VCF (Variant Call Format).
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A Python implementation of divisive and hierarchical clustering algorithms. The algorithms were tested on the Human Gene DNA Sequence dataset and dendrograms were plotted.
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An Artificial Neural Network-based discriminator for validating clinically significant genomic variants
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Powerful mechanism to sort arrays or array of objects by one or more properties. You can also specify a custom comparer function.
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Custom extension script for whistle
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The Genome U-Plot is a JavaScript tool to visualize chromosomal abnormalities in the Human Genome using a U-shape layout.
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HiGHmed Data Sharing Framework
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DeepEventMineby aistairc
DeepEventMine: End-to-end Neural Nested Event Extraction from Biomedical Texts
Python 39Updated: 3 y ago License: Permissive (Apache-2.0)
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Skin_Lesion_Detection_Deep_Learningby adriaromero
Skin lesion detection from dermoscopic images using Convolutional Neural Networks
Python 39Updated: 4 y ago License: No License (No License)
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genome-nexusby genome-nexus
Backend server for Genome Nexus
Java 39Updated: 2 y ago License: Permissive (MIT)
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treeomicsby reiterlab
Decrypting somatic mutation patterns to reveal the evolution of cancer
Python 39Updated: 4 y ago License: Strong Copyleft (GPL-3.0)
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homebridge-awairby deanlyoung
Homebridge plugin for Awair
JavaScript 39Updated: 4 y ago License: Permissive (MIT)
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SigProfilerPlottingby AlexandrovLab
SigProfilerPlotting provides a standard tool for displaying all types of mutational signatures as well as all types of mutational patterns in cancer genomes. The tool seamlessly integrates with other SigProfiler tools.
Python 38Updated: 2 y ago License: Permissive (BSD-2-Clause)
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mCTSegmentationby MIPT-Oulu
Deep-Learning for Tidemark Segmentation in Human Osteochondral Tissues Imaged with Micro-computed Tomography
Python 38Updated: 4 y ago License: Permissive (MIT)
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physical_validationby shirtsgroup
Physical validation of molecular simulations
Python 38Updated: 2 y ago License: Permissive (MIT)
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TRAPDby mhguo1
Burden testing against public controls
Python 38Updated: 2 y ago License: Permissive (MIT)
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medkeyby medkey-org
Medkey Hospital Information System main repository: Practice Management for Practicioners & Hospitals, EHR, Patient Engagement
PHP 38Updated: 3 y ago License: Strong Copyleft (GPL-3.0)
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sv-callersby GooglingTheCancerGenome
Snakemake-based workflow for detecting structural variants in WGS data
Python 37Updated: 3 y ago License: Permissive (Apache-2.0)
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cgtdby cancergenetrust
Decentralized distributed database of genomic and clinical data.
Python 37Updated: 5 y ago License: Permissive (Apache-2.0)
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ReLERNNby kr-colab
Recombination Landscape Estimation using Recurrent Neural Networks
Python 37Updated: 2 y ago License: Permissive (MIT)
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peptide-shakerby compomics
Interpretation of proteomics identification results
Java 37Updated: 2 y ago License: No License (No License)
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BiAAEby insilicomedicine
Molecular Generation for Desired Transcriptome Changes with Adversarial Autoencoders
Python 36Updated: 4 y ago License: Permissive (MIT)
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streamsx.healthby IBMStreams
(Incubation) Streams Healthcare Analytics Platform - To enable and inspire the next generation healthcare solutions
Java 36Updated: 4 y ago License: Permissive (Apache-2.0)
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matemeby baobab
Patient registration and outpatient diagnosis system to be used with OpenMRS
Ruby 36Updated: 5 y ago License: No License (No License)
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webpack-system-registerby CanopyTax
A webpack plugin that wraps your bundle in a System.register
JavaScript 36Updated: 4 y ago License: Permissive (Apache-2.0)
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ginkgoby robertaboukhalil
Cloud-based single-cell copy-number variation analysis tool
PHP 36Updated: 4 y ago License: Permissive (BSD-2-Clause)
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HGTectorby DittmarLab
HGTector2: Genome-wide prediction of horizontal gene transfer based on distribution of sequence homology patterns.
Python 35Updated: 4 y ago License: Permissive (BSD-3-Clause)
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CADD-scriptsby kircherlab
CADD scripts release for offline scoring. For more information about CADD, please visit our website
Python 35Updated: 4 y ago License: Proprietary (Proprietary)
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inferelatorby flatironinstitute
Task-based gene regulatory network inference using single-cell or bulk gene expression data conditioned on a prior network.
Python 35Updated: 2 y ago License: Permissive (BSD-2-Clause)
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a-plus-formsby MadRabbit
A+ forms. Would use again
JavaScript 35Updated: 4 y ago License: No License (No License)
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covid-xprizeby leaf-ai
Open-source repository containing examples and documentation for the Cognizant XPRIZE Pandemic Response Challenge
Python 35Updated: 4 y ago License: Proprietary (Proprietary)
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biipby jodal
📦 Biip interprets the data in barcodes.
Python 34Updated: 2 y ago License: Permissive (Apache-2.0)
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pconpyby kianho
a python module for generating protein contact maps and distance maps
Python 34Updated: 4 y ago License: Proprietary (Proprietary)
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gorby gorpipe
GORpipe is a tool based on a genomic ordered relational architecture and allows analysis of large sets of genomic and phenotypic tabular data using declarative query language, in a parallel execution engine.
Java 34Updated: 2 y ago License: Strong Copyleft (AGPL-3.0)
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RNA-Bloomby bcgsc
:hibiscus: lightweight transcriptome assembly for short reads and nanopore reads
Java 34Updated: 4 y ago License: Proprietary (Proprietary)
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Eidolonby ericspod
Biomedical Visualization and Analysis Framework
Python 34Updated: 2 y ago License: Strong Copyleft (GPL-3.0)
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dcHiCby ay-lab
dcHiC: Differential compartment analysis for Hi-C datasets
R 34Updated: 2 y ago License: Permissive (MIT)
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genevalidatorby wurmlab
GeneValidator: Identify problems with predicted genes
Ruby 34Updated: 4 y ago License: Strong Copyleft (AGPL-3.0)
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BioCircos.Rby lvulliard
Htmlwidgets binding R commands to the BioCircos.js library
JavaScript 34Updated: 3 y ago License: Strong Copyleft (GPL-2.0)
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CancerVarby WGLab
Clinical interpretation of somatic mutations in cancer
Python 34Updated: 2 y ago License: No License (No License)
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PyLOHby uci-cbcl
Deconvolving tumor purity and ploidy by integrating copy number alterations and loss of heterozygosity
Python 33Updated: 4 y ago License: Strong Copyleft (GPL-2.0)
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NGSEPcoreby NGSEP
NGSEP is an integrated framework for analysis of high throughput sequencing (HTS) reads. The main functionality of NGSEP is the variants detector, which allows to make integrated discovery and genotyping of Single Nucleotide Variants (SNVs), insertions, deletions, and genomic regions with copy number variation (CNVs).
Java 33Updated: 2 y ago License: Strong Copyleft (GPL-3.0)
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DrugMechDBby SuLab
A database of paths that represent the mechanism of action from a drug to a disease in an indication.
Jupyter Notebook 33Updated: 1 y ago License: Permissive (CC0-1.0)
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panoptesby cggh
Eyes on your (genomic) data
JavaScript 33Updated: 3 y ago License: Proprietary (Proprietary)
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infirmary-integratedby tanjera
Medical device simulator for training healthcare professionals.
C# 33Updated: 2 y ago License: Proprietary (Proprietary)
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rivuletpyby RivuletStudio
Robust 3D Neuron Tracing / General 3D tree structure extraction in Python for 3D images powered by the Rivulet2 algorithm. Pain-free Install & use in 5 mins.
Python 32Updated: 4 y ago License: Permissive (BSD-3-Clause)
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kaggle-human-protein-atlas-image-classificationby ildoonet
Kaggle 2018 @ Human Protein Atlas Image Classification
Python 32Updated: 4 y ago License: Permissive (Apache-2.0)
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c
covid-19-image-repositoryby ml-workgroup
Anonymized dataset of COVID-19 cases with a focus on radiological imaging. This includes images (x-ray / ct) with extensive metadata, such as admission-, ICU-, laboratory-, and patient master-data.
Python 32Updated: 3 y ago License: Proprietary (Proprietary)
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kits19.MIScnnby muellerdo
Kidney Tumor Segmentation Challenge 2019: MIScnn - 3D Residual U-Net
Python 32Updated: 2 y ago License: Strong Copyleft (GPL-3.0)
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VCF-Simplifyby everestial
A python parser to simplify and build the VCF (Variant Call Format).
Python 32Updated: 4 y ago License: Permissive (MIT)
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hierarchical-clusteringby shubhamjha97
A Python implementation of divisive and hierarchical clustering algorithms. The algorithms were tested on the Human Gene DNA Sequence dataset and dendrograms were plotted.
Python 32Updated: 4 y ago License: No License (No License)
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Skyhawkby aquaskyline
An Artificial Neural Network-based discriminator for validating clinically significant genomic variants
Python 32Updated: 4 y ago License: Proprietary (Proprietary)
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array-sort-byby jherax
Powerful mechanism to sort arrays or array of objects by one or more properties. You can also specify a custom comparer function.
JavaScript 32Updated: 4 y ago License: Permissive (ISC)
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whistle.scriptby whistle-plugins
Custom extension script for whistle
JavaScript 32Updated: 4 y ago License: Permissive (MIT)
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GenomeUPlotby gaitat
The Genome U-Plot is a JavaScript tool to visualize chromosomal abnormalities in the Human Genome using a U-shape layout.
JavaScript 32Updated: 3 y ago License: No License (No License)
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highmed-dsfby highmed
HiGHmed Data Sharing Framework
Java 32Updated: 2 y ago License: Permissive (Apache-2.0)
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