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Megadesk ⭐ 643

Open-source IKEA Bekant controller board

Cikonss ⭐ 407

Schema Org Rdf ⭐ 180

Schema.org in RDF

D3stryr 3stripes ⭐ 153

Python 3 implementation of d3stryr-3stripes

VCF visualization interface

D3js Orgchart ⭐ 126

D3.js Organizational chart

Benchmarking Tools ⭐ 110

Repository for the GA4GH Benchmarking Team work developing standardized benchmarking methods for germline small variant calls

Angular Bootstrap Datetimepicker Directive ⭐ 69

A wrapper directive around the bootstrap-datetimepicker component.

Ocamlcheatsheet ⭐ 60

Reference of basic commands to get comfortable with OCaml.

Licensechecker ⭐ 48

Gradle plugin to check that all Open Source Libraries in a project have been attributed

Tailwindcss Rfs ⭐ 43

This is a Tailwind CSS plugin to generate utility classes for RFS

Usb Live Linux ⭐ 32

USB-Stick-Live-Softwareumgebung für Lernende und Lehrende jeden Alters: Schulstick, Unistick, Makerstick, Rentnerstick..

Bcbio_validations ⭐ 28

Validation runs using bcbio: germline, somatic, structural variant calling and RNA-seq analyses

A JavaScript library for creating websites, PWAs and hybrid apps.

Bilara Data ⭐ 24

Content for Bilara translation webapp.

Ngs Course.github.io ⭐ 23

Reachvarianteditor ⭐ 23

A tool for editing Halo: Reach game variants.

A small repo for storing the code for making the files and html for CCRs.

Genomeanalysismodule ⭐ 21

Welcome to the website and github repository for the Genome Analysis Module. This website will guide the learning experience for trainees in the UBC MSc Genetic Counselling Training Program, as they embark on a journey to learn about analyzing genomes.

Fsharpcheatsheet ⭐ 19

Reference sheet of the basics of F# ^_^

Contentful Commerce ⭐ 19

How to Build a Static Site Ecommerce with Jekyll, Contentful, and Commerce Layer

FInding REliable Variants without ArTifacts

Gpl History ⭐ 14

Online tracker for Pokemon GO

Spliceai Lookup ⭐ 13

web app for checking SpliceAI and Pangolin scores

Seave is a web platform that enables genetic variants to be easily filtered and annotated with in silico pathogenicity prediction scores and annotations from popular disease databases. Seave stores genomic variation of all types and sizes, and allows filtering for specific inheritance patterns, quality values, allele frequencies and gene lists. Seave is open source and deployable locally, or on a cloud computing provider, and works readily with gene panel, exome and whole genome data, scaling fr

Bannerbuilder ⭐ 12

NPM/Gulp based banner build setup that allows for easy setup and build of similar HTML banners by variation and size

Supports de cours de l'Ecole de Bioinformatique Aviesan - IFB - Inserm "Initiation au traitement des données de génomique obtenues par séquençage à haut débit"

Cruk Summer School 2017 ⭐ 11

Analysis of Cancer Genomes; 2017 edition

Doesnaughtcompute ⭐ 11

Code and example datasets for Does[0]Compute

JAVA framework for accurate SNV assessment

Pdx_exomeseq ⭐ 9

Pipeline analysis for whole exome sequencing of pancreatic cancer PDX models

Aaags_2018 ⭐ 9

Course Materials for AAAGs 2018 Workshop

JARVIS: a comprehensive deep learning framework to prioritise non-coding variants in whole genomes

Uniform Latin Keyboard Layouts - intuitive, nationalized, multiplatform, powerful, and basically 100% mutually compatible (also with Dvorak)

Node Metamap ⭐ 8

Package providing access to the MetaMap Web API for UMLS

Gentb Site ⭐ 8

The genTB project, the Django site, variant calling and prediciton pipeline, and mapping pipeline with hooks to two ravens

Utrannotator ⭐ 7

VEP Plugin to annotate high-impact five prime UTR variants

Denovolyzer ⭐ 7

An R package for statistical analyses of de novo genetic variants

CoV-Seq: COVID-19 Genomic Sequence Database and Visualization

Genetics Sumstat Data ⭐ 6

Workflows for processing summary statistics files for Open Targets Genetics

Rmahunter ⭐ 6

HTML5 puzzle game where you solve nonograms.

HTML/CSS framework for creating App Store-like user interfaces

Betterselectlist ⭐ 5

Better select lists for ASP.NET MVC

Variant_calling_in_cancer_genomes_seminar ⭐ 5

Variant Calling in Cancer Genomes

Wet Boew Ssi ⭐ 5

SSI variant of the Web Experience Toolkit (WET)

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