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gene_sets

Mendelian disorder gene sets for specific traits, created from mining OMIM for phentoype-specific clinical keywords

ggplot2_workshop

Material for "Drawing Anything with ggplot2" workshop

gnomad-browser

gnomad_methods

Hail helper functions for the gnomAD project and Translational Genomics Group

gnomad_qc

graphbio

GraphBio: a shiny web app to easily perform popular visualization analysis for omics data

hotspot3d

3D hotspot mutation proximity analysis tool

list

Local Identity and Shared Taxa

litemol

A library/plugin for handling 3D structural molecular data (not only) in the browser.

locnuclei

Prediction of subnuclear locations

lollipops

Lollipop-style mutation diagrams for annotating genetic variations.

machine-learning

Practical Full-Stack Machine Learning

mantis-ml-release

mantis-ml: Stochastic semi-supervised learning to prioritise genes from high throughput genomic screens

mapping

ChemoProteomic-Detected Amino Acids (CpDAAs) to missense deleteriousness predictions and ClinVar pathogenic mutations

mapresiduefeatures

mendelianrna-seq

miscastv1.0

mmtf-genomics

Methods for mapping genomic data onto 3D protein structure.

molart

MOLeculAR structure annoTator

multilableaderboard

This is a paper reading tracker app for multiple labs to compare their average reading

mutscore

myvariant.info

MyVariant.info: A BioThings API for human variant annotations

nightingale

Data visualisation web components for the life sciences.

numpy-100

100 numpy exercises (100% complete)

pathoscore

pathoscore evaluates variant pathogenicity tools and scores.

pdb2uniprot

Convert PDB residues to their Uniprot equivalents

pers

Pathogenic variant enriched regions tutorial, examples and additional files

plots

pythondatasciencehandbook

Python Data Science Handbook: full text in Jupyter Notebooks

r4ds

R for data science: a book