psytky03's Stars
chrisgrieser/alfred-bibtex-citation-picker
Picker for markdown-based citations and lightweight reference manager for BibTeX libraries.
ENCODE-DCC/caper
Cromwell/WDL wrapper for Python
kevboh/longform
A plugin for Obsidian that helps you write and edit novels, screenplays, and other long projects.
silentdot/zotero-markdown-translator
A simple Zotero translator that creates a Markdown Link when exporting
karkman/crAssphage_project
Source code for the crAssphage project
TCLamnidis/AdmixturePlotter
An R script to generate plots for ADMIXTURE runs, for multiple K values.
ScienceOlbrich/Admixture-Visualization
Some functions to facilitate plotting the output of PLINK in R.
Tom-Jenkins/admixture_pie_chart_map_tutorial
Tutorial for visualising admixture on a map
zhenyisong/zhen.lab
the scientific reproducible research
MareesAT/GWA_tutorial
A comprehensive tutorial about GWAS and PRS
DarkEyes/ipADMIXTURE
A data clustering package based on admixture ratios (Q matrix) of population structure analysis.
suhrig/arriba
Fast and accurate gene fusion detection from RNA-Seq data
opain/TWAS-GSEA
R script that performs gene-set or gene property analysis using TWAS results.
retorquere/zotero-better-bibtex
Make Zotero effective for us LaTeX holdouts
d2l-ai/d2l-en
Interactive deep learning book with multi-framework code, math, and discussions. Adopted at 500 universities from 70 countries including Stanford, MIT, Harvard, and Cambridge.
royfrancis/pophelper
An R package to analyse and visualise admixture proportions from STRUCTURE, fastSTRUCTURE, TESS, ADMIXTURE etc.
cggh/scikit-allel
A Python package for exploring and analysing genetic variation data
evotools/hapbin
Efficient program for calculating Extended Haplotype Homozygosity (EHH) and Integrated Haplotype Score (iHS)
brentp/poverlap
significance testing over interval overlaps
szpiech/selscan
Haplotype based scans for selection
bulik/ldsc
LD Score Regression (LDSC)
samtools/bcftools
This is the official development repository for BCFtools. See installation instructions and other documentation here http://samtools.github.io/bcftools/howtos/install.html
bioinf-jku/panelcn.mops
CNV detection tool for targeted NGS panel data
bcbio/bcbio-nextgen
Validated, scalable, community developed variant calling, RNA-seq and small RNA analysis
JoniColeman/gwas_scripts
Codebook from my GWAS cookbook
genomicsclass/labs
Rmd source files for the HarvardX series PH525x
joepickrell/1000-genomes-genetic-maps
Genetic maps interpolated to sites in the 1000 Genomes project
VertebrateResequencing/vr-codebase
The overall codebase developed and used by the Vertebrate Resequencing group at the Sanger Institute
blaze/blaze
NumPy and Pandas interface to Big Data
macarthur-lab/gene_lists
List of gene lists for genomic analyses.