Structural variant and indel caller for mapped sequencing data

STR genotyping with WGS and Amplicon/Target sequencing data

The Picontigotron is a small project to illustrate genome assembly on a Raspberry Pi

Structural variant toolkit for VCFs

Small game for point-neuron simulation

Comprehensive tutorial for differential methylation analysis, differential variability analysis and integrative analysis

R package for the analysis of massive SNP arrays.

Identify long STRs, VNTRs, satellite DNA and other low-complexity regions in a genome

A tool to genotype MUC1 coding VNTR in ADTKD

Highly Open Workflow for Annotation & Ranking toward genomic variant Discovery

Discovering known and novel miRNAs from small RNA sequencing data

A Toolset for Chromosome X-Wide Association Studies

An ultra-fast all-in-one FASTQ preprocessor (QC/adapters/trimming/filtering/splitting/merging...)

Guide pour l'analyse de données d'enquêtes avec R

Documentation on new GWAS Summary Statistics Standard

Modelling human health trajectories using generative transformers

Color palettes for gnuplot

Multi-sample somatic variant caller

GWAS Tutorial for Beginners

PolyFun (POLYgenic FUNctionally-informed fine-mapping)

A short tandem repeat (STR) genotyping and analysis toolkit for long reads

Work with trained factor models in Python

Pretty heatmaps

Summer School Multi-omics Data Analysis and Integration

CAncer Standards Long-read Evaluation

Multi-Omics Factor Analysis

R package to infer biological activities from omics data using a collection of methods.

A curated collection of Nextflow implementation patterns

A collection of resources to filter 'bad' probes from the Illumina 450k and EPIC methylation arrays