Per Unneberg
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Snakemake workflow to run variant calling and ARG inference
No description provided.
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Analyse, create and manipulate tree sequences.
Fast and flexible inference of the distribution of fitness effects (DFE), VCF-SFS parsing with ancestral allele and site-degeneracy annotation.
Partial reimplementation of bcftools for VCF Zarr
Cookiecutter for snakemake slurm profile
NBIS revealjs Quarto extension
Exploratory data analysis of d4 coverage files
NBIS course quarto template
This is the development home of the workflow management system Snakemake. For general information, see
Repository to host tool-specific module files for the Nextflow DSL2 community!
Analysis pipeline to detect germline or somatic variants (pre-processing, variant calling and annotation) from WGS / targeted sequencing
NBIS project administration utilities
GenomeLens GFF file parser
Convert bioinformatics file formats to Zarr
Manuscript and associated scripts for vcf-zarr publication
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A Snakemake storage plugin that reads and writes from a locally mounted filesystem using rsync.
The D4 Quantitative Data Format
Statistical genetics toolkit
Python utilities to work with d4 coverage files
Tree sequence workflow
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Infer the age of ancestral nodes in a tree sequence.
Utilities for evaluating inferred tree sequences
Whole genome tree sequence analyses
JupyterLite test for pgip