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Java 5 Updated Jul 17, 2023

A curated collection of Nextflow implementation patterns

Nextflow 361 73 Updated Nov 21, 2023

Turn an existing conda environment into a Singularity container

Python 80 15 Updated Dec 14, 2022

Lightweight lockfile for conda environments

Python 521 108 Updated Jun 5, 2025

Pairtree is a method for reconstructing cancer evolutionary history in individual patients, and analyzing intratumor genetic heterogeneity. Pairtree focuses on scaling to many more cancer samples a…

Python 37 10 Updated Apr 18, 2024

Mixed-effect model to test differences in cell type proportions from single-cell data, in R

R 105 8 Updated Jun 5, 2025

easy simd

Rust 355 26 Updated Feb 11, 2025

A grammar of graphics for comparative genomics

R 680 67 Updated Jan 31, 2025

Deepfakes Software For All

Python 54,072 13,410 Updated May 21, 2025

A free and open-source pedigree tool by PhenoTips®

JavaScript 49 25 Updated Jan 10, 2024

Robust detection of clinically relevant structural and copy number variation from whole genome sequencing data

Perl 69 8 Updated Sep 4, 2024

A package that makes Julia take advantage of cool terminal emulator features.

Julia 42 11 Updated Aug 20, 2021

Another Gtf/Gff Analysis Toolkit https://nbisweden.github.io/AGAT/

Perl 507 58 Updated Apr 15, 2025

RTG Tools: Utilities for accurate VCF comparison and manipulation

Java 318 52 Updated May 27, 2025

phasing and Allele Specific Expression from RNA-seq

Python 115 35 Updated Jul 14, 2024
Python 6 1 Updated Jan 12, 2022

QDNAseq bin annotation for hg38

R 15 5 Updated Apr 1, 2025

Somatic mutation calling on moderately deep WES data using GATK/MuTect

Python 2 Updated Jan 23, 2017

Genome Interval Arithmetic in R

R 91 25 Updated Apr 29, 2025

Clone trees for Cancer Evolution studies from bulk sequencing data.

R 5 2 Updated May 6, 2025

Log-normal-Poisson regression model from Hess et al. 2019

MATLAB 5 2 Updated Sep 20, 2019

Chromosome visualization for the web

JavaScript 301 74 Updated May 20, 2025

Structural variant toolkit for VCFs

Python 358 51 Updated May 6, 2025

HATCHet (Holistic Allele-specific Tumor Copy-number Heterogeneity) is an algorithm that infers allele and clone-specific CNAs and WGDs jointly across multiple tumor samples from the same patient, a…

Roff 69 32 Updated Feb 26, 2025

Single-Cell Genotyping Tool

Rust 206 26 Updated Oct 2, 2023

An R package to time somatic mutations

R 61 22 Updated Dec 12, 2020

dN/dS methods to quantify selection in cancer and somatic evolution

HTML 222 49 Updated May 15, 2025

R data package for annotating/converting Gene IDs

R 163 33 Updated Feb 21, 2023

Fork of the Polysolver project

Perl 31 18 Updated Nov 21, 2019

C++ Implementation of a standard bloom filter, using MurmurHash (v2)

C++ 1 1 Updated Feb 3, 2013
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