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Showing results
Python 3 5 Updated Aug 15, 2024

A tool to standardize VCF files from structural variant callers

Go 4 1 Updated Jul 15, 2025

Analysis pipeline for the functional annotation and translation of somatic SNVs/InDels and copy number abberations for precision cancer medicine using PCGR

Nextflow 10 9 Updated Oct 28, 2025

Generate input samplesheet file compatible with nf-core pipelines from FASTQ files in a given AWS S3 bucket or a local directory

Shell 1 Updated Sep 5, 2025

A simple app to get songs from YouTube in mp3 format with artist name, album name etc from sources like iTunes, Spotify, LastFM, Deezer, Gaana etc.

Python 3,401 171 Updated Aug 15, 2024

YAML template engine

Python 38 5 Updated Aug 25, 2025

v2.x of the microassembly based somatic variant caller

C++ 23 4 Updated Jul 16, 2025

Functionality for working with pipeline and sample sheet schema files in Nextflow pipelines

Groovy 45 28 Updated Oct 27, 2025

Fast retrieval of metadata and fastq files with ffq and aria2

Python 7 Updated Apr 4, 2025

Differential abundance analysis for feature/ observation matrices from platforms such as RNA-seq

Nextflow 84 57 Updated Oct 27, 2025

A pipeline that accurately simulates high quality publicly cancer genomes (VCFs, CNAs and SVs).

Python 30 2 Updated Sep 1, 2025

Validated, scalable, community developed variant calling, RNA-seq and small RNA analysis

Python 1,018 355 Updated Aug 24, 2024
Common Workflow Language 7 3 Updated Mar 26, 2024
HTML 29 6 Updated Oct 16, 2024

cython + htslib == fast VCF and BCF processing

Cython 415 75 Updated Oct 13, 2025

C++ library and cmdline tools for parsing and manipulating VCF files with python and zig bindings

C++ 660 225 Updated Oct 31, 2025

Nextflow pipeline to transform (g)VCF files to matrices for statistical analysis.

Nextflow 1 2 Updated Jul 14, 2025

A pipeline for the analysis of CRISPR edited data. It allows the evaluation of the quality of gene editing experiments using targeted next generation sequencing (NGS) data (`targeted`) as well as t…

Nextflow 53 33 Updated Oct 23, 2025

VarSim: A high-fidelity simulation validation framework for high-throughput genome sequencing with cancer applications

Java 90 31 Updated Oct 3, 2024

Simulation and variant calling in paired-end, targeted sequencing saturation mutagenesis data.

Python 8 1 Updated May 31, 2024

NGS read simulator to eliminate read nucleotide bias in sequence analysis.

Rust 6 Updated Mar 19, 2023

a novel next-generation sequencing simulator using position and genomic contexts based error profiles

C++ 13 7 Updated Dec 18, 2020

NEAT read simulation tools

Python 101 28 Updated Jun 22, 2022

NGSNGS: Next generation simulator for next generation sequencing data

C++ 54 6 Updated Nov 27, 2024

A terminal spreadsheet multitool for discovering and arranging data

Python 8,537 312 Updated Oct 9, 2025

A GitHub action to build an html preview from an RO Crate and publish to the gh-pages branch

Dockerfile 5 Updated May 15, 2023

Scripts for deploying nf-core pipelines and testing new Nextflow plugins against them.

Shell 1 Updated Jan 31, 2025

A Rust library for defining RO-Crates (https://www.researchobject.org/ro-crate/1.1/) for research data.

Rust 1 Updated Apr 5, 2025

Virtual whiteboard for sketching hand-drawn like diagrams

TypeScript 109,707 11,413 Updated Nov 4, 2025

⚡ Dynamically generated stats for your github readmes

JavaScript 76,800 26,734 Updated Nov 3, 2025
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