Skip to content
View famosab's full-sized avatar

Highlights

  • Pro

Organizations

@ncbench

Block or report famosab

Block user

Prevent this user from interacting with your repositories and sending you notifications. Learn more about blocking users.

You must be logged in to block users.

Maximum 250 characters. Please don't include any personal information such as legal names or email addresses. Markdown supported. This note will be visible to only you.
Report abuse

Contact GitHub support about this user’s behavior. Learn more about reporting abuse.

Report abuse
Showing results
Python 3 6 Updated Aug 15, 2024

A tool to standardize VCF files from structural variant callers

Go 5 1 Updated Jul 15, 2025
Nextflow 12 9 Updated Dec 11, 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 3,429 174 Updated Aug 15, 2024

YAML template engine

Python 41 5 Updated Nov 27, 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 48 29 Updated Dec 3, 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 87 58 Updated Jan 7, 2026

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

Python 34 3 Updated Dec 19, 2025

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

Python 1,023 355 Updated Aug 24, 2024
Common Workflow Language 9 3 Updated Mar 26, 2024
HTML 29 6 Updated Oct 16, 2024

cython + htslib == fast VCF and BCF processing

Cython 423 75 Updated Oct 13, 2025

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

C++ 665 226 Updated Oct 31, 2025

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

Nextflow 1 2 Updated Dec 29, 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 32 Updated Nov 20, 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 29 Updated Jun 22, 2022

NGSNGS: Next generation simulator for next generation sequencing data

C++ 56 7 Updated Nov 27, 2024

A terminal spreadsheet multitool for discovering and arranging data

Python 8,721 320 Updated Jan 6, 2026

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 8 2 Updated Dec 1, 2025

Virtual whiteboard for sketching hand-drawn like diagrams

TypeScript 113,911 12,055 Updated Jan 7, 2026

⚡ Dynamically generated stats for your github readmes

JavaScript 77,828 29,074 Updated Jan 5, 2026
Next