713 Open source projects that are alternatives of or similar to Rasusa

goleft is a collection of bioinformatics tools distributed under MIT license in a single static binary

Fast & accurate alignment of barcoded short-reads

Data intensive science for everyone.

Python and C++ code for reading and writing genomics data.

A Python package for fast operations on 1-dimensional genomic signal tracks

Efficient variant-call data storage and retrieval library using the TileDB storage library.

Scalable genomic data analysis.

Configure linters and coverage tools to ignore Play's generated source files.

(No maintenance) Detect gene fusion directly from raw fastq files

A cross-platform and ultrafast toolkit for FASTA/Q file manipulation in Golang

🌊 A free REST API for random Kanye West quotes (Kanye as a Service)

Rust task runner and build tool.

Simultaneous detection of SNPs and Indels using a 16-genotype probabilistic model

Robust, flexible and resource-efficient pipelines using Go and the commandline

Single-Cell Analysis in Python. Scales to >1M cells.

A Gradle Plugin Providing Full Support for Go

Converts Cyrillic characters in post, page and term slugs to Latin characters. Useful for creating human-readable URLs.

The world's easiest, most powerful random function.

A collection of publications on comparison of high-throughput sequencing technologies.

In-memory nucleotide sequence k-mer counting, filtering, graph traversal and more

example for golang project using github actions

Actionable code coverage - detects untested code blocks in recent changes

some qml snippet.

JAMP - Just Another Metabarcoding Pipeline

Basically a script thrift shop

Random for modern C++ with convenient API

DEPRECIATED! Please use nf-core/tools instead

Javascript full-stack framework for Big Data visualisation and analysis

Data and analysis for the Splatter paper

Code coverage for Haxe

A robust model for quantitative comparison of ChIP-Seq data sets.

memory efficient, fast & precise taxnomomic classification system for metagenomic read mapping

Code coverage for Xcode projects (Objective-C only)

A versatile pairwise aligner for genomic and spliced nucleotide sequences

Toolkit for processing sequences in FASTA/Q formats

A wrapper for the EnsEMBL REST API

Aggregate results from bioinformatics analyses across many samples into a single report.

A full spaCy pipeline and models for scientific/biomedical documents.

A plotly.js React component from Plotly 📈

一个动态权重的随机算法

Scientific workflow engine designed for simplicity & scalability. Trivially transition between one off use cases to massive scale production environments

Seven Bridges API Client, CWL Schema, Meta Schema, and SDK Helper in R

Chance - Random generator helper for JavaScript

🎲 An open source app to choose randomly between numbers, answers, options and so on.

Express starter kit with ES2017+ support, testing, linting, and code coverage

Automatic random password generator class for PHP

Unix, R and python tools for genomics and data science

A cross-platform, efficient and practical CSV/TSV toolkit in Golang

UNCURL is a tool for single cell RNA-seq data analysis.

List of Computer Science courses with video lectures.

(formerly eelpond) an automated RNA-Seq workflow system

C library for high-throughput sequencing data formats

Estimate metagenomic coverage and sequence diversity

Code coverage tool for compiled programs, Python and Bash which uses debugging information to collect and report data without special compilation options

highly-efficient & lightweight mutation signature matrix aggregation

课题组每周研讨会

A lightweight immune repertoire browser

Secure, efficient, simple random session token generation

🐣 locally query the ncbi taxonomy