Banded Striped DNA Sequence Alignment

FAN-C: Framework for the ANalysis of C-like data

Segmented HAPlotype Estimation and Imputation Tool

Multiple sequence and structure alignment with top benchmark scores scalable to thousands of sequences. Generates replicate alignments, enabling assessment of downstream analyses such as trees and …

二代测序数据分析

♥ Essential Functions for DNA Manipulation

C++ DataFrame for statistical, Financial, and ML analysis -- in modern C++ using native types and contiguous memory storage

Use ChatGPT to summarize the arXiv papers. 全流程加速科研，利用chatgpt进行论文全文总结+专业翻译+润色+审稿+审稿回复

Python application to generate self-contained pages embedding IGV visualizations, with no dependency on original input files.

Open Source Web-based Laboratory Information Management System

Convert BAM alignment files into bedGraph and bigWig files

hight performance & useful tools for working with fastq and bam files

xHLA: Fast and accurate HLA typing from short read sequence data

liftover for python, made fast with cython

R package containing useful functions for mutational signature analysis

LeetCode in pure C

ASCAT R package

Workflow for Sequenza, cellularity and ploidy

Script to automatically create and run IGV snapshot batchscripts

Scientific and statistical computing with Rust.

minimizer-space de Bruijn graphs (mdBG) for whole genome assembly

This library provides implementations of many algorithms and data structures that are useful for bioinformatics. All provided implementations are rigorously tested via continuous integration.

This library provides HTSlib bindings and a high level Rust API for reading and writing BAM files.

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