8000 lindayqlin (Linda Lin) / Starred · GitHub
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GCTA software

C++ 96 26 Updated Mar 17, 2025

Development for SAIGE and SAIGE-GENE(+)

C++ 76 27 Updated May 19, 2025

regenie is a C++ program for whole genome regression modelling of large genome-wide association studies.

C++ 215 60 Updated Jan 28, 2025
Python 12 Updated Mar 27, 2025
Jupyter Notebook 8 Updated May 17, 2025

GenomeStrip builds

q 2 Updated Nov 15, 2018

fast BAM/CRAM depth calculation for WGS, exome, or targeted sequencing

Nim 745 100 Updated Jan 17, 2025

Modin: Scale your Pandas workflows by changing a single line of code

Python 10,165 664 Updated May 23, 2025

R package for "sum of single effects" regression.

R 214 53 Updated May 13, 2025

Assembled Genomes Compressor

C++ 164 13 Updated Nov 25, 2024

A python package for fitting a wide variety of Mixture Models

Jupyter Notebook 6 2 Updated Aug 24, 2024

Implementation of the paper: 'Robust mixture modelling using the t distribution', D. Peel and G. J. McLachlan.

Python 30 8 Updated Dec 20, 2023

PGR-TK: Pangenome Research Tool Kit

Rust 99 13 Updated Apr 22, 2024

A versatile pairwise aligner for genomic and spliced nucleotide sequences

C 1,966 433 Updated May 18, 2025

flexible barcode and adapter removal

C++ 80 27 Updated Feb 10, 2023

Tool package to perform in-silico CRISPR analysis and assessment

Python 25 9 Updated May 3, 2024

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

C++ 646 223 Updated May 18, 2025

use WFA2 to scan for CRISPR guide targets

Rust 1 2 Updated May 2, 2025

displays multiple genomic sequences in the form of a tube map

JavaScript 195 27 Updated May 15, 2025

Variant Calling for the HPRC Release 2

Nextflow 10 Updated Apr 1, 2025

Symmetric DUST for finding low-complexity regions in DNA sequences

C 42 9 Updated Aug 29, 2023

Code repository for the T2T-Y paper

Python 24 3 Updated Jul 11, 2023

Pangenome-based genome inference

C++ 127 12 Updated Apr 15, 2025

Easy genomic regions for short-read variant calling

Gnuplot 13 Updated Feb 25, 2025

PLINK is a free, open-source whole genome association analysis toolset, designed to perform a range of basic, large-scale analyses in a computationally efficient manner. This is a comprehensive upd…

C 455 132 Updated May 22, 2025

Structural variant detection and association testing

C++ 107 25 Updated Feb 2, 2023

Structural variant and indel caller for mapped sequencing data

C++ 428 152 Updated Dec 21, 2022

A structural variation pipeline for short-read sequencing

Python 188 75 Updated May 22, 2025
1 Updated Feb 7, 2025

Evaluating genome assemblies

C 91 9 Updated Mar 9, 2025
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