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泡面哥汤达人的前世今生,从默默无闻到人人喊打【截止到2019年12月9日】

161 37 Updated Nov 16, 2021

PAML is a package of programs for phylogenetic analyses of DNA or protein sequences using maximum likelihood. Please report only **technical issues** on this repository (e.g., compiling, programs a…

C 144 23 Updated Jan 24, 2025

BootStrap on Seurat (single cell object) to evaluate cluster stability.

4 Updated Jan 26, 2022

R package with collection of functions created and/or curated to aid in the visualization and analysis of single-cell data using R.

R 243 24 Updated Mar 6, 2025

An R package for learning complex single cell trajectory and expression trends

HTML 3 5 Updated Jul 31, 2021

Algorithm for the inference of cell types and lineage trees from single-cell RNA-seq data. This is a novel R package of the RaceID3 and StemID2 method including novel functionalities and performanc…

R 43 11 Updated Nov 25, 2024
R 20 9 Updated Mar 16, 2019

Pathway-based trajectory inference method for time-series scRNAseq data

R 25 6 Updated May 18, 2021

Gene set scoring for single-cell data

R 143 17 Updated Nov 1, 2024

Program to run the SOWH test (likelihood-based test used to compare tree topologies which are not specified a priori)

Perl 11 4 Updated May 3, 2024

Pilon is an automated genome assembly improvement and variant detection tool

Scala 351 60 Updated Apr 10, 2022

FALCON: experimental PacBio diploid assembler -- Out-of-date -- Please use a binary release: https://github.com/PacificBiosciences/FALCON_unzip/wiki/Binaries

Python 204 102 Updated Mar 4, 2022

R package for detecting doublets in single-cell RNA sequencing data

R 445 116 Updated Feb 3, 2025

Code for the empty droplet and cell detection project from the HCA Hackathon.

TeX 20 4 Updated Feb 26, 2019

Clone of the Bioconductor repository for the DropletUtils package.

R 57 28 Updated Dec 10, 2024

Computational correction of copy-number effect in CRISPR-Cas9 essentiality screens

R 27 15 Updated Mar 21, 2019
Python 64 31 Updated Aug 19, 2023

RNA-seq aligner

C 1,941 516 Updated Jun 28, 2024

Community-provided extensions to Seurat

R 322 136 Updated Nov 22, 2024
Jupyter Notebook 35 17 Updated Oct 25, 2018

Single RNA-seq data analysis with R (Finland, May, 2019)

HTML 220 106 Updated Aug 1, 2022

R script for processing scRNAseq data

R 1 Updated Dec 18, 2020

Fast, sensitive and accurate integration of single-cell data with Harmony

R 554 102 Updated Nov 11, 2024

A benchmark of batch-effect correction methods for single-cell RNA sequencing data

Jupyter Notebook 74 46 Updated Jan 24, 2022

The following code accompanies a manuscript combining single-cell RNA-sequencing and genotyping to analyze cellular hierarchies in acute myeloid leukemia (AML).

R 37 12 Updated Apr 8, 2020

r package for post-clustering curation of amplicon next generation sequencing data (metabarcoding)

Shell 63 17 Updated Dec 21, 2023

Multi-study integration of cellular trajectories

Python 19 3 Updated Jun 1, 2020

Software for clustering de novo assembled transcripts and counting overlapping reads

C++ 71 20 Updated Feb 11, 2022
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