https://tuixue.online/visa/ A Real-time Display of U.S. Visa Appointment Status Website 预约美帝签证各个签证处最早时间的爬虫

Detecting DNA methylation from PacBio CCS reads

Machine Learning with data from the Multiple Myeloma Research Foundation

An R-Package to Visualize the (Causal) Effect of a Continuous Variable on a Time-To-Event Outcome

Variance stabilizing transformation for Gamma Poisson distributed data

Experimental design framework for scRNAseq population studies (eQTL and DE)

Github repository for nanoSPLITS manuscript data and R scripts

Structural variation caller using third generation sequencing

Probabilistic model for inferring clonal population structure from deep NGS sequencing.

Color blindness friendly visualization of single-cell and bulk RNA-sequencing data

DeepSeek-V2: A Strong, Economical, and Efficient Mixture-of-Experts Language Model

R toolkit for inference, visualization and analysis of cell-cell communication from single-cell and spatially resolved transcriptomics

Repo for the R package coloc

A tool for semi-automatic cell type harmonization and integration

An end-to-end Single-Cell Pipeline designed to facilitate comprehensive analysis and exploration of single-cell data.

NeoFuse is a user-friendly pipeline for the prediction of fusion neoantigens from tumor RNA-seq data.

A software package for connecting cell level features in single cell RNA sequencing data with receptor ligand activity. Please be aware that an improved package, dominoSignal, is available.

Bayesian Segmentation of Spatial Transcriptomics Data

SigProfilerMatrixGenerator creates mutational matrices for all types of somatic mutations. It allows downsizing the generated mutations only to parts for the genome (e.g., exome or a custom BED fil…

SigProfilerExtractor allows de novo extraction of mutational signatures from data generated in a matrix format. The tool identifies the number of operative mutational signatures, their activities i…

Battenberg R package for subclonal copynumber estimation

Support code for NGS copy number algorithms. Takes a file of locations and a [cr|b]am file and generates a count of coverage of each allele [ACGT] at that location (given any filter settings)

inotify-tools is a C library and a set of command-line programs providing a simple interface to inotify.