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@guangxi Medical University
- Nanning,china
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05:56
(UTC +08:00)
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Starred repositories
Machine learning-based integration model with elegant performance
深度学习500问,以问答形式对常用的概率知识、线性代数、机器学习、深度学习、计算机视觉等热点问题进行阐述,以帮助自己及有需要的读者。 全书分为18个章节,50余万字。由于水平有限,书中不妥之处恳请广大读者批评指正。 未完待续............ 如有意合作,联系[email protected] 版权所有,违权必究 Tan 2018.06
Contains code to analyse the data from the paper: Immune profiling-based targeting of pathogenic T cells with ustekinumab in ANCA-associated glomerulonephritis
PRnet is a flexible and scalable perturbation-conditioned generative model predicting transcriptional responses to unseen complex perturbations at bulk and single-cell levels.
Cellular dynamics across aged human brains uncover a multicellular cascade leading to Alzheimer’s disease
Bioconductor workshop: Analysis of single-cell RNA-seq data with R and Bioconductor
Accompanying code for the tutorial: Annotating single cell transcriptomic maps using automated and manual methods
Data files and code for analysis of single-cell ccRCC data for the manuscript "Tumor-Specific Cell Populations in Clear Cell Renal Carcinoma Associated with Clinical Outcome Identified Using Single…
Code and annotations for the Tabula Muris single-cell transcriptomic dataset.
A python library for multi omics included bulk, single cell and spatial RNA-seq analysis.
omics data analysis using clusterProfiler ;)
Scripts for the Reay et al. GWAS of circulating retinol
Stata package for two-sample Mendelian randomization analyses using summary data
An extension for VS Code that visualizes data during debugging.
A complete guide for analyzing bulk RNA-seq data. Go from raw FASTQ files to mapping reads using STAR and differential gene expression analysis using DESeq2, using example data from Guo et al. 2019.
GENE-SWitCH project RNA-Seq analysis pipeline
A nextflow pipeline which integrates multiple omic data streams and performs coordinated analysis
Analysis pipeline to detect germline or somatic variants (pre-processing, variant calling and annotation) from WGS / targeted sequencing
QC and filtering of genome skims, followed by organelle assembly and/or genome analysis
Interactively analyze single cell genomic data
UniverSC: a flexible cross-platform single-cell data processing pipeline