Posit Cheat Sheets - Can also be found at https://posit.co/resources/cheatsheets/.

RNA-seq aligner

Counting Reads for Intronic and Exonic Segments

Brain-related -omics data

Links to all data science, genomics, and other notes

A (continuously updated) collection of references to Hi-C data. Predominantly human/mouse Hi-C data, with replicates.

A list of scRNA-seq analysis tools

scATAC-seq data analysis tools and papers

A curated collection of currently available scATAC-seq datasets accessible through R, and exportable to other languages.

Github Pages template based upon HTML and Markdown for personal, portfolio-based websites.

Collections of library structure and sequence of popular single cell genomic methods

R package with commonly used functions by the Jaffe lab

10x Genomics Linked-Read Diploid De Novo Assembler

Codes for Schizophrenia CellType project

Scripts used for analysis of data in paper, 'Neuronal brain region-specific DNA methylation and chromatin accessibility are associated with neuropsychiatric disease heritability'.

Codes for Primate CellType project

WGBS/NOMe-seq Data Processing & Differential Methylation Analysis

Find causal cell-types underlying complex trait genetics

In this project we will build a web portal for our GoT data analysis and visualization system. The website will integrate all the apps created in projects B-D with the help of the integration team …

【编程随想】整理的《太子党关系网络》，专门揭露赵国的权贵

V-SVA: An R Shiny application for detecting and annotating hidden sources of variation in single cell RNA-seq data

手把手教你使用 EndNote X9/NoteExpress

Source code of FUMA GWAS web application

handle mysql in python