Build BSgenome by youself in OS environment

With the package sangerseqR, we can easily read and manipulate abi files

ow to heck the ab1 data with R or Python

Delete low maped reads from count or expression matrix

R package for Bioinformatics; made by Doc. Yu

WGCNA in action.

WGCNA Tutorial 2

WGCNA Tutorial 1

R library for fasta sequences handling.

Codes for hot to running EdgeR to call differential Expression Genes from RSEM result. (More details you can find in Trinity wiki)