RNAseq
I passed my defense on Tuesday, and now I am a PhD! what a long process, it took me six years. I’ve been enjoying the PhD experience though.
I was working on a human RNA-seq data set, and I already got the count matrix by HTSeq.\ see my previous post here RNA-seq analysis samtools sort and…
I am following the RNA-seq nature protocol from Simon Anders. See my previous post here:Two nature protocols for RNA-seq analysis
It took me 45 hrs to map a 24G single-end RNA-seq data to human hg19 with the gtf file from GENECODE!
Usually we detect mutations by DNA-sequencing or whole exome sequencing, GATK is the commonly used pipeline for this purpose.
A very nice article comparing FPKMs and raw counts in RNA-seq data analysis
Align RNA-seq with Tophat
One is from Simon Anders, his group wrote the DESeq
Thank you Simon and your team!
It is a python package for visualizing the RNA-seq data.