RNA-seq
TODO Summary
How to analyze RNA-seq data
Understand what the data looks like
1. Quality control
Larger error means the data quality is poor
Identify failed sequencing experiments
Filter out those low quality reads
Trim off those low quality fragments
Reduce sequencing error caused noise as much as possible for downstream analysis
2. Mapping to reference database
3. Quantify gene expression
4. Identify differentially expressed genes
TSS Assays
GRO-cap
PRO-cap
CoPRO
Start-seq
CAGE
RAMPAGE
NET-CAGE
csRNA-seq
STRIPE-seq