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---
name: bio-epitranscriptomics-merip-preprocessing
description: Align and QC MeRIP-seq IP and input samples for m6A analysis. Use when preparing MeRIP-seq data for peak calling or differential methylation analysis.
tool_type: cli
primary_tool: STAR
---
# MeRIP-seq Preprocessing
## Alignment with STAR
```bash
# Build index (once)
STAR --runMode genomeGenerate \
--genomeDir star_index \
--genomeFastaFiles genome.fa \
--sjdbGTFfile genes.gtf
# Align IP and input samples
for sample in IP_rep1 IP_rep2 Input_rep1 Input_rep2; do
STAR --genomeDir star_index \
--readFilesIn ${sample}_R1.fastq.gz ${sample}_R2.fastq.gz \
--readFilesCommand zcat \
--outSAMtype BAM SortedByCoordinate \
--outFileNamePrefix ${sample}_
done
```
## QC Metrics
```bash
# Index BAMs
for bam in *Aligned.sortedByCoord.out.bam; do
samtools index $bam
done
# Check IP enrichment
# Good MeRIP: IP should have peaks, input should be uniform
samtools flagstat IP_rep1_Aligned.sortedByCoord.out.bam
```
## IP/Input Correlation
```python
import deeptools.plotCorrelation as pc
# Check replicate correlation
multiBamSummary bins \
-b IP_rep1.bam IP_rep2.bam Input_rep1.bam Input_rep2.bam \
-o results.npz
plotCorrelation -in results.npz \
--corMethod spearman \
-o correlation.png
```
## Related Skills
- **read-qc** - Raw read quality assessment
- **read-alignment** - General alignment concepts
- **m6a-peak-calling** - Next step after preprocessing