Differential RNA splicing analysis using rMAT¶
Summary¶
Differential splicing analysis using rMAT, one of the best tools.
Only works hg38.
Input¶
Example data dir: Projects/Siqi_data/RNAseq_data/Differential_Exon_Analysis/test
1. bam.tsv¶
3-col tsv, col1 is group1 bam files, seperated by commna. col2 is group2 bam files. col3 is comparison label.
GFP_pos_S2.markdup.uq.bam,GFP_pos_S3.markdup.uq.bam,GFP_pos_S8.markdup.uq.bam GFP_neg_S18.markdup.uq.bam,GFP_neg_S19.markdup.uq.bam,GFP_neg_S20.markdup.uq.bam GFP_pos_neg
H1_S1.markdup.uq.bam,H1_S3.markdup.uq.bam,H1_S5.markdup.uq.bam H2_S2.markdup.uq.bam,H2_S4.markdup.uq.bam,H2_S6.markdup.uq.bam H1_H2
SRR5890882_Fetal_d11.markdup.uq.bam,SRR5890883_Fetal_d11.markdup.uq.bam SRR5890878_Adult_d11.markdup.uq.bam,SRR5890879_Adult_d11.markdup.uq.bam FA11
SRR5890884_Fetal_d14.markdup.uq.bam,SRR5890885_Fetal_d14.markdup.uq.bam SRR5890880_Adult_d14.markdup.uq.bam,SRR5890881_Adult_d14.markdup.uq.bam FA14
Usage¶
make sure your readlength match --readLength 101.
hpcf_interactive
module load python/2.7.13
run_lsf.py -f bam.tsv --readLength 101 -p rMAT
Output¶
Results are stored in the $jid folder. Both paired-test (folder $COL3.RMATS.paired) and unpaired-test (folder $COL3.RMATS.unpaired) results are generated. If your data is unpaired, ignore it. Main result is *.MATS.JC.txt