Get upstream and downstream exon's starting site and ending site of an retained introns

Hi:

I have an output file from IRFinder to compare intron retention. It contains the chromosome, strand, intron start site, intron end site.

Now I would like to get the coordinates of the upstream/downstream exon starting and ending site. If there a way to get it done?

Thanks, Kai

rnaseq

• 1,686 views • link

updated 5.1 years ago by ATpoint

• written 5.1 years ago by Kai_Qi

If you have coordinates you could take a GTF file, extract only the exons, and then use something like bedtools closest to get the closest exons.

• 0 views • link

written 5.1 years ago by ATpoint

I have used the following ways to sort the exons:

library(GenomicFeatures)
txdb <- makeTxDbFromGFF("GRCm38_gene_125bp.gtf", format="gtf")
EX <- exons(txdb)
head(EX)
write.csv(as.data.frame(EX)[,-4], file="Exon_coordinates.csv", col.names=T)

Then I have convert the csv files into bed file and using my intron containing bedfile to finish the bedtools closest command:

head dynamic_IR_IRratio_cluster1_1.bed 
chr1    10059847    10064332    Cspp1/ENSMUSG00000056763/clean  .   +   1
chr1    121554138   121555215   Ddx18/ENSMUSG00000001674/clean  .   -   2
chr1    127803293   127803391   Ccnt2/ENSMUSG00000026349/known-exon .   +   3
chr1    130701851   130702230   Pfkfb2/ENSMUSG00000026409/clean .   -   4
chr1    134630753   134631236   Kdm5b/ENSMUSG00000042207/known-exon .   +   5
chr1    135405972   135406516   Ipo9/ENSMUSG00000041879/clean   .   -   6
chr1    135453288   135454044   Nav1/ENSMUSG00000009418/clean   .   -   7
chr1    136171306   136171587   Kif21b/ENSMUSG00000041642/clean .   +   8
chr1    170880226   170880572   Dusp12/ENSMUSG00000026659/known-exon    .   -   9
chr1    170880691   170880914   Dusp12/ENSMUSG00000026659/known-exon    .   -   10

The exons coordinates I used is:

head All_Exons_Coordinates_1.bed
chr1    3073253 3074322 3073253 .   +   2410
chr1    3102016 3102125 3102016 .   +   2411
chr1    3252757 3253236 3252757 .   +   2412
chr1    3466587 3466687 3466587 .   +   2413
chr1    3513405 3513553 3513405 .   +   2414
chr1    3531795 3532720 3531795 .   +   2415
chr1    3680155 3681788 3680155 .   +   2416
chr1    3752010 3754360 3752010 .   +   2417
chr1    4496551 4499378 4496551 .   +   2418
chr1    4497474 4497654 4497474 .   +   2419

Then I typed:

bedtools closest -a dynamic_IR_IRratio_cluster1_1.bed -b All_Exons_Coordinates_1.bed -s -D a > dynamic_IR_IRratio_cluster1_1_exon.bed
Error: Sorted input specified, but the file All_Exons_Coordinates_1.bed has the following out of order record

my aim is too get a file like this:

chr strand intron_start intron_end upstream_exon_start upstream_exon_end downstream_exon_start downstream_exon_end

Where is the problem of my code so that I got an error?

Thanks

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written 5.1 years ago by Kai_Qi

Where is the problem of my code so that I got an error?

I think the error is clear, your file is not properly sorted. Use either bedtools sort or sort -k1,1 -k2,2n to do that.

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written 5.1 years ago by ATpoint

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