Hello All,
I have Differentially expressed gene list from RNA-seq data, I have compared Drug treated v/s Untreated And I have got differentially expressed gene list which I have pasted in the following table.
My question is, when I use R/Bioconductor package "cummeRbund" to inspect the number of genes and transcript that are differentially expressed b/w two sample, I have loaded the results of cuffdiff's analysis , which reports the number of differentially expressed genes. The differentially expressed genes is not annotated (XLOC_000007), is their any way to annotate gene_id with actual gene names?
Control vs Treated Data
Differentially expressed Genes
gene_id sample_1 sample_2 status value_1 value_2 log2_fold_change test_stat p_value q_value significant
XLOC_000007 treated control OK 2.35097 1.35961 -0.790057 -3.82466 .00005 9.84048E-005 yes
XLOC_000009 treated control OK 5.11344 0.0453474 -6.81713 0.00005 9.84048E-005 9.84048E-005 yes
XLOC_000010 treated control OK 8.49633 1.21619 -0.564379 -32.2551 0.00005 9.84048E-005 yes
XLOC_000011 treated control OK 100.369 8.49633 -0.564379 0.00005 9.84048E-005 9.84048E-005 yes
XLOC_000012 treated control OK 206.885 0.0453474 -6.81713 0.00005 0.00005 9.84048E-005
XLOC_000013 treated control OK 9.63649 1.21619 -0.564379 0.00005 9.84048E-005 9.84048E-005 yes
XLOC_000017 treated control OK 18.764 8.49633 -0.564379 -32.2551 0.00005 9.84048E-005 yes
XLOC_000018 treated control OK 0.878346 0.0453474 -6.81713 0.00005 9.84048E-005 9.84048E-005 yes
XLOC_000019 control control OK 1.21619 1.21619 -0.564379 0.00005 0.00005 9.84048E-005
XLOC_000019 treated control OK 1.21619 0.0453474 -6.81713 -32.2551 9.84048E-005 9.84048E-005 yes
Thanks a Lot ...
-Ateeq Khaliq
1 answer
Use the annotation file (GTF) while running the cuffdiff. If you have multiple GTF files, e.g one from cufflinks and other from standard annotation, use cuffmerge to generate the final version of GTF and use it while running cuffdiff.
If you use GTF file, the gene names will be printed to one of the columns in the final output.
e.g: Cuffdiff output ran with GTF file
test_id gene_id gene locus sample_1 sample_2 status value_1 value_2 log2(fold_change) test_stat p_value q_value significant
ENSMUST00000000001 ENSMUSG00000000001 Gnai3 3:107910197-107949064 SB AB OK 14.2736 14.5269 0.0253732 0.112543 0.8671 0.999385 no
ENSMUST00000000003 ENSMUSG00000000003 Pbsn X:75083239-75098962 SB AB NOTEST 0 0 0 0 1 1 no
ENSMUST00000000010 ENSMUSG00000020875 Hoxb9 11:96132770-96137909 SB AB NOTEST 0 0 0 0 1 1 no
ENSMUST00000000028 ENSMUSG00000000028 Cdc45 16:18780539-18835354 SB AB OK 0.872629 0.902901 0.0492005 0.0316144 0.9662 0.999385 no
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Did you include a GFF/GTF file in the Cuffdiff run? the XLOC ids are that appear if gene annotation is missing..
Hi Roy, yes I have included the file and it looks the following, it has got gen name with Id but couldn't get the same if I am running cummeRbund... I used the following command
My cuffdiff output looks like this
Did you try to remove the first two columns is the cuffdiff output and then run cummRband?
Yes i tried doing that, but no change, its showing the same !!! :(