Dear Kevin
Thanks for this detail. I am not a bioloigst. Therefore it not easy for me to correlate results with hypothesis, I am working on. Thank you giving a clue here. :)
Archana
Hello everyone
I want to predict immunogenic signatures in my gene list. I downloaded immunogenicsignature list from http://software.broadinstitute.org/gsea/msigdb/ and performed enrichment using my gene list. As a result, I am getting enrichment of some of the IDs with fdr 0.05 . IDs list is given below
GSE29949_MICROGLIA_BRAIN_VS_CD8_POS_DC_SPLEEN_DN GSE29618_PDC_VS_MDC_DN GSE21670_UNTREATED_VS_TGFB_TREATED_STAT3_KO_CD4_TCELL_DN GSE17721_0.5H_VS_4H_CPG_BMDC_DN GSE21360_PRIMARY_VS_TERTIARY_MEMORY_CD8_TCELL_DN GSE22611_MUTANT_NOD2_VS_CTRL_TRANSDUCED_HEK293T_CELL_UP GSE24726_WT_VS_E2_2_KO_PDC_DAY4_POST_DELETION_UP GSE37301_MULTIPOTENT_PROGENITOR_VS_GRAN_MONO_PROGENITOR_DN GSE7831_UNSTIM_VS_INFLUENZA_STIM_PDC_4H_UP GSE26488_CTRL_VS_PEPTIDE_INJECTION_OT2_THYMOCYTE_DN GSE29164_DAY3_VS_DAY7_UNTREATED_MELANOMA_UP
How can I make some interpretation from above IDs ?? I am just having diffiulty to understand this result ?? I am looking for just simple explanation of this result.
I will appreciate all the suggestions.
Thank you in advance
Hey,
Taking just one example from the above: GSE21360_PRIMARY_VS_TERTIARY_MEMORY_CD8_TCELL_DN:
What it means is that there was some study performed ( by these guys: Repetitive antigen stimulation induces stepwise transcriptome diversification but preserves a core signature of memory CD8(+) T cell differentiation ) where a number of genes were identified as statistically significantly down-regulated in tertiary CD8 memory T-cells when comparing [the tertiary cells] to primary CD8 memory T-cells.
It follows that, through enrichment of your input genes, there was a statistically significant 'overlap' between your genes and those identified as down-regulated in tertiary CD8 memory T-cells in the cited study.
More information here: Gene Set: GSE21360_PRIMARY_VS_TERTIARY_MEMORY_CD8_TCELL_DN
Trust that this helps.
Kevin
Dear Kevin
Thanks for this detail. I am not a bioloigst. Therefore it not easy for me to correlate results with hypothesis, I am working on. Thank you giving a clue here. :)
Archana
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