A common approach in analyzing gene expression profiles was identifying differential expressed genes that are deemed interesting. The enrichment analysis we demonstrated in Disease enrichment analysis vignette were based on these differential expressed genes. This approach will find genes where the difference is large, but it will not detect a situation where the difference is small, but evidenced in coordinated way in a set of related genes. Gene Set Enrichment Analysis (GSEA)1 directly addresses this limitation. All genes can be used in GSEA; GSEA aggregates the per gene statistics across genes within a gene set, therefore making it possible to detect situations where all genes in a predefined set change in a small but coordinated way. Since it is likely that many relevant phenotypic differences are manifested by small but consistent changes in a set of genes.
Genes are ranked based on their phenotypes. Given a priori defined set of gens S (e.g., genes shareing the same DO category), the goal of GSEA is to determine whether the members of S are randomly distributed throughout the ranked gene list (L) or primarily found at the top or bottom.
There are three key elements of the GSEA method:
We implemented GSEA algorithm proposed by Subramanian1. Alexey Sergushichev implemented an algorithm for fast GSEA analysis in the fgsea2 package.
In DOSE3, user can use GSEA algorithm implemented in DOSE
or fgsea
by specifying the parameter by="DOSE"
or by="fgsea"
. By default, DOSE use fgsea
since it is much more fast.
Leading edge analysis reports Tags
to indicate the percentage of genes contributing to the enrichment score, List
to indicate where in the list the enrichment score is attained and Signal
for enrichment signal strength.
It would also be very interesting to get the core enriched genes that contribute to the enrichment.
DOSE supports leading edge analysis and report core enriched genes in GSEA analysis.
gseDO
fuctionIn the following example, in order to speedup the compilation of this document, only gene sets with size above 120 were tested and only 100 permutations were performed.
library(DOSE)
data(geneList)
y <- gseDO(geneList,
nPerm = 100,
minGSSize = 120,
pvalueCutoff = 0.2,
pAdjustMethod = "BH",
verbose = FALSE)
head(y, 3)
## ID Description setSize enrichmentScore
## DOID:1492 DOID:1492 eye and adnexa disease 459 -0.3105160
## DOID:5614 DOID:5614 eye disease 450 -0.3125247
## DOID:374 DOID:374 nutrition disease 313 -0.3421127
## NES pvalue p.adjust qvalues rank
## DOID:1492 -1.399095 0.01204819 0.08718993 0.04325883 1793
## DOID:5614 -1.412086 0.01234568 0.08718993 0.04325883 1768
## DOID:374 -1.512394 0.01298701 0.08718993 0.04325883 1464
## leading_edge
## DOID:1492 tags=22%, list=14%, signal=19%
## DOID:5614 tags=22%, list=14%, signal=19%
## DOID:374 tags=22%, list=12%, signal=20%
## core_enrichment
## DOID:1492 3371/3082/5914/2878/4153/3791/23247/1543/80184/6750/1958/2098/7450/596/9187/2034/482/948/1490/1280/3931/5737/4314/4881/2261/3426/187/629/6403/7042/6785/7507/2934/5176/4060/1277/7078/5950/2057/727/10516/4311/2247/1295/358/10203/2192/582/10218/57125/3485/585/1675/6310/2202/4313/2944/4254/3075/1501/2099/3480/4653/1195/6387/3305/1471/857/4016/1909/4053/6678/1296/7033/4915/55812/1191/5654/10631/2152/2697/7043/2952/6935/2200/3572/7177/7031/3479/2006/10451/9370/771/3117/125/652/4693/5346/1524
## DOID:5614 3082/5914/2878/4153/3791/23247/1543/80184/6750/1958/2098/7450/596/9187/2034/482/948/1490/1280/3931/5737/4314/4881/2261/3426/187/629/6403/7042/6785/7507/2934/5176/4060/1277/7078/5950/2057/727/10516/4311/2247/1295/358/10203/2192/582/10218/57125/3485/585/1675/6310/2202/4313/2944/4254/3075/1501/2099/3480/4653/6387/3305/1471/857/4016/1909/4053/6678/1296/7033/4915/55812/1191/5654/10631/2152/2697/7043/2952/6935/2200/3572/7177/7031/3479/2006/10451/9370/771/3117/125/652/4693/5346/1524
## DOID:374 2169/1490/7840/4887/4314/595/4018/6403/590/3087/866/66036/5919/5176/3953/164656/5950/2638/2166/5243/5468/5108/10560/4023/3485/7350/3952/1149/585/1513/3489/79068/4671/477/4313/3625/9369/6720/7494/2099/3480/3991/23446/6678/4915/5167/8228/165/2152/185/367/4982/3667/4128/9607/3572/150/563/1489/3479/9370/9122/5105/2167/5346/79689/5241
gseNCG
fuctionncg <- gseNCG(geneList,
nPerm = 100,
minGSSize = 120,
pvalueCutoff = 0.2,
pAdjustMethod = "BH",
verbose = FALSE)
ncg <- setReadable(ncg, 'org.Hs.eg.db')
head(ncg, 3)
## ID Description setSize enrichmentScore NES pvalue
## lung lung lung 173 -0.3880662 -1.593892 0.01562500
## breast breast breast 133 -0.4869070 -1.951255 0.01587302
## lymphoma lymphoma lymphoma 188 0.2999589 1.331374 0.02777778
## p.adjust qvalues rank leading_edge
## lung 0.04761905 0.02506266 2775 tags=31%, list=22%, signal=25%
## breast 0.04761905 0.02506266 2930 tags=33%, list=23%, signal=26%
## lymphoma 0.05555556 0.02923977 2087 tags=21%, list=17%, signal=18%
## core_enrichment
## lung SETD2/ATXN3L/LRP1B/BRD3/ARID1A/INHBA/RB1/ADCY1/LYRM9/NF1/CTNNB1/TP53/SATB2/STK11/CTIF/CTNNA3/KDR/COL11A1/FLT3/APC/ADGRL3/FGFR3/NCAM2/DIP2C/APLNR/SLIT2/EPHA3/RUNX1T1/ZMYND10/ZFHX4/GLI3/TNN/PLSCR4/DACH1/ERBB4
## breast KMT2A/ERBB3/SETD2/ARID1A/GPS2/NCOR1/RB1/MAP2K4/NF1/TP53/PIK3R1/STK11/CDKN1B/PTGFR/APC/CCND1/TRAF5/MAP3K1/ESR1/TBX3/FOXA1/GATA3
## lymphoma DUSP2/EZH2/PRDM1/MYC/ZWILCH/IKZF3/PLCG2/IDH2/HIST1H1C/MAGEC3/CD79B/ETV6/HIST1H1E/HIST1H1B/IRF8/CD28/SLC29A2/DUSP9/TNFAIP3/DNMT3A/SYK/TNF/BCR/HIST1H1D/DSC3/UBE2A/PABPC1
gseDGN
fuctiondgn <- gseDGN(geneList,
nPerm = 100,
minGSSize = 120,
pvalueCutoff = 0.2,
pAdjustMethod = "BH",
verbose = FALSE)
dgn <- setReadable(dgn, 'org.Hs.eg.db')
head(dgn, 3)
## ID Description setSize
## umls:C0011581 umls:C0011581 Depressive disorder 464
## umls:C0043094 umls:C0043094 Weight Gain 210
## umls:C0024668 umls:C0024668 Mammary Neoplasms, Experimental 192
## enrichmentScore NES pvalue p.adjust qvalues
## umls:C0011581 -0.2963136 -1.279482 0.01282051 0.1173709 0.07769816
## umls:C0043094 -0.3798961 -1.560773 0.01333333 0.1173709 0.07769816
## umls:C0024668 -0.3560902 -1.437279 0.01351351 0.1173709 0.07769816
## rank leading_edge
## umls:C0011581 2587 tags=25%, list=21%, signal=21%
## umls:C0043094 2016 tags=25%, list=16%, signal=21%
## umls:C0024668 2060 tags=27%, list=16%, signal=23%
## core_enrichment
## umls:C0011581 ETS2/HDAC5/RGN/GRIA1/PTGS1/PDE4A/SNCA/ADAMTS2/EHD3/NR5A1/SORCS3/CRY1/ADRB2/FZD1/MYOM2/ADCY1/POU6F1/MAPK3/BICC1/SLC6A4/AHI1/TP53/RNF103/SLC12A2/BDNF/NR3C1/SRSF5/PCLO/GABRA6/WWC1/IL5/GLUL/ELK3/GAD1/RARA/GRM5/KDR/ASAH1/IMPACT/CHRM2/WFS1/TSPAN31/HP/PVALB/HTR1A/BCL2/GPM6A/CYP2A6/DUSP1/NLGN4Y/F2R/CD36/NGFR/NPY2R/DBH/BECN1/CCND1/OXTR/SGCE/SELP/NGF/LPAR1/NRP1/AVPR1B/IFT88/ARSD/FAAH/NEFL/FGF2/CD1C/ABCB1/SRPX/RAPGEF3/CRHBP/HSPA2/LEP/FTO/PER2/ALPK1/GSTM1/DIXDC1/XBP1/ESR1/IGF1R/NTF3/CACNA1C/NR3C2/SLC18A2/NTRK2/SPDEF/RAPGEF4/ALB/NPY1R/F3/AGTR1/TAC1/AR/UCN/FBN1/MAOA/CARTPT/TAT/ADRA2A/MUC1/TGFBR3/TPH1/IGF1/ABAT/MAOB/ADIPOQ/TBC1D9/ADH1B/CRY2/GATA3/TFAP2B
## umls:C0043094 BDNF/NR3C1/ADCY2/VPS13D/CREBBP/GLUL/NID1/GAD1/GRM5/HTR1A/GLUD1/HDC/CD36/DBH/SIPA1L1/OSBPL8/PALLD/FGF1/BCHE/CAVIN1/GSN/APBB2/LEPR/ARHGEF12/FAAH/ABCB1/PPARG/LPL/FSTL1/SORBS2/LEP/HNMT/FTO/FBLN2/SREBF1/CAV1/SPARC/SLC18A2/NTRK2/HTR2B/SETBP1/GRIA2/MAOA/ADRA2A/TPH1/IGF1/SLC1A1/RAMP2/MAOB/ADIPOQ/PLIN1
## umls:C0024668 SLC12A2/MRC2/ID3/PIK3R1/NCOA1/KDR/CDKN1B/STAT5A/TNFSF10/BCL2/S1PR1/COL18A1/G0S2/MMP3/CCND1/GATM/MGP/TSC22D1/ID1/LIN7A/ID4/GSN/RBP4/SELENOP/DUSP6/AQP1/LPL/TRPS1/DIO1/LEP/PRLR/EFEMP1/MMP2/TXNIP/PLK2/KITLG/ESR1/PTN/COL5A1/AFP/ALCAM/AGTR1/IL6ST/TFF1/IGF1/ADIPOQ/FABP4/STC2/GATA3/PGR
cnetplot(ncg, categorySize="pvalue", foldChange=geneList)
enrichMap(y, n=20)
gseaplot(y, geneSetID = y$ID[1], title=y$Description[1])
1. Subramanian, A. et al. Gene set enrichment analysis: A knowledge-based approach for interpreting genome-wide expression profiles. Proceedings of the National Academy of Sciences of the United States of America 102, 15545–15550 (2005).
2. S., A. An algorithm for fast preranked gene set enrichment analysis using cumulative statistic calculation. biorxiv doi:10.1101/060012
3. Yu, G., Wang, L.-G., Yan, G.-R. & He, Q.-Y. DOSE: An r/bioconductor package for disease ontology semantic and enrichment analysis. Bioinformatics 31, 608–609 (2015).