psygenet2r: An R package for querying PsyGeNET and to perform comorbidity studies in psychiatric disorders
1 November 2022
Package
psygenet2r 1.30.0
1 Introduction
The psygenet2r package contains functions to query PsyGeNET [1], a resource on psychiatric diseases and their genes. This can also be done using the web tool. However, the psygenet2r package goes a step further including analysis and visualization functions to study psychiatric diseases, their genes and disease comorbidities, as well as analyzing the tissues/anatomical structures in which the genes are expressed. A special focus is made on visualization of the results (not web available), providing a variety of representation formats such as networks, heatmaps and barplots (Table 3).
1.1 Background
During the last years there has been a growing interest in the genetics of psychiatric disorders, leading to a concomitant increase in the number of publications that report these studies [2]. However, there is still limited understanding on the celular and molecular mechanisms leading to psychiatric diseases, which has limited the application of this wealth of data in the clinical practice. This situation also applies to psychiatric comorbidities. Some of the factors that explain the current situation is the heterogeneity of the information about psychiatric disorders and its fragmentation into knowledge silos, and the lack of resources that collect these wealth of data, integrate them, and supply the information in an intuitive, open access manner to the community. PsyGeNET has been developed to fill this gap. psygenet2r has been developed to facilitate statistical analysis of PsyGeNET data, allowing its integration with other packages available in R to develop data analysis workflows.
PsyGeNET is a resource for the exploratory analysis of psychiatric diseases and their associated genes. The second release of PsyGeNET (version 2.0) contains updated information on depression, bipolar disorder, alcohol use disorders and cocaine use disorders, and has been expanded to cover other psychiatric diseases of interest: bipolar disorder, schizophrenia, substance-induced depressive disorder and psychoses and cannabis use disorder (Table 1). PsyGeNET allows the exploration of the molecular basis of psychiatric disorders by providing a comprehensive set of genes associated to each disease. Moreover, it allows the analysis of the molecular mechanisms underlying psychiatric disease comorbidities.
| Long Name | Short Name | Acronym |
|---|---|---|
Alcohol use disorders |
Alcohol UD | AUD |
Bipolar disorders and related disorders |
Bipolar disorder | BD |
Depressive disorders |
Depression | DEP |
Schizophrenia spectrum and other psychotic disorders |
Schizophrenia | SCHZ |
Cocaine use disorders |
Cocaine UD | CUD |
Substance induced depressive disorder |
SI-Depression | SI-DEP |
Cannabis use disorders |
Cannabis UD | CanUD |
Substance induced psychosis |
SI-Psychosis | SI-PSY |
PsyGeNET database is the result of the data extracted from the literature by text mining using BeFree [3], followed by manual curation by domain experts. A team of 22 experts participates as curators of the database. The current version of PsyGeNET (version 2.0) contains 3,771 associations between 1,549 genes and 117 psychiatric disease concepts.
With psygenet2r package the user is able to submit queries to PsyGeNET from R, perform a variety of analysis on the data, and visualize the results through different types of graphical representations.
The tasks that can be performed with psygenet2r package are the following:
- Retrieve Gene-Disease Associations (GDAs) from PsyGeNET using as query a gene or a disease (single or a set of genes/diseases) of interest
- Visualize the results according to the GDAs’ attributes: PsyGeNET Evidence Index, number of publications, sentences that report the GDA, source dadatabase
- Visualize the results according to the disease (disease class) or gene (Panther class) attributes
- Analyze the association between two diseases based on shared genes (using the Jaccard index)
- Characterizing the disease genes by molecular function using Panther classes or expression site using TopAnat / Bgee database.
In the following sections the specific functions that can be used to address each of these tasks are presented.
1.2 Installation
The package psygenet2r is provided through Bioconductor. To install psygenet2r the user must type the two following commands in an R session:
if (!requireNamespace("BiocManager", quietly=TRUE))
install.packages("BiocManager")
BiocManager::install( "psygenet2r" )library( psygenet2r )1.3 DataGeNET.Psy
DataGeNET.Psy object is obtained when psygenetGene and psygenetDisease functions are applied. This object is used as input for the rest of psyGeNET2r functions, like the plot function.
DataGeNET.Psy object contains all the information about the different diseases/genes associated with the gene/disease of interested retrieved from PsyGeNET. This object contains a summary of the search, such as the search input (gene or disease), the selected database, the gene or disease identifier, the number of associations found (N. Results) and the number of unique results obtained (U. Results).
t1## Object of class 'DataGeNET.Psy'
## . Type: gene
## . Database: ALL
## . Term: 4852
## . Number of Results: 13
## . Number of unique Diseases: 13
## . Number of unique Genes: 1class( t1 )## [1] "DataGeNET.Psy"
## attr(,"package")
## [1] "psygenet2r"This object comes with a series of functions to allow users to interact with the information retrieved from PsyGeNET. These functions are ngene, ndisease, extract and plot. The first function ngene returns the number of retrieved genes for a given query. ndisease is the homologous function but for the diseases. The function extract returns a formatted data.frame with the complete set of information downloaded from PsyGeNET. Finally, the plot function allows the visualization of the results in a variety of ways such as gene-disease association networks or heatmaps.
3 PsyGeNET and psygenet2r
The PsyGeNET web interface can be explored by searching a specific gene or a specific disease, and psygenet2r package has the same options. Therefore, the starting point for psygenet2r are psygenetGene and psygenetDisease functions.
PsyGeNET data is classified according to the database used as a source of information (“source database”). Therefore, any query run on PsyGeNET requires to specify the source database using the argument called database. Table (tab:psygenet-databases) shows the source databases in PsyGeNET and their description. By default, the database "ALL" is used in psygenet2r. For illustrating purposes along the vignette, database `ALL} will be used in most of code snippets.
| Name | Description |
|---|---|
psycur15 |
Genes associated to DEP, BD, AUD and CUD between 1980 and 2013 (PsyGeNET release v1.0) |
psycur16 |
Genes associated to DEP, BD, AUD, CUD, SCHZ, S-DEP, CanUD and D-PSY between 1980 and 2015 |
ALL |
All previous Databases |
2 Retrieve gene-disease associations (GDAs) using psygenet2r
2.1 Using genes as a query
psygenet2r package allows exploring PsyGeNET information using a specifc gene or a list of genes. It retrieves the information that is available in PsyGeNET (associated diseases, source database, PsyGeNET Evidence Index, number of publications, attributes of genes, etc) and allows to visualize the results in different ways.
2.1.1 Using as a query a single gene
In order to look for a single gene into PsyGeNET, we can use the psygenetGene function. This function retrieves PsyGeNET’s information using both, the NCBI gene identifier and the official Gene Symbol from HUGO. It contains also other arguments like the database to query, the PsyGeNET evidence index (evidenceIndex argument).
As an example, the gene NPY, whose entrez id is 4852 is queried using psygenetGene function, and using alternatively the official HUGO Gene Symbol. In this example database "ALL".
t1 <- psygenetGene( gene = 4852,
database = "ALL")
t1## Object of class 'DataGeNET.Psy'
## . Type: gene
## . Database: ALL
## . Term: 4852
## . Number of Results: 13
## . Number of unique Diseases: 13
## . Number of unique Genes: 1t2 <- psygenetGene( gene = "NPY",
database = "ALL" )
t2## Object of class 'DataGeNET.Psy'
## . Type: gene
## . Database: ALL
## . Term: NPY
## . Number of Results: 13
## . Number of unique Diseases: 13
## . Number of unique Genes: 1Both cases result in an DataGeNET.Psy object:
class( t1 )## [1] "DataGeNET.Psy"
## attr(,"package")
## [1] "psygenet2r"class( t2 )## [1] "DataGeNET.Psy"
## attr(,"package")
## [1] "psygenet2r"In the particular example used, by inspecting the DataGeNET.Psy object, we can see that the gene NPY is associated to 13 different diseases in PsyGeNET (with no restriction on the PsyGeNET evidence index).
2.1.2 Ploting the results of a Single Gene Query
psygenet2r offers several options to visualize the results from PysGeNET in networks by changing the type argument when applying the plot function. A network showing the diseases (type = "GDA network") or the psychiatric disorders (type = "GDCA network") related to the gene of interest is obtained.
By default, psygenet2r shows a network when ploting a DataGeNET.Psy object obtained by a gene-query. The result is a network where blue nodes are diseases and the yellow node is the gene of interest. Node colors can be changed adding the following arguments geneColor and diseaseColor.
plot( t1, type = "GDA network" )
On the other hand, results can be visualized according to the 8 psychiatric disorders classes available in PsyGeNET (depression, bipolar disorder, alcohol use disorders, cocaine use disorder, bipolar disorder, schizophrenia, cannabis use disorder, substance-induced depressive disorder and psychoses) setting the type argument to "GDCA network". As a result, a network with a maximum of 9 nodes is obtained (8 nodes that represent the psychiatric disorders and 1 node that represents the gene). The node’s size of each psychiatric disorder is proportional to the number of disease concepts that belongs to each disease class, from the total number of diseases associated to the gene.
Note that the node colors can be changed adding the next arguments: AUDcolor for alcohol use disorders node, BDcolor for bipolar disorders and related disorders node, DEPcolor for depressive disorders node, SCHZcolor for schizophrenia spectrum and other psychotic disorders node, CUDcolor for cocaine use disorders node, SIDEPcolor for substance induced depressive disorder node, CanUDcolor for cannabis use disorders node, SYPSYcolor for substance induced psychosis node and geneColor for the gene node.
plot( t1, type = "GDCA network" )
In our example, NPY is associated to four of the eight psychiatric disorders present in PsyGeNET, with an important contribution of depression.
2.1.3 Using as a query a list of genes
In the same way, psygenet2r allows to query PsyGeNET given a list of genes of interest. The same function, psygenetGene, accepts a vector of NCBI gene identifiers or HUGO official gene symbols.
To illustrate this functionality, a list of 20 genes was extracted from the article entitled “The Genetics of Major Depression” [4], where these genes are associated to depression. The vector of genes can be defined as follows:
genesOfInterest <- c( "COMT", "CLOCK", "DRD3", "GNB3", "HTR1A",
"MAOA", "HTR2A","HTR2C", "HTR6", "SLC6A4", "ACE", "BDNF",
"DRD4", "HTR1B", "HTR2B", "HTR2C", "MTHFR", "SLC6A3", "TPH1",
"SLC6A2", "GABRA3"
)Then, the function psygenetGene is applied. In this case an extra argument called verbose was set to TRUE. This shows some information during the query-process, for example the message informing that there are repeated genes in the list (the gene HTR2C was placed twice in the list to raise this message) and the message informing that one or more of the given genes is not in PsyGeNET (in this case the gene HTR2B).
m1 <- psygenetGene(
gene = genesOfInterest,
database = "ALL",
verbose = TRUE
)## Warning in psygenetGene(gene = genesOfInterest, database = "ALL", verbose =
## TRUE): Removing duplicates from input genes list.## Staring querying PsyGeNET for COMT, CLOCK, DRD3, GNB3, HTR1A, MAOA, HTR2A, HTR2C, HTR6, SLC6A4, ACE, BDNF, DRD4, HTR1B, HTR2B, MTHFR, SLC6A3, TPH1, SLC6A2, GABRA3 in ALL database.## Warning in psygenetGene(gene = genesOfInterest, database = "ALL", verbose = TRUE): One or more of the given genes is not in PsyGeNET ( 'ALL' ):
## HTR2BA DataGeNET.Psy object is obtained. In this particular example, 19 genes are present in PsyGeNET and are associated to 42 diseases, involving 212 GDAs.
m1## Object of class 'DataGeNET.Psy'
## . Type: gene
## . Database: ALL
## . Term: COMT ... GABRA3
## . Number of Results: 212
## . Number of unique Diseases: 42
## . Number of unique Genes: 192.1.4 Ploting the results of the query using a list of genes
psygenet2r provides several options to visualize the results of these queries, such as networks, heatmaps and barplots.
As for the single gene example, the default option in psygenet2r results is a network chart, where the blue nodes represent diseases and the yellows nodes represent genes. Node colors can be changed adding the following arguments geneColor and diseaseColor.
plot( m1 )
It is also possible to visualize the results by grouping the diseases according to the psychiatric disorders present in PsyGeNET (depression, bipolar disorder, alcohol use disorders, cocaine use disorder, bipolar disorder, schizophrenia, cannabis use disorder, substance-induced depressive disorder and psychoses) setting the type argument to "GDCA network". As a result, a psychiatric disorder genes network is obtained. The edge’s size is proportional to the number of disease concepts that belongs to each disease class, from the total number of diseases associated to the gene.
Note that the node colors can be changed adding the next arguments: AUDcolor for alcohol use disorders node, BDcolor for bipolar disorders and related disorders node, DEPcolor for depressive disorders node, SCHZcolor for schizophrenia spectrum and other psychotic disorders node, CUDcolor for cocaine use disorders node, SIDEPcolor for substance induced depressive disorder node, CanUDcolor for cannabis use disorders node, SYPSYcolor for substance induced psychosis node and geneColor for the gene node.
plot( m1, type = "GDCA network" )
psygenet2r package allows to visualize the GDAs attributes in a heatmap. The argument type must be "GDA heatmap" and the PsyGeNET evidence index can also be determined by the user setting the cut-off argument to the evidence index of interest. In this example, the cut-off is set to 0, in order to obtain all the results. If we set the cut-off to 0.5, only those associations with at least half of the publications supporting the association will be shown. In this kind of representation we can identify genes that are associated to several diseases (e.g. SLC6A4), others that are associated only to one disease (e.g. HTR6) and we can visualize the evidence index for each association.
Note that heatmap cells are coloured by default in blue, grey or yellow. Blue cells represent those GDAs where all the evidences reviewed by the experts support the existence of an association between the gene and the disease (EI = 1); it will be grey when there is contradictory evidence for the GDA (some publications support the association while others publications do not support it, 1 > EI > 0), and it will be yellow when all the evidences reviewed by the experts report that there is no association between the gene and the disease (EI = 0).
The heatmap cells colors can be changed using the arguments ei0color for those cases in which EI = 0, eiAmbiguitcolor for those cases in which 1 > EI > 0 and ei1color for those cases in which EI = 1.
plot( m1, type="GDA heatmap" )
In this example we can see that there are 3 GDAs in yellow (GNB3-chronic alcoholic intoxication; HTR2A-drug psychoses and ACE-major affective disorder 2), indicating that all publications report that there is no association.
An alternative graphical representation is a psychiatric disorder heatmap related to the percentage of diseases in a class to which a gene is associated. It allows to analyze if the genes that are being studied present a specific association with a subtype of disorder or if they are associated with several of them in the same psychiatric disorder class. The percentage of diseases to which a gene appears associated with each psychiatric disorder is estimated. This percentage is relative to the total number of subtypes of disorders present in PsyGeNET (33 for alcohol UD, 9 for bipolar disorder, 37 for depression, 24 for schizophrenia, 6 for cocaine UD, 3 for cannabis UD, 3 for DI-Psychosis and 2 for SI-Depression). The resulting values are represented in a heatmap according to a blue color scale.
In order to obtain this graphic, type must be set to "GDCA heatmap". The resulting heatmap shows which are the genes that are higher or lower associated to each one of the psychiatric disorders. Note that the heatmap colors can be defined using the arguments highColor (blue by default) and ‘lowColor’ (white by default).
plot( m1, type = "GDCA heatmap" )
As it could be expected for the genes that are used in this query, all of them are associated to depression, to a greater or lesser extent. Some of them are also associated to the other six psychiatric disorders, following a similar pattern alcohol UD and bipolar disorder.
psygenet2r package also allows to analyze a gene list according to the function of the proteins encoded by these genes. The PANTHER Protein Class Ontology classifies proteins according to their function.
The pantherGraphic function shows the Panther class of the proteins for each psychiatric disorder class. It provides a graphic with the results of these analysis, being the input a list of genes and the database (ALL, psycur15, psycur16). The input genes can be from a vector that contains the genes of interest, or from the genes obtained in the DataGeNET.psy object in a disease or disease-list query. Given the vector with the genes of interest, this function creates a representation of the panther-class these genes belong to. The sum of the percentages of the different protein class for each specific psychiatric disease will be 100%. Note that this percentage will be relative to the number of the input genes associated with each psychiatric category. A evidenceIndex argument can be added to filter results. It can also be done given a DataGeNET.psy object obtained by querying with a single gene.
genesOfInterest <- unique( genesOfInterest )
pantherGraphic( genesOfInterest, "ALL" )## Warning in psygenetGene(geneList, database, verbose = verbose): One or more of the given genes is not in PsyGeNET ( 'ALL' ):
## HTR2B
psygenet2r offers additional options to visualize the results of a query using a list of genes or from the genes obtained in the DataGeNET.psy object in a gene or gene-list query. Barplots and pie charts showing the gene attributes can be obtained by applying the geneAttrPlot function.
psygenet2r package allows to visualize how many of our genes of interest are associated to each psychiatric disorder present in PsyGeNET and how many of them are exclusively associated to a particular psychiatric disorder. This can be done applying the geneAttrPlot function and setting the type argument to "cateogry".
geneAttrPlot( m1, type = "disease category" )
As a result, a barplot is obtained. The X axis contains the psychiatric disorders, sorted alphabetically and the number of genes are represented in the Y axis. For each psychiatric disorder two bars are plotted, the blue bar represents the total number of genes for the psychiatric disorder. For those cases in which some of these genes are specific for the disorder according to PsyGeNET, a second bar coloured in orange will be displayed. The bar colors can be changed using the arguments totalGenesBarColor and uniqueGenesBarColor respectively.
Alternatively, psygenet2r package allows to visualize for each gene, how many disease concepts and how many psychiatric categories are associated to it. This can be done applying the geneAttrPlot function and setting the type argument to "gene".
geneAttrPlot( m1, type = "gene" )
As a result, a barplot is obtained. The X axis contains the genes, sorted alphabetically and the number of cuis and psychiatric categories are represented in the Y axis. For each psychiatric disorder two bars are plotted, the purple bar represents the number of cuis and the yellow one belongs to the number of categories. The bar colors can be changed using the arguments cuiBarColor and diseaseCategoryBarColor respectively.
In our example, the gene SLC6A4 is the one whith more associated cuis (26) and categories (6).
If we are only interested in how many of our input genes are associated to each disease category, psygenet2r package allows to visualize it in a pie chart by applying the geneAttrPlot function and setting up the type argument to pie.
Note that the colors for each psychiatric category can be changed adding the next arguments: AUDcolor for alcohol use disorders, BDcolor for bipolar disorders and related disorders, DEPcolor for depressive disorders, SCHZcolor for schizophrenia spectrum and other psychotic disorders, CUDcolor for cocaine use disorders, SIDEPcolor for substance induced depressive disorder, CanUDcolor for cannabis use disorders and SYPSYcolor for substance induced psychosis.
geneAttrPlot( m1, type = "pie" )
In our example, depression has 19 associated genes, and the majority of them are also associated to other psychiatric disorders, like bipolar disorder (18 genes) and alcohol UD (16 genes).
In PsyGeNET it is important to keep track of both “positive” and the “negative” findings, and let the user make their own judgements based on the available evidence. Thus, for each GDA and each supporting publication,the association type information is provided. According to the evidence, there are two types: “Association” and “No Association” (e.g. the “negative findings”).
psygenet2r package allows to visualize this information in a barplot. It can be done by applying the geneAttrPlot function and setting the type argument to "evidence index". As a result a barplot showing, for each psychiatric disorder, how many gene-disease association are in total (red bar), how many of them are 100% association (green bar), 100% no association (blue bar) and how many GDAs are supported by both association types (purple bar).
geneAttrPlot( m1, type = "evidence index" )
In our example, the barplot shows that depression is the psychiatric disorder with more gene-disease associations (127 GDAs), and there is no negative evidence for any of the associations.
2.1.5 Enrichment analysis for a list of genes
The R package psygenet2r allows to perform an enrichment analysis on a list of genes with PsyGeNET diseases. It is done by using the function enrichedPD. In order to illustrate this function, the previous list of 20 genes associated to depression [4] will be used.
tbl <- enrichedPD( genesOfInterest, database = "ALL")
tbl## MPD
## Alcohol use disorders Alcohol use disorders
## Depressive disorders Depressive disorders
## Bipolar disorders and related disorders Bipolar disorders and related disorders
## Cocaine use disorders Cocaine use disorders
## Schizophrenia spectrum and other psychotic disorders Schizophrenia spectrum and other psychotic disorders
## Cannabis use disorders Cannabis use disorders
## Substance induced psychosis Substance induced psychosis
## Substance induced depressive disorder Substance induced depressive disorder
## p.value
## Alcohol use disorders 1.873960e-08
## Depressive disorders 6.286367e-09
## Bipolar disorders and related disorders 2.559998e-08
## Cocaine use disorders 3.697393e-07
## Schizophrenia spectrum and other psychotic disorders 8.854607e-01
## Cannabis use disorders 3.406556e-03
## Substance induced psychosis 1.737779e-02
## Substance induced depressive disorder 1.361419e-02The result is a table with a p-value of the enrichment of the given list of genes for each psychiatric disorder in PsyGeNET. As we can see, if we put a p-value cut-off of 0.01, these genes are enriched in 5 of the 8 psychiatric disorders, being alcohol UD (p-val ~ 9e-10) and depression (p-val ~ 6e-9), the ones with the lowest p-value.
2.1.6 Enrichment analysis based on anatomical terms (TopAnat) for a list of genes
psygenet2r package allows to perform gene set enrichment test based on expression of genes in anatomical structures, importing data from the Bgee database [5] and importing functions from BgeeDB R package [6] .
It is done by using the function topAnatEnrichment. This function perform the enrichment analysis using a list of genes (NCBI gene identifier or official Gene Symbol from HUGO). It contains also other arguments like the dataType (rna_seq or affymetrix), statistics, that by default is fisher and the cutOff argument.
tpAnat <- topAnatEnrichment( genesOfInterest, cutOff = 1 )head( tpAnat )## organId organName annotated significant
## UBERON:0000013 UBERON:0000013 sympathetic nervous system 338 5
## UBERON:0000407 UBERON:0000407 sympathetic trunk 338 5
## UBERON:0002410 UBERON:0002410 autonomic nervous system 338 5
## UBERON:0001769 UBERON:0001769 iris 182 3
## UBERON:0011892 UBERON:0011892 anterior uvea 187 3
## UBERON:0001697 UBERON:0001697 orbital region 117 2
## expected foldEnrichment pValue FDR
## UBERON:0000013 3.75 1.333333 0.3141495 1
## UBERON:0000407 3.75 1.333333 0.3141495 1
## UBERON:0002410 3.75 1.333333 0.3141495 1
## UBERON:0001769 2.02 1.485149 0.3278057 1
## UBERON:0011892 2.07 1.449275 0.3438253 1
## UBERON:0001697 1.30 1.538462 0.3763757 1The result is a data frame that contains the anatomical structures. Results are sorted by p-value, and FDR values are calculated.
2.1.7 Sentences that report a GDA
psygenet2r package also allows to extract the sentences that report a gene-disease asssociation from the supporting publications. It is done by using two different functions, psygenetGeneSentences and extractSentences. psygenetGeneSentences needs as input a gene list and a database to query in. The output of this function is a DataGeNET.Psy object. This object is passed to the extractSentences function, that also needs the disorder of interest.
genesOfInterest## [1] "COMT" "CLOCK" "DRD3" "GNB3" "HTR1A" "MAOA" "HTR2A" "HTR2C"
## [9] "HTR6" "SLC6A4" "ACE" "BDNF" "DRD4" "HTR1B" "HTR2B" "MTHFR"
## [17] "SLC6A3" "TPH1" "SLC6A2" "GABRA3"sss <- psygenetGeneSentences( geneList = genesOfInterest,
database = "ALL")## Warning in psygenetGeneSentences(geneList = genesOfInterest, database = "ALL"):
## One or more of the given genes is not in PsyGeNET ( 'ALL' ). Genes: HTR2Bsss## Object of class 'DataGeNET.Psy'
## . Type: gene
## . Database: ALL
## . Term: COMT ... GABRA3
## . Number of Results: 743
## . Number of unique Diseases: 42
## . Number of unique Genes: 19geneSentences <- extractSentences( object = sss,
disorder = "alcohol abuse")
head(geneSentences)## GENE_SYMBOL GENE_ID DISEASE_UMLS DISEASE_NAME ORIGINAL_DB PUBMED_ID
## 117 DRD3 1814 C0085762 alcohol abuse psycur15 10686561
## 199 HTR1A 3350 C0085762 alcohol abuse psycur15 12753073
## 239 MAOA 4128 C0085762 alcohol abuse psycur15 22030358
## 240 MAOA 4128 C0085762 alcohol abuse psycur15 17347351
## 292 HTR2A 3356 C0085762 alcohol abuse psycur15 18241316
## 293 HTR2A 3356 C0085762 alcohol abuse psycur15 9632223
## ANNOTATION
## 117 Association
## 199 Association
## 239 Association
## 240 Association
## 292 No Association
## 293 Association
## SENTENCE
## 117 We conclude that neither the COMT nor <span class=gene id=10686561-10-38-42>DRD3</span> polymorphisms are associated with anxiety, depression, or <span class=disease id=10686561-10-101-114>alcohol abuse</span>.
## 199 As disturbances of serotonin neurotransmission are implicated in <span class=disease id=12753073-2-65-78>alcohol abuse</span> and aggression, we have examined in BDNF (+/-) mice alcohol drinking behavior, as well as central 5-hydroxytryptamine (5-HT)1A receptor function at the level of <span class=gene id=12753073-2-240-255>5-HT1A receptor</span>-G protein interaction.
## 239 Low-activity <span class=gene id=22030358-10-13-17>MAOA</span> genotype buffered against symptoms of dysthymia, major depressive disorder, and <span class=disease id=22030358-10-98-111>alcohol abuse</span> for sexually abused white participants.
## 240 For example, it has been shown that childhood maltreatment interacts with a <span class=gene id=17347351-8-76-95>monoamine oxidase A</span> (<span class=gene id=17347351-8-97-101>MAOA</span>) gene variant to predict antisocial behavior that is often associated with <span class=disease id=17347351-8-177-187>alcoholism</span>, and an interaction between early life stress and a serotonin transporter promoter variant predicts <span class=disease id=17347351-8-288-301>alcohol abuse</span> in nonhuman primates and depression in humans.
## 292 <span class=disease id=18241316-13-0-13>Alcohol abuse</span> by itself did not have a significant effect on PFC <span class=gene id=18241316-13-65-72>5-HT(2A</span>) binding and as <span class=gene id=18241316-13-89-96>5-HT(2A</span>) binding in alcoholics is not different from controls and antagonists may be therapeutic, fewer receptors may result in downstream developmental effects on the brain resulting in a predisposition to <span class=disease id=18241316-13-296-306>alcoholism</span>.
## 293 Finally, because both the opiate and <span class=gene id=9632223-10-37-43>5-HT2A</span> antagonists reduce the ingestion of saccharin and chocolate solutions differentially, it is apparent that preferences for alternative palatable fluids should be examined when candidate drugs are screened for suppressing alcohol drinking and ultimately the treatment of <span class=disease id=9632223-10-313-326>alcohol abuse</span>.dim( geneSentences )## [1] 14 8The result is a data frame that contains the gene symbol, gene identifier, disease name, original db, the pmid, the annotation type and the sentence.
2.2 Using diseases as a query
psygenet2r package allows to explore PsyGeNET information searching a specifc disease or a list of diseases. As in the case of genes, it retrieves the information that is available in PsyGeNET and allows to visualize the results in several ways.
2.2.1 Using as a query a single disease
In order to look for a single disease into PsyGeNET, psygenet2r has the psygenetDisease function. This function allows you to obtain PsyGeNET’s information using both disease id or disease name, and the database as input (by default is ALL).
If the user does not know the disease identifier, the getUMLS function can be used to obtain disease names and UMLS CUIs from a string query. Providing as input the term and source of interest, getUMLs function retrieves all the PsyGeNET concepts that contain it. As an example it is shown the query results for depressive term in ALL databases.
getUMLs( "depressive", database = "ALL" )## DiseaseName
## 2 depressive symptoms
## 4 major depressive disorder
## 16 depressive disorder
## 103 depressive disorder, treatment-resistant
## 120 drug-induced depressive state
## 186 single major depressive episode
## 658 recurrent depressive disorder, unspecified
## 1043 mixed anxiety and depressive disorder
## 1061 depressive syndrome
## 1091 recurrent major depressive episodes
## 1117 depressive episode, unspecified
## PsychiatricDisorder umls
## 2 Depressive disorders umls:C0086132
## 4 Depressive disorders umls:C1269683
## 16 Depressive disorders umls:C0011581
## 103 Depressive disorders umls:C2063866
## 120 Substance induced depressive disorder umls:C0338715
## 186 Depressive disorders umls:C0024517
## 658 Depressive disorders umls:C0349218
## 1043 Depressive disorders umls:C0338908
## 1061 Depressive disorders umls:C0086133
## 1091 Depressive disorders umls:C0154409
## 1117 Depressive disorders umls:C0349217As an example, the disease major affective disorder 2, whose disease id is umls:C1839839 is queried using psygenetDisease function, and using both, disease name and disease id. The argument evidenceIndex is filled with a vector which first position can be '<' or '>' to indicate if the threshold is read as lower or upper. The second argument is the threshold in itself which will always be included. This argument is also present in psygenetGene.
The the PsyGeNET evidence index (EI) ranges from 0 to 1 (EI = 1, when all the evidences reviewed by the experts support the existence of an association between the gene and the disease; 1 > EI > 0, when there is contradictory evidence for the GDA and EI = 0 when all the evidences reviewed by the experts report that there is no association between the gene and the disease).
For this example database "ALL" and evidenceIndex > 0.5 is selected:
d1 <- psygenetDisease( disease = "umls:C1839839",
database = "ALL",
evidenceIndex = c('>', 0.5 ) )
d1## Object of class 'DataGeNET.Psy'
## . Type: disease
## . Database: ALL
## . Term: umls:C1839839
## . Number of Results: 17
## . Number of unique Genes: 17
## . Number of unique Diseases: 1d2 <- psygenetDisease( disease = "major affective disorder 2",
database = "ALL",
evidenceIndex = c('>', 0.5 ) )
d2## Object of class 'DataGeNET.Psy'
## . Type: disease
## . Database: ALL
## . Term: major affective disorder 2
## . Number of Results: 17
## . Number of unique Genes: 17
## . Number of unique Diseases: 1Both cases result in an DataGeNET.Psy object, that contains the same information as in the gene query search:
class( d1 )## [1] "DataGeNET.Psy"
## attr(,"package")
## [1] "psygenet2r"class( d2 )## [1] "DataGeNET.Psy"
## attr(,"package")
## [1] "psygenet2r"2.2.2 Plotting results of a Single Disease Query
psygenet2r package offers several options to visualize the results from PysGeNET given a disease: a network showing the genes related to the disease of interest and a barplot showing how many publications report each one of the gene-disease associations.
By default, psygenet2r shows the GDAs network when ploting a DataGeNET.Psy object with a disease-query. The result is a network where, yellow nodes are genes and the central and blue node is the disease of interest. Node colors can be changed adding the following arguments geneColor and diseaseColor.
plot ( d1,
geneColor = "turquoise2",
diseaseColor = "black")
2.2.3 Using a list of diseases as a query
In the same way, psygenet2r allows to query PsyGeNET given a set of diseases of interest. The same function, psygenetDisease, accepts a vector of disease-names or disease-ids (umls code).
To illustrate this functionality, two disorders has been selected: chronic schizophrenia and alcohol use disorder. The vector of diseases can be defined for example, as follows:
diseasesOfInterest <- c( "chronic schizophrenia","alcohol use disorder" )tt <- psygenetDisease( disease = diseasesOfInterest,
database = "ALL" )
tt## Object of class 'DataGeNET.Psy'
## . Type: disease
## . Database: ALL
## . Term: chronic schizophrenia ... alcohol use disorder
## . Number of Results: 25
## . Number of unique Genes: 25
## . Number of unique Diseases: 2dm <- psygenetDisease( disease = c( "umls:C0221765", "umls:C0001956" ),
database = "ALL" )
dm## Object of class 'DataGeNET.Psy'
## . Type: disease
## . Database: ALL
## . Term: umls:C0221765 ... umls:C0001956
## . Number of Results: 25
## . Number of unique Genes: 25
## . Number of unique Diseases: 2tm <- psygenetDisease( disease = c( "chronic schizophrenia","umls:C0001956" ),
database = "ALL" )
tm## Object of class 'DataGeNET.Psy'
## . Type: disease
## . Database: ALL
## . Term: chronic schizophrenia ... umls:C0001956
## . Number of Results: 25
## . Number of unique Genes: 25
## . Number of unique Diseases: 2Three cases result in an DataGeNET.Psy object:
class( tt )## [1] "DataGeNET.Psy"
## attr(,"package")
## [1] "psygenet2r"class( dm )## [1] "DataGeNET.Psy"
## attr(,"package")
## [1] "psygenet2r"class( tm )## [1] "DataGeNET.Psy"
## attr(,"package")
## [1] "psygenet2r"This type of object contains all the information about the different genes associated with the diseases of interest retrieved from PsyGeNET. By inspecting the DataGeNET.Psy object we can see that, according to PsyGeNET and querying in ALL databases, the 2 disorders of interest are associated to 25 different genes in 25 different associations.
2.2.4 Ploting results: Multiple Diseases
psygenet2r provides a network graphic and a heatmap to visualize the results of search with multiple input items.
As for single disease, GDAs network is the default option in psygenet2r. In the resulting network chart, the blue nodes represent diseases and the yellows nodes represent genes. Node colors can be changed adding the following arguments geneColor and diseaseColor.
plot( tm )
Another possible option is visualize it in a heatmap. The argument type can be set to "GDCA heatmap".
plot( tm, type = "GDCA heatmap" )
The result is a heatmap where the diseases are located at Y axis, and genes appear at X axis. The color is related to the PsyGeNET evidenceIndex (EI), being blue when EI = 1, yellow when EI = 0 and grey for 0>EI<1. The EI ranges from 0 to 1 (EI=1, when all the evidences reviewed by the experts support the existence of an association between the gene and the disease; 1 > EI > 0, when there is contradictory evidence for the GDA and EI=0 when all the evidences reviewed by the experts report that there is no association between the gene and the disease).
The heatmap cells colors can be changed using the arguments ei0color for those cases in which EI = 0, eiAmbiguitcolor for those cases in which 1 > EI > 0 and ei1color for those cases in which EI = 1.
2.2.5 Barplot according to number of publications that support the GDA
psygenet2r package allows to see how many publications support each gene-disease association. This can be visualized in a barplot by determining the gene or disease id in the name argument and setting type argument to "publications ". The bar color can be changed using the argument barColor (by default grey).
plot( d1,
name = "major affective disorder 2",
type = "publications" )## Warning in xtfrm.data.frame(x): cannot xtfrm data frames
As a result, a barplot is obtained. The X axis contains the genes related to the disease of interest, sorted by the number of pubmed ids in which we can find the gene-disease association. Alternatively, the results can be visualized for the diseases.
plot( t1,
name = "NPY",
type = "publications",
barColor = "blue")## Warning in xtfrm.data.frame(x): cannot xtfrm data frames
3 Analyze the association between two diseases based on shared genes
We can study the association between two diseases from the point of view of shared genetic contribution. More precisely, we can estimate the degree of association of two diseases by means of the number of genes that are shared between the two diseases, over the total number of disease genes. Similarity measures such as the Jaccard Index can be used to estimate disease similarity.
The strategy to calculate the Jaccard Index and its p-value as follows:
- Calculate the Jaccard Index between the pair of diseases. Let’s call it rJI.
- Randomly select a set of genes from DisGeNET for each one of the input diseases (or set of genes) and compute their Jaccard Index (iJI).
- Calculate the p-value by dividing the count of the iJI higher than the real rJI by the number of attempts we performed the step B plus one (
nboot + 1).
3.1 JaccardIndexPsy object
JaccardIndexPsy object is obtained when jaccardEstimation function is applied. The results of this object can be visualized by applying the plot function.
JaccardIndexPsy object contains all the information about the Jaccard estimation characteristics and the results retrieved from PsyGeNET. This object contains a summary of the search, such as the number of iterations used to compute the pvalue associted to the calculated Jaccard Index (\#Boot), the type of search (Type) and the number results obtained (\#Results).
ji1## Object of class 'JaccardIndexPsy'
## . #Boot: 100
## . Type: geneList - disease
## . #Results: 117class( ji1 )## [1] "JaccardIndexPsy"
## attr(,"package")
## [1] "psygenet2r"This object comes with a series of functions to allow users to interact with the information retrieved from PsyGeNET. These functions are extract and plot. The function extract returns a formatted data.frame with the complete set of information downloaded from PsyGeNET. The plot function allows the visualization of the results in a variety of ways such as barplots or heatmaps.
3.2 Using the Jaccard Index
The Jaccard Index, also known as the Jaccard similarity coefficient, is a statistic used for comparing the similarity of two sets, and is defined as the size of the intersection divided by the size of the union of the sample sets:
\[\begin{equation*} J(A, B) = \frac{\mid A \cap B \mid}{\mid A \cup B \mid} \end{equation*}\]
psygenet2r comes with functions to compute the Jaccard Index as an estimation of the similarity of two diseases based on shared genes, given information retrieved from PsyGeNET. The user can compute the Jaccard Index using the function jaccardEstimation. This function accepts multiple inputs:
- Using a list of genes of interest the function will compute the Jaccard Index between the set of genes and all the diseases in PsyGeNET.
genes_interest <- c("SLC6A4", "DRD2", "HTR1B", "PLP1", "TH", "DRD3")
ji1 <- jaccardEstimation(genes_interest, database = "ALL")## Warning in singleInput.genes(diseases$diseases$geneList$genes, psy, universe, :
## Jaccard Index for all diseases in PsyGeNET will be calculated.- Using a list of genes of interest and a list of diseases of interest, the function computes the Jaccard Index between the set of genes and each disease:
disease_interest <-
c("delirium", "bipolar i disorder", "severe depression", "cocaine dependence")
ji2 <- jaccardEstimation(genes_interest, disease_interest, database = "ALL")- With a list of diseases of interest, the function will calculate the Jaccard Index between themselves:
ji3 <- jaccardEstimation(disease_interest, database = "ALL")To determine if the association between two diseases as estimated by the Jaccard Index was statistically significant, we apply a bootstrap procedure to estimate the likelihood of obtaining a Jaccard Index greater than the one obtained for the association between the diseases by chance. In other words, we sample at random gene sets of size n and p (n, p is the number of genes associated to disease 1 and 2, respectively) from a population of human disease genes obtained from DisGeNET [7]. These random gene sets (n and p) are then used to compute the Jaccard Index for diseases 1 and 2. This procedure is repeated by default 100 times. The number of iterations used to compute the pvalue associted to the calculated Jaccard Index can be changed by the user with the nboot argument. Then, we calculated the number of times we obtained a Jaccard Index for the random gene sets larger than the observed value of the Jaccard Index. % We only kept disease associations for which we obtained less than 5/100 random cases an Jaccard Index value larger than the observed one.
The raw results are stored in JaccardIndexPsy and can be obtained using the function extract. For example:
head(extract(ji1))## Disease1 Disease2 NGenes1 NGenes2 JaccardIndex pval
## 1 genes alcoholic intoxication, chronic 6 279 0.01785714 0
## 2 genes depressive disorder 6 276 0.01805054 0
## 3 genes mental depression 6 260 0.01915709 0
## 4 genes alcohol abuse 6 44 0.06382979 0
## 5 genes mood disorders 6 185 0.02688172 0
## 6 genes major depressive disorder 6 254 0.01960784 0tail(extract(ji1))## Disease1 Disease2 NGenes1 NGenes2 JaccardIndex pval
## 50 genes major affective disorder 2 6 23 0.000000000 0.01980198
## 53 genes manic mood 6 6 0.000000000 0.01980198
## 40 genes depressive symptoms 6 30 0.000000000 0.03960396
## 32 genes schizophrenia 6 861 0.001154734 0.06930693
## 30 genes nonorganic psychosis 6 84 0.000000000 0.08910891
## 31 genes psychotic disorders 6 109 0.000000000 0.099009903.3 Plotting results: Jaccard Index
The plot of the result of a `jaccardEstimation} using a singe set of genes corresponds to a bar-plot of the Jaccard Index with each disease:
plot(ji1, cutOff = 0.1)## Warning in xtfrm.data.frame(x): cannot xtfrm data frames
The previous bar-plot shows the Jaccard Index greater than 0.1 obtained from testing each diseases in PsyGeNET. When given a set of genes and a set of diseases, the resulting plot is equivalent:
plot(ji2)## Warning in xtfrm.data.frame(x): cannot xtfrm data frames
Note that the bar colors can be changed using the arguments highColor.
The plot resulting from more than one disease is a heat-map with the given disease as X axis and all the diseases that share genes with them placed as Y axis. The intensity of the color represents the value of the Jaccard Index between, being the darker one the major Jaccard Index. Note that the heatmap colors can be defined using the arguments highColor and ‘lowColor’.
plot(ji3)
4 Warnings
GDCA heatmap type argument do not allow queries for single gene:
> plot( t1, type = "GDCA heatmap" )
==> Error: For this type of chart, a multiple gene query created with
'psygenetGene' is required.5 Summary of Visualization Options
| Input Object | psygenet2r function |
Argument Type | Output Generated |
|---|---|---|---|
DataGeNET.Psy |
geneAttrPlot |
disease category | genes asociated with each DC |
| gene | disease concepts and DC associated with each gene | ||
| pie | pie chart number of genes per DC | ||
| evidence index | barplot showing the type of association | ||
plot |
GDA network | GDA network (default type) | |
| GDCA network | GDCAs network | ||
| GDA heatmap | Evidence Index heatmap for GDCAs (gene) | ||
| GDCA heatmap | Heatmap for GDA (disease) | ||
| publications | number of publications supporting GDA | ||
| Gene vector | pantherGraphic |
/ | Barplot showing the protein panther class |
| JaccardIndexPsy | plot |
/ | JI Bar-plot / heatmap |
Bibliography
1. Gutiérrez-Sacristán A, Grosdidier S, Valverde O, Torrens M, Bravo À, Piñero J, et al. PsyGeNET: a knowledge platform on psychiatric disorders and their genes. Bioinformatics. 2015;31:3075–7. doi:10.1093/bioinformatics/btv301.
2. Sullivan PF, Daly MJ, O’donovan M. Genetic architectures of psychiatric disorders: The emerging picture and its implications. Nature Reviews Genetics. 2012;13:537–51. http://www.nature.com/nrg/journal/v13/n8/full/nrg3240.html.
3. Bravo À, Piñero J, Queralt-Rosinach N, Rautschka M, Furlong LI. Extraction of relations between genes and diseases from text and large-scale data analysis: Implications for translational research. BMC bioinformatics. 2015;16:55. http://bmcbioinformatics.biomedcentral.com/articles/10.1186/s12859-015-0472-9.
4. Flint J, Kendler KS. The genetics of major depression. Neuron. 2014;81:484–503. https://linkinghub.elsevier.com/retrieve/pii/S0896-6273(14)00058-0.
5. Bastian F, Parmentier G, Roux J, Moretti S, Laudet V, Robinson-Rechavi M. Bgee: Integrating and comparing heterogeneous transcriptome data among species. In: International workshop on data integration in the life sciences. Springer; 2008. pp. 124–31. https://link.springer.com/chapter/10.1007/978-3-540-69828-9_12.
6. Komljenovic A R-RM Roux J, FB. B. BgeeDB, an r package for retrieval of curated expression datasets and for gene list expression localization enrichment tests [version 1; referees: 1 approved, 1 approved with reservations, 1 not approved]. F1000Research. 2016;5:2748. https://f1000research.com/articles/5-2748/v1.
7. Piñero J, Bravo À, Queralt-Rosinach N, Gutiérrez-Sacristán A, Deu-Pons J, Centeno E, et al. DisGeNET: A comprehensive platform integrating information on human disease-associated genes and variants. Nucleic Acids Research. 2016;gkw943. https://academic.oup.com/nar/article/45/D1/D833/2290909/DisGeNET-a-comprehensive-platform-integrating.