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Gene Set Enrichment Analysis Report

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33 views3 pages

Gene Set Enrichment Analysis Report

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Raven Rousseau
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© © All Rights Reserved
We take content rights seriously. If you suspect this is your content, claim it here.
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Random Information Report: Gene set enrichment analysis

Name: Matthew Huang


Address: Unit 2611 Box 5936, DPO AE 85523
Email: [email protected]
Phone: +1-885-668-9215x3291
Company: Lee and Sons
Job: Cytogeneticist

{{Short description|Bioinformatics method}}


{{cs1 config|name-list-style=vanc|display-authors=6}}
[[File:Gsea meta.png|thumb|right|500 px|Schematic overview of the modular structure underlying procedures for gene set e

'''Gene set enrichment analysis (GSEA)''' (also called '''functional enrichment analysis''' or '''pathway enrichment analysis''')

Researchers performing [[high-throughput screening|high-throughput experiments]] that yield sets of genes (for example, g

== Background ==
After the completion of the [[Human Genome Project]], the problem of how to interpret and analyze it remained. In order to

== Methods ==
Gene set enrichment analysis uses ''[[A priori and a posteriori|a priori]]'' gene sets that have been grouped together by their

In the method that is typically referred to as standard GSEA, there are three steps involved in the analytical process.<ref na

# Calculate the ''enrichment score'' (ES) that represents the amount to which the genes in the set are over-represented at e
# Estimate the statistical significance of the ES. This calculation is done by a phenotypic-based permutation test in order to
#*Calculating significance this way tests for the dependence of the gene set on the diagnostic/phenotypic labels<ref name=
# Adjust for multiple hypothesis testing for when a large number of gene sets are being analyzed at one time. The enrichme
This can be described as:

<math display="block">
\begin{alignat}{1}
& P_{hit}(S, i)= \sum_{g_j \in S, j \leq i}\dfrac{|r_j|^p}{N_R}; \\[0.6ex]

& P_{miss}(S, i) = \sum_{g_j \not \in S, j \leq i}\dfrac{1}{N - N_H}; \\[0.6ex]

& N_R = \sum_{g_j \in S}|r_j|^p; \\[0.6ex]

& ES=P(S, i)=P_{hit}(S, i)-P_{miss}(S,i)=max(|P_{hit}(S, i)-P_{miss}(S, i)|) \\[0.6ex]


\end{alignat}
</math>
Where <math>r</math> is the rank of the gene, <math>p</math> is the power usually set to 1 (if it were 0, it would be equ

=== Limitations and proposed alternatives ===

==== SEA ====


When GSEA was first proposed in 2003 some immediate concerns were raised regarding its methodology. These criticism

==== SGSE ====


One other limitation to Gene Set Enrichment Analysis is that the results are very dependent on the algorithm that clusters t

1. Calculating the association between principal components and gene sets.<ref name="Frost_2015" />

2. Using the weighted Z-method to calculate the association between the gene sets and the spectral structure of the data
== Tools ==
GSEA uses complicated statistics, so it requires a computer program to run the calculations. GSEA ha

=== MOET===
Multi-Ontology Enrichment Tool (MOET) is a web-based ontology analysis tool that provides functiona

=== NASQAR ===


NASQAR (Nucleic Acid SeQuence Analysis Resource) is an open source, web-based platform for high

=== PlantRegMap===
The [[gene ontology]] (GO) annotation for 165 plant species and GO enrichment analysis is available.<

=== MSigDB ===


The Molecular Signatures Database hosts an extensive collection of annotated gene sets that can be u

=== Broad Institute ===


The [[Broad Institute]] website is in cooperation with MSigDB and has a downloadable GSEA software

=== WebGestalt ===


WebGestalt <ref>{{cite web|title=WebGestalt (WEB-based GEne SeT AnaLysis Toolkit)|url=http://www

=== Enrichr ===


Enrichr<ref>{{cite journal | vauthors = Chen EY, Tan CM, Kou Y, Duan Q, Wang Z, Meirelles GV, Clark

=== GeneSCF ===


GeneSCF is a real-time based functional enrichment tool with support for multiple organisms<ref name

=== DAVID ===


[[DAVID]] is the database for annotation, visualization and integrated discovery, a [[bioinformatics]] too

=== Metascape ===


[[Metascape]] is a biologist-oriented gene-list analysis portal.<ref>{{cite journal | vauthors = Zhou Y, Zh

===AmiGO 2===
The [[Gene Ontology]] (GO) consortium has also developed their own online GO term enrichment tool,
allowing species-specific enrichment analysis versus the complete database, coarser-grained GO slim

===GREAT===
Genomic region enrichment of annotations tool (GREAT) is a software which takes advantage of ''regu

=== FunRich ===


The Functional Enrichment Analysis (FunRich) tool<ref>{{cite web|title=FunRich :: Download|url=http:/

=== FuncAssociate ===


The FuncAssociate tool enables Gene Ontology and custom enrichment analyses.<ref name="Berriz_

=== InterMine ===


Instances of [[InterMine]] automatically provide enrichment analysis <ref>{{Cite web | url=https://interm

=== ToppGene suite ===


ToppGene is a one-stop portal for gene list enrichment analysis and candidate gene prioritization base

=== QuSAGE ===


Quantitative Set Analysis for Gene Expression (QuSAGE)] is a computational method for gene set enr
<ref>{{cite web | vauthors = Bolen C, Yaari G, Thakar J, Meng H, Turner J, Blankenship D, Kleinstein S

=== Blast2GO ===


Blast2GO is a bioinformatics platform for functional annotation and analysis of genomic datasets.<ref>

=== g:Profiler ===


g:Profiler is a toolset for finding biological categories enriched in gene lists, conversions between gene

== Applications ==

=== Genome-wide association studies ===


[[Single-nucleotide polymorphism]]s, or SNPs, are single base mutations that may be associated with d

=== Spontaneous preterm birth ===


Gene set enrichment methods led to the discovery of new suspect genes and biological pathways rela

=== Cancer cell profiling ===


Gene set enrichment analysis can be used to understand the changes that cells undergo during [[carci

=== Schizophrenia ===


GSEA can be used to help understand the molecular mechanisms of complex disorders. Schizophreni

=== Depression ===


GSEA can help provide molecular evidence for the association of biological pathways with diseases. P

== See also ==
*[[Gene Ontology Term Enrichment]]

== References ==
{{Reflist}}

== Further reading ==
{{refbegin}}
* {{cite journal | vauthors = Subramanian A, Tamayo P, Mootha VK, Mukherjee S, Ebert BL, Gillette MA
* {{cite journal | vauthors = Reimand J, Isserlin R, Voisin V, Kucera M, Tannus-Lopes C, Rostamianfar
* {{cite journal | vauthors = Chicco D, Agapito G | title = Nine quick tips for pathway enrichment analysi
{{refend}}

== External links ==
*[https://www.gsea-msigdb.org/gsea/msigdb/ Molecular Signatures Database (MSigDB)]
{{Bioinformatics}}
{{Portal bar|Biology|Medicine}}

[[Category:Proteomics| ]]
[[Category:Genomics]]
[[Category:Bioinformatics]]
[[Category:Microarrays]]

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