Cargando…
Literature Lab: a method of automated literature interrogation to infer biology from microarray analysis
BACKGROUND: The biomedical literature is a rich source of associative information but too vast for complete manual review. We have developed an automated method of literature interrogation called "Literature Lab" that identifies and ranks associations existing in the literature between gen...
Autores principales: | , , , , , , , |
---|---|
Formato: | Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2007
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2244637/ https://www.ncbi.nlm.nih.gov/pubmed/18088408 http://dx.doi.org/10.1186/1471-2164-8-461 |
_version_ | 1782150649277841408 |
---|---|
author | Febbo, Phillip G Mulligan, Mike G Slonina, David A Stegmeir, Kimberly Di Vizio, Dolores Martinez, Paul R Loda, Massimo Taylor, Stephen C |
author_facet | Febbo, Phillip G Mulligan, Mike G Slonina, David A Stegmeir, Kimberly Di Vizio, Dolores Martinez, Paul R Loda, Massimo Taylor, Stephen C |
author_sort | Febbo, Phillip G |
collection | PubMed |
description | BACKGROUND: The biomedical literature is a rich source of associative information but too vast for complete manual review. We have developed an automated method of literature interrogation called "Literature Lab" that identifies and ranks associations existing in the literature between gene sets, such as those derived from microarray experiments, and curated sets of key terms (i.e. pathway names, medical subject heading (MeSH) terms, etc). RESULTS: Literature Lab was developed using differentially expressed gene sets from three previously published cancer experiments and tested on a fourth, novel gene set. When applied to the genesets from the published data including an in vitro experiment, an in vivo mouse experiment, and an experiment with human tumor samples, Literature Lab correctly identified known biological processes occurring within each experiment. When applied to a novel set of genes differentially expressed between locally invasive and metastatic prostate cancer, Literature Lab identified a strong association between the pathway term "FOSB" and genes with increased expression in metastatic prostate cancer. Immunohistochemistry subsequently confirmed increased nuclear FOSB staining in metastatic compared to locally invasive prostate cancers. CONCLUSION: This work demonstrates that Literature Lab can discover key biological processes by identifying meritorious associations between experimentally derived gene sets and key terms within the biomedical literature. |
format | Text |
id | pubmed-2244637 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2007 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-22446372008-02-15 Literature Lab: a method of automated literature interrogation to infer biology from microarray analysis Febbo, Phillip G Mulligan, Mike G Slonina, David A Stegmeir, Kimberly Di Vizio, Dolores Martinez, Paul R Loda, Massimo Taylor, Stephen C BMC Genomics Software BACKGROUND: The biomedical literature is a rich source of associative information but too vast for complete manual review. We have developed an automated method of literature interrogation called "Literature Lab" that identifies and ranks associations existing in the literature between gene sets, such as those derived from microarray experiments, and curated sets of key terms (i.e. pathway names, medical subject heading (MeSH) terms, etc). RESULTS: Literature Lab was developed using differentially expressed gene sets from three previously published cancer experiments and tested on a fourth, novel gene set. When applied to the genesets from the published data including an in vitro experiment, an in vivo mouse experiment, and an experiment with human tumor samples, Literature Lab correctly identified known biological processes occurring within each experiment. When applied to a novel set of genes differentially expressed between locally invasive and metastatic prostate cancer, Literature Lab identified a strong association between the pathway term "FOSB" and genes with increased expression in metastatic prostate cancer. Immunohistochemistry subsequently confirmed increased nuclear FOSB staining in metastatic compared to locally invasive prostate cancers. CONCLUSION: This work demonstrates that Literature Lab can discover key biological processes by identifying meritorious associations between experimentally derived gene sets and key terms within the biomedical literature. BioMed Central 2007-12-18 /pmc/articles/PMC2244637/ /pubmed/18088408 http://dx.doi.org/10.1186/1471-2164-8-461 Text en Copyright © 2007 Febbo et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Software Febbo, Phillip G Mulligan, Mike G Slonina, David A Stegmeir, Kimberly Di Vizio, Dolores Martinez, Paul R Loda, Massimo Taylor, Stephen C Literature Lab: a method of automated literature interrogation to infer biology from microarray analysis |
title | Literature Lab: a method of automated literature interrogation to infer biology from microarray analysis |
title_full | Literature Lab: a method of automated literature interrogation to infer biology from microarray analysis |
title_fullStr | Literature Lab: a method of automated literature interrogation to infer biology from microarray analysis |
title_full_unstemmed | Literature Lab: a method of automated literature interrogation to infer biology from microarray analysis |
title_short | Literature Lab: a method of automated literature interrogation to infer biology from microarray analysis |
title_sort | literature lab: a method of automated literature interrogation to infer biology from microarray analysis |
topic | Software |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2244637/ https://www.ncbi.nlm.nih.gov/pubmed/18088408 http://dx.doi.org/10.1186/1471-2164-8-461 |
work_keys_str_mv | AT febbophillipg literaturelabamethodofautomatedliteratureinterrogationtoinferbiologyfrommicroarrayanalysis AT mulliganmikeg literaturelabamethodofautomatedliteratureinterrogationtoinferbiologyfrommicroarrayanalysis AT sloninadavida literaturelabamethodofautomatedliteratureinterrogationtoinferbiologyfrommicroarrayanalysis AT stegmeirkimberly literaturelabamethodofautomatedliteratureinterrogationtoinferbiologyfrommicroarrayanalysis AT diviziodolores literaturelabamethodofautomatedliteratureinterrogationtoinferbiologyfrommicroarrayanalysis AT martinezpaulr literaturelabamethodofautomatedliteratureinterrogationtoinferbiologyfrommicroarrayanalysis AT lodamassimo literaturelabamethodofautomatedliteratureinterrogationtoinferbiologyfrommicroarrayanalysis AT taylorstephenc literaturelabamethodofautomatedliteratureinterrogationtoinferbiologyfrommicroarrayanalysis |