Identification of histone modifications in biomedical text for supporting epigenomic research

Background Posttranslational modifications of histones influence the structure of chromatine and in such a way take part in the regulation of gene expression. Certain histone modification patterns, distributed over the genome, are connected to cell as well as tissue differentiation and to the adapti...

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Published inBMC bioinformatics Vol. 10; no. Suppl 1; p. S28
Main Authors Kolářik, Corinna, Klinger, Roman, Hofmann-Apitius, Martin
Format Journal Article
LanguageEnglish
Published London BioMed Central 30.01.2009
BioMed Central Ltd
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ISSN1471-2105
1471-2105
DOI10.1186/1471-2105-10-S1-S28

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Abstract Background Posttranslational modifications of histones influence the structure of chromatine and in such a way take part in the regulation of gene expression. Certain histone modification patterns, distributed over the genome, are connected to cell as well as tissue differentiation and to the adaption of organisms to their environment. Abnormal changes instead influence the development of disease states like cancer. The regulation mechanisms for modifying histones and its functionalities are the subject of epigenomics investigation and are still not completely understood. Text provides a rich resource of knowledge on epigenomics and modifications of histones in particular. It contains information about experimental studies, the conditions used, and results. To our knowledge, no approach has been published so far for identifying histone modifications in text. Results We have developed an approach for identifying histone modifications in biomedical literature with Conditional Random Fields (CRF) and for resolving the recognized histone modification term variants by term standardization. For the term identification F 1 measures of 0.84 by 10-fold cross-validation on the training corpus and 0.81 on an independent test corpus have been obtained. The standardization enabled the correct transformation of 96% of the terms from training and 98% from test the corpus. Due to the lack of terminologies exhaustively covering specific histone modification types, we developed a histone modification term hierarchy for use in a semantic text retrieval system. Conclusion The developed approach highly improves the retrieval of articles describing histone modifications. Since text contains context information about performed studies and experiments, the identification of histone modifications is the basis for supporting literature-based knowledge discovery and hypothesis generation to accelerate epigenomic research.
AbstractList Posttranslational modifications of histones influence the structure of chromatine and in such a way take part in the regulation of gene expression. Certain histone modification patterns, distributed over the genome, are connected to cell as well as tissue differentiation and to the adaption of organisms to their environment. Abnormal changes instead influence the development of disease states like cancer. The regulation mechanisms for modifying histones and its functionalities are the subject of epigenomics investigation and are still not completely understood. Text provides a rich resource of knowledge on epigenomics and modifications of histones in particular. It contains information about experimental studies, the conditions used, and results. To our knowledge, no approach has been published so far for identifying histone modifications in text. We have developed an approach for identifying histone modifications in biomedical literature with Conditional Random Fields (CRF) and for resolving the recognized histone modification term variants by term standardization. For the term identification F1 measures of 0.84 by 10-fold cross-validation on the training corpus and 0.81 on an independent test corpus have been obtained. The standardization enabled the correct transformation of 96% of the terms from training and 98% from test the corpus. Due to the lack of terminologies exhaustively covering specific histone modification types, we developed a histone modification term hierarchy for use in a semantic text retrieval system. The developed approach highly improves the retrieval of articles describing histone modifications. Since text contains context information about performed studies and experiments, the identification of histone modifications is the basis for supporting literature-based knowledge discovery and hypothesis generation to accelerate epigenomic research.
BACKGROUND: Posttranslational modifications of histones influence the structure of chromatine and in such a way take part in the regulation of gene expression. Certain histone modification patterns, distributed over the genome, are connected to cell as well as tissue differentiation and to the adaption of organisms to their environment. Abnormal changes instead influence the development of disease states like cancer. The regulation mechanisms for modifying histones and its functionalities are the subject of epigenomics investigation and are still not completely understood. Text provides a rich resource of knowledge on epigenomics and modifications of histones in particular. It contains information about experimental studies, the conditions used, and results. To our knowledge, no approach has been published so far for identifying histone modifications in text. RESULTS: We have developed an approach for identifying histone modifications in biomedical literature with Conditional Random Fields (CRF) and for resolving the recognized histone modification term variants by term standardization. For the term identification F1 measures of 0.84 by 10-fold cross-validation on the training corpus and 0.81 on an independent test corpus have been obtained. The standardization enabled the correct transformation of 96% of the terms from training and 98% from test the corpus. Due to the lack of terminologies exhaustively covering specific histone modification types, we developed a histone modification term hierarchy for use in a semantic text retrieval system. CONCLUSION: The developed approach highly improves the retrieval of articles describing histone modifications. Since text contains context information about performed studies and experiments, the identification of histone modifications is the basis for supporting literature-based knowledge discovery and hypothesis generation to accelerate epigenomic research.
Background Posttranslational modifications of histones influence the structure of chromatine and in such a way take part in the regulation of gene expression. Certain histone modification patterns, distributed over the genome, are connected to cell as well as tissue differentiation and to the adaption of organisms to their environment. Abnormal changes instead influence the development of disease states like cancer. The regulation mechanisms for modifying histones and its functionalities are the subject of epigenomics investigation and are still not completely understood. Text provides a rich resource of knowledge on epigenomics and modifications of histones in particular. It contains information about experimental studies, the conditions used, and results. To our knowledge, no approach has been published so far for identifying histone modifications in text. Results We have developed an approach for identifying histone modifications in biomedical literature with Conditional Random Fields (CRF) and for resolving the recognized histone modification term variants by term standardization. For the term identification F 1 measures of 0.84 by 10-fold cross-validation on the training corpus and 0.81 on an independent test corpus have been obtained. The standardization enabled the correct transformation of 96% of the terms from training and 98% from test the corpus. Due to the lack of terminologies exhaustively covering specific histone modification types, we developed a histone modification term hierarchy for use in a semantic text retrieval system. Conclusion The developed approach highly improves the retrieval of articles describing histone modifications. Since text contains context information about performed studies and experiments, the identification of histone modifications is the basis for supporting literature-based knowledge discovery and hypothesis generation to accelerate epigenomic research.
Posttranslational modifications of histones influence the structure of chromatine and in such a way take part in the regulation of gene expression. Certain histone modification patterns, distributed over the genome, are connected to cell as well as tissue differentiation and to the adaption of organisms to their environment. Abnormal changes instead influence the development of disease states like cancer. The regulation mechanisms for modifying histones and its functionalities are the subject of epigenomics investigation and are still not completely understood. Text provides a rich resource of knowledge on epigenomics and modifications of histones in particular. It contains information about experimental studies, the conditions used, and results. To our knowledge, no approach has been published so far for identifying histone modifications in text.BACKGROUNDPosttranslational modifications of histones influence the structure of chromatine and in such a way take part in the regulation of gene expression. Certain histone modification patterns, distributed over the genome, are connected to cell as well as tissue differentiation and to the adaption of organisms to their environment. Abnormal changes instead influence the development of disease states like cancer. The regulation mechanisms for modifying histones and its functionalities are the subject of epigenomics investigation and are still not completely understood. Text provides a rich resource of knowledge on epigenomics and modifications of histones in particular. It contains information about experimental studies, the conditions used, and results. To our knowledge, no approach has been published so far for identifying histone modifications in text.We have developed an approach for identifying histone modifications in biomedical literature with Conditional Random Fields (CRF) and for resolving the recognized histone modification term variants by term standardization. For the term identification F1 measures of 0.84 by 10-fold cross-validation on the training corpus and 0.81 on an independent test corpus have been obtained. The standardization enabled the correct transformation of 96% of the terms from training and 98% from test the corpus. Due to the lack of terminologies exhaustively covering specific histone modification types, we developed a histone modification term hierarchy for use in a semantic text retrieval system.RESULTSWe have developed an approach for identifying histone modifications in biomedical literature with Conditional Random Fields (CRF) and for resolving the recognized histone modification term variants by term standardization. For the term identification F1 measures of 0.84 by 10-fold cross-validation on the training corpus and 0.81 on an independent test corpus have been obtained. The standardization enabled the correct transformation of 96% of the terms from training and 98% from test the corpus. Due to the lack of terminologies exhaustively covering specific histone modification types, we developed a histone modification term hierarchy for use in a semantic text retrieval system.The developed approach highly improves the retrieval of articles describing histone modifications. Since text contains context information about performed studies and experiments, the identification of histone modifications is the basis for supporting literature-based knowledge discovery and hypothesis generation to accelerate epigenomic research.CONCLUSIONThe developed approach highly improves the retrieval of articles describing histone modifications. Since text contains context information about performed studies and experiments, the identification of histone modifications is the basis for supporting literature-based knowledge discovery and hypothesis generation to accelerate epigenomic research.
ArticleNumber S28
Author Kolářik, Corinna
Klinger, Roman
Hofmann-Apitius, Martin
AuthorAffiliation 1 Department of Bioinformatics, Fraunhofer Institute Algorithms and Scientific Computing (SCAI) Schloß Birlinghoven, D-53754 Sankt Augustin, Germany
2 Department of Applied Life Science Informatics, Bonn-Aachen International Center for Information Technology (B-IT) Dahlmannstrasse 2, D-53113 Bonn, Germany
AuthorAffiliation_xml – name: 2 Department of Applied Life Science Informatics, Bonn-Aachen International Center for Information Technology (B-IT) Dahlmannstrasse 2, D-53113 Bonn, Germany
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Cites_doi 10.1016/j.gde.2006.02.015
10.1038/nsmb1307
10.1142/S0219720007003156
10.1186/gb-2006-7-5-402
10.1016/j.cell.2006.07.026
10.1038/sj.ejhg.5201727
10.1093/bioinformatics/btm236
10.1093/bioinformatics/btm235
10.1016/j.gde.2005.01.005
10.1016/S0169-2607(98)00033-9
10.1038/nature05919
10.1093/bioinformatics/btn181
10.1093/bioinformatics/btm461
10.1002/prot.20814
10.1016/j.cell.2004.08.020
10.1038/nsmb1338
10.1093/toxsci/kfm177
10.1186/1471-2105-6-S1-S6
10.1186/1471-2105-6-S1-S14
10.1093/mutage/gel068
10.1126/science.1063127
10.1093/bioinformatics/18.8.1124
10.1093/nar/gkm788
10.1371/journal.pbio.0020309
10.1007/s11154-007-9042-4
10.1098/rsta.2008.0099
10.1038/nsmb0205-110
10.1016/j.ijmedinf.2004.04.024
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Issue Suppl 1
Keywords MeSH
Conditional Random Field
Histone Modification
Gene Ontology
Name Entity Recognition
Language English
License http://creativecommons.org/licenses/by/2.0
This is an open access article distributed under the terms of the Creative Commons Attribution License (), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
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References T Jenuwein (3211_CR3) 2001; 293
JG Caporaso (3211_CR18) 2007; 23
R Margueron (3211_CR1) 2005; 15
GL Cuthbert (3211_CR42) 2004; 118
CJ Nelson (3211_CR43) 2006; 126
LJG Post (3211_CR33) 2007; 23
L Tanabe (3211_CR16) 2002; 18
3211_CR20
3211_CR40
HM Müller (3211_CR34) 2004; 2
M Szyf (3211_CR4) 2007; 100
D Karolchik (3211_CR9) 2007
SD Taverna (3211_CR2) 2007; 14
R Klinger (3211_CR23) 2007; 5
BM Turner (3211_CR22) 2005; 12
AK McCallum (3211_CR28) 2002
T Morton (3211_CR29) 2003
L Marino-Ramírez (3211_CR11) 2006; 62
NR Smalheiser (3211_CR13) 1998; 57
KP Nightingale (3211_CR21) 2006; 16
R Klinger (3211_CR27) 2007
3211_CR32
AP Feinberg (3211_CR8) 2007; 447
J Tamames (3211_CR24) 2006; 7
CB Santos-Rebouças (3211_CR7) 2007; 15
3211_CR30
3211_CR31
M Ongenaert (3211_CR19) 2008; 36
R Klinger (3211_CR15) 2008; 24
D Hristovski (3211_CR14) 2005; 74
R McDonald (3211_CR26) 2005; 6
3211_CR38
3211_CR39
3211_CR36
JD Lafferty (3211_CR25) 2001
3211_CR37
3211_CR12
W yee Tang (3211_CR5) 2007; 8
JA Latham (3211_CR41) 2007; 14
D Hanisch (3211_CR17) 2005; 6
Z Herceg (3211_CR6) 2007; 22
TR O'Connor (3211_CR10) 2007; 23
M Hofmann-Apitius (3211_CR35) 2008; 366
15702071 - Nat Struct Mol Biol. 2005 Feb;12(2):110-2
11498575 - Science. 2001 Aug 10;293(5532):1074-80
15694635 - Int J Med Inform. 2005 Mar;74(2-4):289-98
15339660 - Cell. 2004 Sep 3;118(5):545-53
16503131 - Curr Opin Genet Dev. 2006 Apr;16(2):125-36
17984964 - Nat Struct Mol Biol. 2007 Nov;14(11):1017-24
17284773 - Mutagenesis. 2007 Mar;22(2):91-103
16959570 - Cell. 2006 Sep 8;126(5):905-16
17932060 - Nucleic Acids Res. 2008 Jan;36(Database issue):D842-6
18586724 - Bioinformatics. 2008 Jul 1;24(13):i268-76
16707004 - Genome Biol. 2006;7(5):402
15960826 - BMC Bioinformatics. 2005;6 Suppl 1:S14
17638084 - Rev Endocr Metab Disord. 2007 Jun;8(2):173-82
15797199 - Curr Opin Genet Dev. 2005 Apr;15(2):163-76
16345076 - Proteins. 2006 Mar 1;62(4):838-42
17522677 - Nature. 2007 May 24;447(7143):433-40
9822851 - Comput Methods Programs Biomed. 1998 Nov;57(3):149-53
15960840 - BMC Bioinformatics. 2005;6 Suppl 1:S6
18172929 - J Bioinform Comput Biol. 2007 Dec;5(6):1277-96
17047674 - Eur J Hum Genet. 2007 Jan;15(1):10-7
17485428 - Bioinformatics. 2007 Jul 15;23(14):1828-30
17495998 - Bioinformatics. 2007 Jul 15;23(14):1862-5
12176836 - Bioinformatics. 2002 Aug;18(8):1124-32
15383839 - PLoS Biol. 2004 Nov;2(11):e309
17675334 - Toxicol Sci. 2007 Nov;100(1):7-23
17984965 - Nat Struct Mol Biol. 2007 Nov;14(11):1025-40
17881406 - Bioinformatics. 2007 Nov 15;23(22):3080-7
18559317 - Philos Trans A Math Phys Eng Sci. 2008 Sep 13;366(1878):3091-110
18428780 - Curr Protoc Bioinformatics. 2007 Mar;Chapter 1:Unit 1.4
References_xml – ident: 3211_CR36
– volume: 16
  start-page: 125
  issue: 2
  year: 2006
  ident: 3211_CR21
  publication-title: Curr Opin Genet Dev
  doi: 10.1016/j.gde.2006.02.015
– ident: 3211_CR38
– volume-title: Curr Protoc Bioinformatics
  year: 2007
  ident: 3211_CR9
– ident: 3211_CR32
– ident: 3211_CR40
– volume: 14
  start-page: 1017
  issue: 11
  year: 2007
  ident: 3211_CR41
  publication-title: Nat Struct Mol Biol
  doi: 10.1038/nsmb1307
– start-page: 282
  volume-title: Proceedings of the Eighteenth International Conference on Machine Learning
  year: 2001
  ident: 3211_CR25
– volume: 5
  start-page: 1277
  issue: 6
  year: 2007
  ident: 3211_CR23
  publication-title: Journal of Bioinformatics and Computational Biology
  doi: 10.1142/S0219720007003156
– volume: 7
  start-page: 402
  issue: 5
  year: 2006
  ident: 3211_CR24
  publication-title: Genome Biol
  doi: 10.1186/gb-2006-7-5-402
– volume: 126
  start-page: 905
  issue: 5
  year: 2006
  ident: 3211_CR43
  publication-title: Cell
  doi: 10.1016/j.cell.2006.07.026
– volume: 15
  start-page: 10
  year: 2007
  ident: 3211_CR7
  publication-title: Eur J Hum Genet
  doi: 10.1038/sj.ejhg.5201727
– volume: 23
  start-page: 1828
  issue: 14
  year: 2007
  ident: 3211_CR10
  publication-title: Bioinformatics
  doi: 10.1093/bioinformatics/btm236
– volume: 23
  start-page: 1862
  issue: 14
  year: 2007
  ident: 3211_CR18
  publication-title: Bioinformatics
  doi: 10.1093/bioinformatics/btm235
– volume: 15
  start-page: 163
  issue: 2
  year: 2005
  ident: 3211_CR1
  publication-title: Curr Opin Genet Dev
  doi: 10.1016/j.gde.2005.01.005
– volume: 57
  start-page: 149
  issue: 3
  year: 1998
  ident: 3211_CR13
  publication-title: Comput Methods Programs Biomed
  doi: 10.1016/S0169-2607(98)00033-9
– volume: 447
  start-page: 433
  issue: 7143
  year: 2007
  ident: 3211_CR8
  publication-title: Nature
  doi: 10.1038/nature05919
– ident: 3211_CR31
– volume: 24
  start-page: i268
  issue: 13
  year: 2008
  ident: 3211_CR15
  publication-title: Bioinformatics
  doi: 10.1093/bioinformatics/btn181
– volume: 23
  start-page: 3080
  issue: 22
  year: 2007
  ident: 3211_CR33
  publication-title: Bioinformatics
  doi: 10.1093/bioinformatics/btm461
– volume: 62
  start-page: 838
  issue: 4
  year: 2006
  ident: 3211_CR11
  publication-title: Proteins
  doi: 10.1002/prot.20814
– volume: 118
  start-page: 545
  issue: 5
  year: 2004
  ident: 3211_CR42
  publication-title: Cell
  doi: 10.1016/j.cell.2004.08.020
– volume: 14
  start-page: 1025
  issue: 11
  year: 2007
  ident: 3211_CR2
  publication-title: Nat Struct Mol Biol
  doi: 10.1038/nsmb1338
– volume: 100
  start-page: 7
  year: 2007
  ident: 3211_CR4
  publication-title: Toxicol Sci
  doi: 10.1093/toxsci/kfm177
– volume: 6
  start-page: S6
  issue: Suppl 1
  year: 2005
  ident: 3211_CR26
  publication-title: BMC Bioinformatics
  doi: 10.1186/1471-2105-6-S1-S6
– ident: 3211_CR37
– ident: 3211_CR12
– volume: 6
  start-page: S14
  issue: Suppl 1
  year: 2005
  ident: 3211_CR17
  publication-title: BMC Bioinformatics
  doi: 10.1186/1471-2105-6-S1-S14
– volume: 22
  start-page: 91
  issue: 2
  year: 2007
  ident: 3211_CR6
  publication-title: Mutagenesis
  doi: 10.1093/mutage/gel068
– ident: 3211_CR39
– volume: 293
  start-page: 1074
  issue: 5532
  year: 2001
  ident: 3211_CR3
  publication-title: Science
  doi: 10.1126/science.1063127
– volume: 18
  start-page: 1124
  issue: 8
  year: 2002
  ident: 3211_CR16
  publication-title: Bioinformatics
  doi: 10.1093/bioinformatics/18.8.1124
– volume-title: MALLET: A Machine Learning for Language Toolkit
  year: 2002
  ident: 3211_CR28
– start-page: 17
  volume-title: HLT/NAACL 2003: demonstrations
  year: 2003
  ident: 3211_CR29
– volume: 36
  start-page: D842
  year: 2008
  ident: 3211_CR19
  publication-title: Nucleic Acids Res
  doi: 10.1093/nar/gkm788
– volume-title: Tech Rep TR07-2-013
  year: 2007
  ident: 3211_CR27
– ident: 3211_CR30
– ident: 3211_CR20
– volume: 2
  start-page: e309
  issue: 11
  year: 2004
  ident: 3211_CR34
  publication-title: PLoS Biol
  doi: 10.1371/journal.pbio.0020309
– volume: 8
  start-page: 173
  issue: 2
  year: 2007
  ident: 3211_CR5
  publication-title: Rev Endocr Metab Disord
  doi: 10.1007/s11154-007-9042-4
– volume: 366
  start-page: 3091
  issue: 1878
  year: 2008
  ident: 3211_CR35
  publication-title: Philosophical Transactions of the Royal Society A
  doi: 10.1098/rsta.2008.0099
– volume: 12
  start-page: 110
  issue: 2
  year: 2005
  ident: 3211_CR22
  publication-title: Nat Struct Mol Biol
  doi: 10.1038/nsmb0205-110
– volume: 74
  start-page: 289
  issue: 2–4
  year: 2005
  ident: 3211_CR14
  publication-title: Int J Med Inform
  doi: 10.1016/j.ijmedinf.2004.04.024
– reference: 15339660 - Cell. 2004 Sep 3;118(5):545-53
– reference: 17984964 - Nat Struct Mol Biol. 2007 Nov;14(11):1017-24
– reference: 16503131 - Curr Opin Genet Dev. 2006 Apr;16(2):125-36
– reference: 18428780 - Curr Protoc Bioinformatics. 2007 Mar;Chapter 1:Unit 1.4
– reference: 12176836 - Bioinformatics. 2002 Aug;18(8):1124-32
– reference: 17984965 - Nat Struct Mol Biol. 2007 Nov;14(11):1025-40
– reference: 15702071 - Nat Struct Mol Biol. 2005 Feb;12(2):110-2
– reference: 18172929 - J Bioinform Comput Biol. 2007 Dec;5(6):1277-96
– reference: 18559317 - Philos Trans A Math Phys Eng Sci. 2008 Sep 13;366(1878):3091-110
– reference: 16707004 - Genome Biol. 2006;7(5):402
– reference: 17638084 - Rev Endocr Metab Disord. 2007 Jun;8(2):173-82
– reference: 17932060 - Nucleic Acids Res. 2008 Jan;36(Database issue):D842-6
– reference: 18586724 - Bioinformatics. 2008 Jul 1;24(13):i268-76
– reference: 15383839 - PLoS Biol. 2004 Nov;2(11):e309
– reference: 17495998 - Bioinformatics. 2007 Jul 15;23(14):1862-5
– reference: 11498575 - Science. 2001 Aug 10;293(5532):1074-80
– reference: 15694635 - Int J Med Inform. 2005 Mar;74(2-4):289-98
– reference: 15797199 - Curr Opin Genet Dev. 2005 Apr;15(2):163-76
– reference: 16345076 - Proteins. 2006 Mar 1;62(4):838-42
– reference: 15960826 - BMC Bioinformatics. 2005;6 Suppl 1:S14
– reference: 17485428 - Bioinformatics. 2007 Jul 15;23(14):1828-30
– reference: 17881406 - Bioinformatics. 2007 Nov 15;23(22):3080-7
– reference: 15960840 - BMC Bioinformatics. 2005;6 Suppl 1:S6
– reference: 16959570 - Cell. 2006 Sep 8;126(5):905-16
– reference: 9822851 - Comput Methods Programs Biomed. 1998 Nov;57(3):149-53
– reference: 17284773 - Mutagenesis. 2007 Mar;22(2):91-103
– reference: 17522677 - Nature. 2007 May 24;447(7143):433-40
– reference: 17047674 - Eur J Hum Genet. 2007 Jan;15(1):10-7
– reference: 17675334 - Toxicol Sci. 2007 Nov;100(1):7-23
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Snippet Background Posttranslational modifications of histones influence the structure of chromatine and in such a way take part in the regulation of gene expression....
Posttranslational modifications of histones influence the structure of chromatine and in such a way take part in the regulation of gene expression. Certain...
BACKGROUND: Posttranslational modifications of histones influence the structure of chromatine and in such a way take part in the regulation of gene expression....
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SubjectTerms Algorithms
Bioinformatics
Biomedical and Life Sciences
Computational Biology/Bioinformatics
Computer Appl. in Life Sciences
Epigenesis, Genetic
Genome
Genomics - methods
Histones - chemistry
Histones - genetics
Histones - metabolism
Information Storage and Retrieval - methods
Life Sciences
Microarrays
Protein Processing, Post-Translational - genetics
Terminology as Topic
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Title Identification of histone modifications in biomedical text for supporting epigenomic research
URI https://link.springer.com/article/10.1186/1471-2105-10-S1-S28
https://www.ncbi.nlm.nih.gov/pubmed/19208128
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http://dx.doi.org/10.1186/1471-2105-10-S1-S28
https://pubmed.ncbi.nlm.nih.gov/PMC2648793
Volume 10
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