Difference between revisions of "Textpresso-based automated extraction of concise descriptions"

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==Generating gene sets with and without concise descriptions==
 
  
====Set of genes with a concise description====
 
Query for all genes with a concise description from Postgres:
 
Relevant postgres table names:
 
*con_wbgene: Stores the WBGene ID and gene names
 
*con_desctype: Type of description (relevant for us: Concise_description)
 
*con_desctext: Text of the concise description
 
 
Query for all WBGenes that have a concise description (in con_desctext AND con_desctype):
 
 
SELECT DISTINCT(con_wbgene) FROM con_wbgene WHERE joinkey IN (SELECT joinkey FROM con_desctext WHERE con_desctext IS NOT NULL) AND joinkey IN (SELECT joinkey FROM con_desctype WHERE con_desctype IS NOT NULL) ORDER BY con_wbgene;
 
 
*Number of genes with a concise description (as of 05.07.2014)=6,624
 
 
====Set of genes with no concise description====
 
====Set of genes with no concise description and at least one published paper====
 
 
==Location of project-related files on Textpresso==
 
http://textpresso-dev.caltech.edu/concise_descriptions/
 
 
 
==Semantic categories in a Concise Description==
 
1. Molecular identity <br \>
 
2. Orthology/Similarity <br \>
 
3. Mutant Phenotypes <br \>
 
4. Processes <br \>
 
5. Pathways <br \>
 
6. Genetic Interaction<br \>
 
7. Physical Interaction <br \>
 
8. Gene regulation data <br \>
 
9. Molecular Function <br \>
 
10. Tissue expression  (may include life-stage) <br \>
 
11. Sub-cellular localization  (may include life-stage) <br \>
 
 
==Data mining (mining data from Postgres and/or Acedb) for the semantic categories==
 
'''1. Molecular identity'''
 
*Caltech and non-caltech data?
 
*Source 1: GO data
 
**Download gene_association.wb.gz for C.elegans from GO consortium: http://www.geneontology.org/GO.current.annotations.shtml?all
 
**All rows with column 15 (assigned by) with 'WB' are WormBase annotations, those with 'UniProtKB' or 'InterPro' are from those databases
 
**Need data from these rows:
 
*** where column 9 has value 'F' (Molecular Function)
 
***column 2, associated genes, has UniProt ID or WormBase GeneID, need to translate UniProtID to WormBase ID.
 
***column 3: DB_Object symbol, eg, wht-7,
 
***column 5: GOID, eg, GO:0000346
 
***column 6: DB:Reference (Reference), eg.PMID:12062106, GO_REF:0000002
 
***column 7: Evidence code, eg, IMP
 
***column 15: Assigned By, eg., WB (which database created the annotation)
 
**For translation of UniProt IDs to WormBase Gene Ids use the file gp2protein.wb.gz at http://www.geneontology.org/gp2protein/
 
*Source 2: Homology data, see #2
 
 
'''2. Orthology, Homology and Paralog data'''
 
*Ace tags: ?Gene Ortholog_other, Paralog
 
*Contact: Michael Paulini
 
 
'''3. Processes'''
 
*Caltech data
 
*GO data
 
*Source 1: Download gene_association.wb.gz for C. elegans from GO consortium: http://www.geneontology.org/GO.current.annotations.shtml?all
 
**All rows with column 15 (assigned by) with 'WB' are WormBase annotations, those with 'UniProtKB' or 'InterPro' are from those databases
 
**Need data from these rows:
 
***where column 9: has value 'P' (Process),
 
***column 2 (DB_Object ID): the associated genes, UniProt ID or WBGene ID,
 
***column 3 (DB_Object symbol), eg, wht-7, GO terms are from column 5.
 
***column 5: GOID, eg, GO:0000346
 
***column 6: DB:Reference (Reference), eg.PMID:12062106, GO_REF:0000002
 
***column 7: Evidence code, eg, IMP
 
***column 8: With, eg. 'WB:WBRNAi00000785|WBPhenotype:0000050'
 
 
*GO data in postgres
 
**Paper -- gop_paper
 
**WBGene -- gop_wbgene
 
**GO -- gop_goontology
 
**GO Term -- gop_goid
 
*Contact Person: Kimberly, Ranjana
 
*Source 2: Topic data
 
**OA field: Gene, PG table name:pro_wbgene
 
**OA field:WBPaper, PG table name:pro_paper
 
*Contact Person: Karen
 
 
'''4. Pathway'''
 
(No database source for now?)
 
 
'''5. Mutant Phenotypes'''
 
*Caltech data
 
*Source 1: Phenotype OA, PG table name:(Phenotypes are added to variation and not genes)
 
*Source 2: Acedb tag: Under ?Gene, Reference_allele ?Variation and Allele ?Variation and Under ?Variation Phenotype
 
 
*Source 3: phenotype_association file:ftp://ftp.wormbase.org/pub/wormbase/releases/WS243/ONTOLOGY/
 
**File name:phenotype_association.WS243.wb
 
**Following rows:
 
***Rows with 'NOT' should be ignored for this search.
 
***column 2, associated genes, WormBase GeneID
 
***column 3: DB_Object symbol, eg, aap-1,
 
***column 5: Phenotype ID, eg, WBPhenotype:0000674
 
***column 6: DB:Reference (Reference), eg.WB_REF:WBPaper00032243, or WB:WBVar00249743
 
*Contact Person: Karen
 
 
'''6. Genetic Interaction and 7. Physical Interaction'''
 
*Caltech data
 
*Source 1: gene_association.wb
 
**ftp://ftp.wormbase.org/pub/wormbase/releases/WS243/ONTOLOGY/
 
**File name:gene_association.WS243.wb.c_elegans
 
**Rows with a 'IGI' in column 7 indicate a genetic interaction between the WBgenes in column 2/3 and column 8
 
**Rows with a 'IPI" in column 7 indicate a physical interaction between the WBgenes in column 2/3 and column 8
 
*Source 2: Interaction OA and tables
 
**"Field Name" = Postgres Table:
 
**"Paper" = int_paper
 
**"Interaction Type" = int_type
 
**"Bait overlapping gene" = int_genebait
 
**"Target overlapping gene" = int_genetarget
 
**"Non-directional Gene(s)" = int_genenondir
 
**"Effector Gene(s)" = int_geneone
 
**"Affected Gene(s)" = int_genetwo
 
 
Example statements:
 
 
If int_type = "Physical"
 
 
<int_genebait> interacts physically with <int_genetarget> (and vice versa)
 
 
 
If int_type = "Genetic - Synthetic ( Synthetic )"
 
 
<int_genenondir> interacts with <other int_genenondir(s)> in a synthetic
 
genetic interaction
 
 
 
If int_type = "Genetic - Suppression ( Suppression )"
 
 
<int_geneone> genetically suppresses <int_genetwo>
 
 
'''8. Gene regulation'''
 
*Caltech data
 
*Source: Gene regulation data in genereg OA
 
**Positive_regulate Anatomy_term "<grg_pos_anatomy>"
 
**Positive_regulate Life_stage "<grg_pos_lifestage>"
 
**Positive_regulate Subcellular_localization "<grg_pos_scl>"
 
**Positive_regulate Subcellular_localization_text "<grg_pos_scltext>"
 
**Negative_regulate Anatomy_term "<grg_neg_anatomy>"
 
**Negative_regulate Life_stage "<grg_neg_lifestage>"
 
**Negative_regulate Subcellular_localization "<grg_neg_scl>"
 
**Negative_regulate Subcellular_localization_text "<grg_neg_scltext>"
 
**Does_not_regulate Anatomy_term "<grg_not_anatomy>"
 
**Does_not_regulate Life_stage "<grg_not_lifestage>"
 
**Does_not_regulate Subcellular_localization "<grg_subcellloc>"
 
**Does_not_regulate Subcellular_localization_text "<grg_not_scltext>"
 
**Trans_regulated_gene "<grg_transregulated>"
 
**Trans_regulator_gene "<grg_transregulator>"
 
**No Subdata Result "<grg_result>"
 
 
'''9. Molecular Function'''
 
*Caltech data: GO Molecular Function
 
*Source 1: Download gene_association.wb.gz for C. elegans from GO consortium: http://www.geneontology.org/GO.current.annotations.shtml?all
 
**All rows with column 15 (assigned by) with 'WB' are WormBase annotations, those with 'UniProtKB' or 'InterPro' are from those databases
 
**Need data from these rows:
 
***where column 9: has value 'F' (Molecular Function),
 
***column 2 (DB_Object ID): the associated genes, UniProt ID or WBGene ID,
 
***column 3 (DB_Object symbol), eg, wht-7, GO terms are from column 5.
 
***column 5: GOID, eg, GO:0000346
 
***column 6: DB:Reference (Reference), eg.PMID:12062106, GO_REF:0000002
 
***column 7: Evidence code, eg, IDA
 
*Contact Person: Kimberly, Ranjana
 
 
'''10. Tissue expression and life stage'''
 
*Caltech data
 
*Source 1: Expression data
 
*OA (exprpat), PG table names:
 
**exp_anatomy for anatomy terms
 
**exp_goid for subcell localization
 
**exp_lifestage for life stage
 
**exp_paper for paper
 
**exp_gene for gene
 
*Contact Person: Daniela
 
 
'''11. Sub-cellular localization'''
 
*Caltech data
 
*GO data
 
*Source 1: gene_association file for C. elegans at:http://www.geneontology.org/GO.current.annotations.shtml?all
 
**Need data from these rows:
 
*** where column 9 has value 'C' (Cellular Component)
 
***column 2, associated genes, has UniProt ID or WormBase GeneID, need to translate UniProtID to WormBase ID.
 
***column 3: DB_Object symbol, eg, wht-7,
 
***column 5: GOID, eg, GO:0000346
 
***column 7: Evidence code, eg, IDA
 
 
Rule 1:
 
 
==Template for a Concise Description==
 
For the test phase, order of sentences:
 
*Orthology
 
*Process
 
*Component
 
*Function/identity
 
 
 
 
'''Orthology/Similarity'''
 
<Gene> is (orthologous, similar) to <human gene>;
 
'''Phenotypes'''
 
<Gene> mutants exhibit the following phenotypes: <phenotypes>.
 
'''Process/Pathway'''
 
<Gene> is (required, functions, regulates, is involved in, is part of) <process>;
 
'''Genetic interaction with respect to Process or Pathway'''
 
<Gene> interacts genetically with <gene1, gene2>;
 
'''Physical interaction'''
 
<Protein> physically interacts with (protein, DNA, RNA) .....;
 
'''Molecular Function'''
 
<Protein> has <molecular function>..... activity in (in vitro, in vivo);
 
'''Tissue Expression and sub-cellular localization'''
 
<Gene/Protein> is expressed in <tissue> and localized to <GO cellular component>;
 
 
Note: Not all descriptions may follow the exact order or choice of words.
 
 
==Rules for automated sentence construction==
 
'''Homology'''
 
 
<Gene> encodes an ortholog of human <human protein name>;
 
 
'''Process'''
 
*Rule 1: Ignore all IEA and ISS process terms
 
*Rule 2: Exclusions:
 
**Ignore the term 'reproduction'[IMP]
 
**Ignore the term 'embryo development ending in birth or egg hatching[IMP]'
 
*Rule 3: If a GO term has the words 'involved in' anywhere, beginning, middle or at the end, use the words 'functions in'
 
**Data: WBGene00006495,cpna-1,striated muscle contraction involved in embryonic body morphogenesis[IMP],WB_REF:WBPaper00041875|PMID:23283987
 
**Sentence: cpna-1 functions in striated muscle contraction involved in embryonic body morphogenesis;
 
*Rule 4: For the GO term 'synaptic transmission, <word>' switch the order of words to make it '<word> synaptic transmission'.
 
*Example for Rule 4:
 
**WBGene00011488,nra-2, synaptic transmission, cholinergic[IMP],WB_REF:WBPaper00034730|PMID:19609303,,WB,locomotion[IMP],protein processing[IEA],PMID:12520011|PMID:12654719,INTERPRO:IPR008710,regulation of signal transduction[IEA],INTERPRO:IPR016574
 
**nra-2 is involved in cholinergic synaptic transmission and locomotion.
 
 
*Rule 5: For all other Process terms the sentence will be:
 
**<Gene> is involved in <process term>;
 
**Examples:
 
**WBGene00014123,elpc-3,tRNA wobble uridine modification[IMP],WB_REF:WBPaper00034713|PMID:19593383,,WB,translation[IMP],spermatogenesis[IGI],olfactory learning[IMP],vulval development[IGI],embryonic morphogenesis[IGI],oocyte development[IGI]
 
**Sentence: elpc-3 is involved in tRNA wobble uridine modification, translation, spermatogenesis, olfactory learning, vulval development and embryonic morphogenesis.
 
 
*Rule 6: For the term 'molting cycle, collagen and cuticulin-based cuticle' GO term, drop the comma and the words 'collagen and cuticulin-based cuticle'
 
**Example:
 
**WBGene00016643,vps-45,molting cycle, collagen and cuticulin-based cuticle[IMP],WB_REF:WBPaper00029049|PMID:17235359,,WB,vesicle docking involved in exocytosis[IEA],PMID:12520011|PMID:12654719,INTERPRO:IPR001619,vesicle-mediated transport[IEA]
 
**Sentence: vps-45 is involved in '''the''' molting cycle;
 
 
'''Molecular identity'''
 
*Rule 1: If the evidence code is 'IEA' and 'activity' term is present, add the words 'based on protein domain information' to the sentence:
 
**Sentence: <Gene> is predicted to have <activity term>, based on protein domain information.
 
*Rule 2: If Evidence code is non-IEA
 
*Rule 3: Exclusion list:
 
**Ignore the term 'protein binding'
 
 
**Sentence: Gene exhibits <activity term, binding term>, based on experimental evidence.
 
 
 
'''Component'''
 
*Rule 1: Ignore all IEA and ISS GO terms, use only non-IEA GO terms
 
**Sentence: <Gene> is localized to <component term>;
 
*Rule 2: For 'integral component of ....' terms add the words 'is an';
 
**Eg. for Rule 2: WBGene00006319,sup-10,integral component of plasma membrane[IDA],WB_REF:WBPaper00006135|PMID:14534247,,WB,striated muscle dense body[IDA]
 
**sup-10 is an integral component of plasma membrane and is localized to striated muscle dense body;
 
*Examples
 
**WBGene00023405,sor-1,nucleoplasm[IDA],WB_REF:WBPaper00027128|PMID:16501168,,WB,nuclear speck[IDA]
 
**Sentence: sor-1 is localized to the nucleoplasm and nuclear speck;
 
 
**WBGene00004681,rsd-2,nucleolus[IDA],WB_REF:WBPaper00044261|PMID:18430922,,WB,endoplasmic reticulum[IDA],cytosol[IDA]
 
**Sentence: rsd-2 is localized to the nucleolus, endoplasmic reticulum and cytosol;
 
 
**WBGene00021827,dnc-6,dynactin complex[IDA],WB_REF:WBPaper00037699|PMID:20964796,,WB
 
**Sentence: dnc-6 is localized to the dynactin complex;
 
 
==Publications related to Text-mining methods==
 
*Automatically generating gene summaries from biomedical literature.
 
 
Ling X, Jiang J, He X, Mei Q, Zhai C, Schatz B.
 
 
Pac Symp Biocomput. 2006:40-51.
 
 
PMID:17094226
 
 
*Generating gene summaries from biomedical literature: A study of semi-structured summarization
 
 
Xu Ling *, Jing Jiang, Xin He, Qiaozhu Mei, Chengxiang Zhai, Bruce Schatz
 
 
Information Processing and Management 43 (2007) 1777–1791
 
 
 
Back To [[Concise Descriptions]]
 

Latest revision as of 23:01, 10 September 2014