Semantic Web Approaches to Candidate Gene Identification
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Slides from my presentation at CSHALS 2010, Boston, February 25th 2010.
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Semantic Web Approaches to Candidate Gene Identification
- 1. Semantic Web Approaches to Candidate Gene Identification Simon Twigger, Ph.D.
- 4. Hypertensive
- 5. Hypertensive Hypertension
- 6. QTL Hypertensive Hypertension
- 7. QTL Hypertensive G G G Hypertension
- 8. QTL Hypertensive G G G Hypertension
- 9. QTL Hypertensive G G G Hypertension
- 11. Rat researchers ask... Has anyone done any expression studies using congenic rats?
- 12. Rat researchers ask... Has anyone done any expression studies using congenic rats? What tissue is this gene expressed in?
- 13. Rat researchers ask... Has anyone done any expression studies using congenic rats? What tissue is this gene expressed in? Are any of these genes associated with my phenotype?
- 14. Rat researchers ask... Has anyone done any expression studies using congenic rats? What tissue is this gene expressed in? Are any of these genes associated with my phenotype? What rat expression studies have been done on Mammary Cancer(aka breast neoplasms/breast cancer/cancer of the
- 15. Rat researchers ask... Has anyone done any expression studies using congenic rats? What tissue is this gene What expression data expressed in? is known for SD (aka Are any of these SD/NHsd, Harlan genes associated Sprague Dawley, with my phenotype? Sprague Dawley) rats? What rat expression studies have been done on Mammary Cancer(aka breast neoplasms/breast cancer/cancer of the
- 16. Rat researchers ask... Has anyone done any expression studies using congenic rats? What tissue is this gene What expression data expressed in? is known for SD (aka Are any of these SD/NHsd, Harlan genes associated Sprague Dawley, with my phenotype? Sprague Dawley) rats? Has this gene been seen in the brain? What rat expression studies have been done on Mammary Cancer(aka breast neoplasms/breast cancer/cancer of the
- 18. Biological Data Warehouse Really important piece of data...
- 19. NCBI GEO db
- 20. Data hidden in plain sight
- 22. Parallel Annotation Workflow GEO Records Create Annotation Jobs & Queue Up Q-Out 1..n Annot. Workers RabbitMQ Index text at OBA Parse Q-In Results Results saved to Put results in to GMiner database queue for save
- 23. Ontologies
- 24. gminer.mcw.edu
- 28. Addition of new annotations NCBO Ontology Widgets http://www.bioontology.org/wiki/index.php/Ontology_Widgets
- 29. Addition of new annotations NCBO Ontology Widgets http://www.bioontology.org/wiki/index.php/Ontology_Widgets
- 30. Addition of new annotations NCBO Ontology Widgets http://www.bioontology.org/wiki/index.php/Ontology_Widgets
- 31. Addition of new annotations NCBO Ontology Widgets http://www.bioontology.org/wiki/index.php/Ontology_Widgets
- 35. Linking annotations to data
- 36. Linking annotations to data
- 37. Linking annotations to data Tm2d1 RGD1306410 Svs4 Hbb Scgb2a1 Alb
- 38. Linking annotations to data Tm2d1 RGD1306410 Svs4 Hbb Scgb2a1 Alb
- 39. Linking annotations to data Tm2d1 RGD1306410 Svs4 Hbb Scgb2a1 + Alb
- 40. Linking annotations to data Tm2d1 RGD1306410 Svs4 Hbb Scgb2a1 + Alb Hbb is_expressed_in rat kidney Tm2d1 is_expressed_in rat kidney
- 41. Linking annotations to data Tm2d1 RGD1306410 Svs4 Hbb Scgb2a1 + Alb Hbb is_expressed_in rat kidney Tm2d1 is_expressed_in rat kidney Human (U133, U133v2.), Mouse (430, U74, U95) and Rat (U34a/b/c, 230, 230v2) 62,000 samples x ca. 25,000 genes/sample = 1.5B data points
- 42. Probeset results on GMiner Probeset 1395269_s_at for Gabrd - gamma-aminobutyric acid (GABA) A receptor, delta
- 43. Probeset results on GMiner Gabdr
- 44. Probeset results on GMiner Gabdr Hs GABDR
- 45. RDF Data integration Probeset to MA Triple Store
- 46. RDF Data integration Probeset Rat Genes to MA & xrefs Triple Store
- 47. RDF Data integration Probeset Rat Genes Probeset to to MA & xrefs RGD ID Triple Store
- 48. RDF Data integration Probeset Rat Genes Probeset to Mouse Anatomy to MA & xrefs RGD ID Ontology Triple Store
- 49. RDF Data integration Probeset Rat Genes Probeset to Mouse Anatomy to MA & xrefs RGD ID Ontology Triple Store
- 50. QTL Hypertensive G G G Hypertension
- 51. QTL Hypertensive G G G Hypertension
- 52. QTL Hypertensive G G G Pathway Hypertension
- 53. QTL Hypertensive G G G Pathway G G Hypertension
- 54. QTL Hypertensive G G G Pathway G G Component Function Process Hypertension
- 55. QTL Hypertensive G G G Pathway G G Component Function Process Hypertension
- 56. QTL Hypertensive G G G Pathway G G Anatomy (Kidney) Component Function Process Hypertension
- 57. QTL Hypertensive G G G Pathway Str 1 != Str 2 G G Anatomy (Kidney) Component Function Process Hypertension
- 58. Ongoing • Work on improving term recognition • Additional ontologies - Cell Type, Drugs, Phenotype, Disease • RDFizing (what URIs to use?) • Triple Store implementation • Integrate Strain and tissue results into RGD
- 59. Acknowledgements • Joey Geiger - Development of GMiner • Jennifer Smith - Video creation, data curation • Rajni Nigam - Rat Strain Ontology • Clement Jonquet - NCBO Annotator tools • Mark Musen & NIH Roadmap Initiative - Our Funding!
- 60. Links • http://gminer.mcw.edu Web application • http://github.com/mcwbbc/gminer Gminer Code • http://github.com/simont/MCW-RDF RDFizer code Email: simont@mcw.edu Twitter: @simon_t
Notas do Editor
- The Rat Genome Database is one of the main projects we have at MCW. It is the model organism database for the laboratory rat, Rattus norvegicus. We curate, genes, strains, QTL, etc. and make extensive use of ontologies such as GO, pathway, rat strain, disease, phenotype.
- This is a typical use case for rat genomics - how to identify the causes of hypertension in a hypertensive rat? Quite often a QTL is measured indicating a region on the chromosome that is statistically shown to be related to the trait in question - how to go from the genes in that region to the cause of the disease? Not an easy task - ‘then a miracle happens’
- This is a typical use case for rat genomics - how to identify the causes of hypertension in a hypertensive rat? Quite often a QTL is measured indicating a region on the chromosome that is statistically shown to be related to the trait in question - how to go from the genes in that region to the cause of the disease? Not an easy task - ‘then a miracle happens’
- This is a typical use case for rat genomics - how to identify the causes of hypertension in a hypertensive rat? Quite often a QTL is measured indicating a region on the chromosome that is statistically shown to be related to the trait in question - how to go from the genes in that region to the cause of the disease? Not an easy task - ‘then a miracle happens’
- This is a typical use case for rat genomics - how to identify the causes of hypertension in a hypertensive rat? Quite often a QTL is measured indicating a region on the chromosome that is statistically shown to be related to the trait in question - how to go from the genes in that region to the cause of the disease? Not an easy task - ‘then a miracle happens’
- This is a typical use case for rat genomics - how to identify the causes of hypertension in a hypertensive rat? Quite often a QTL is measured indicating a region on the chromosome that is statistically shown to be related to the trait in question - how to go from the genes in that region to the cause of the disease? Not an easy task - ‘then a miracle happens’
- Rat biologists ask many questions related to gene expression and diseases, these are some examples of typical questions. Many of these questions are in areas covered by ontologies and would benefit from the additional searching flexibility that ontologies provide
- Rat biologists ask many questions related to gene expression and diseases, these are some examples of typical questions. Many of these questions are in areas covered by ontologies and would benefit from the additional searching flexibility that ontologies provide
- Rat biologists ask many questions related to gene expression and diseases, these are some examples of typical questions. Many of these questions are in areas covered by ontologies and would benefit from the additional searching flexibility that ontologies provide
- Rat biologists ask many questions related to gene expression and diseases, these are some examples of typical questions. Many of these questions are in areas covered by ontologies and would benefit from the additional searching flexibility that ontologies provide
- Rat biologists ask many questions related to gene expression and diseases, these are some examples of typical questions. Many of these questions are in areas covered by ontologies and would benefit from the additional searching flexibility that ontologies provide
- Rat biologists ask many questions related to gene expression and diseases, these are some examples of typical questions. Many of these questions are in areas covered by ontologies and would benefit from the additional searching flexibility that ontologies provide
- Technical problem - lots of data being stored, hard to find it again. Government Warehouse image. Data is archived with good intentions but in doing so is often not easy to find again... If you cant find the data, its not really much use.
- NCBI’s Gene Expression Omnibus has a lot of relevant data, either as text or raw data.
- Can we start to capture some of this informaiton in an informatically-tractable fashion using ontologies and the OBA tools at the National Center for Biomedical Ontology in an annotation pipeline? The red boxes highlight some concepts of interest - rat strains and tissues being used in this experiment. A human can read these and know whats going on but what about a computer?
- Driving biological project - use NCBO Annotator web services to mark up the text in the GEO records using ontologies
- Take sections of text from GEO records, create annotation jobs, place in queue Workers take the jobs off the queue, index for appropriate ontologies at NCBO Results are placed on Input queue for saving back to the database.
- We are currently using two ontologies, the rat strain ontology created at RGD and the Mouse Gross Anatomy Ontology created at the JAX
- GEO data is run through the pipeline and loaded into Gminer for curation and analysis
- Annotated results can be reviewed and verified, some annotations are missed such as the Sprague Dawley link
- Annotated results can be reviewed and verified, some annotations are missed such as the Sprague Dawley link
- New annotations can be added using the NCBO ontology widgets
- New annotations can be added using the NCBO ontology widgets
- New annotations can be added using the NCBO ontology widgets
- Put the OBA system on an Amazon AMI so it can be instantiated at will Allows users to run as many of these things as they want? Consider using a Virtual Machine?
- Initial results focusing on GEO rat datasets has provided a lot of great information and allowed us to create some handy navigational interfaces to the data, enabling queries that were not possible on any other site. Want to find expression data for the SS rat Kidney - click the terms and the datasets appear.
- Initial results focusing on GEO rat datasets has provided a lot of great information and allowed us to create some handy navigational interfaces to the data, enabling queries that were not possible on any other site. Want to find expression data for the SS rat Kidney - click the terms and the datasets appear.
- Can we link from the annotations to the samples, down to the raw data in that sample and from there to the genes involved? Affy chips have the detection call, a fairly conservative present/absent call indicating if the probe set was observed in that particular sample.
- Can we link from the annotations to the samples, down to the raw data in that sample and from there to the genes involved? Affy chips have the detection call, a fairly conservative present/absent call indicating if the probe set was observed in that particular sample.
- Can we link from the annotations to the samples, down to the raw data in that sample and from there to the genes involved? Affy chips have the detection call, a fairly conservative present/absent call indicating if the probe set was observed in that particular sample.
- We can then related the probesets to the genes to the ontology annotations to create triple such as this. If we do this for the affy data in GEO for Rat, Mouse and Human we will have somewhere upwards of 1.5B data points to encode.
- We can then related the probesets to the genes to the ontology annotations to create triple such as this. If we do this for the affy data in GEO for Rat, Mouse and Human we will have somewhere upwards of 1.5B data points to encode.
- For each probe we can look at the samples in which it was tested and see if it was present/absent/marginal and compile this data to get a feel for how often a gene was seen in a particular tissue/organ.
- This can be viewed as a chart of tissue distribution. When compared to similar results from GeneCards/Novartis BioGPS the results are quite comparable indicating that this approach has some merit.
- Experimenting with exporting this data into RDF and integrating with related data and vocabularies in triple stores such as Sesame, AllegroGraph and Virtuoso. Early days, still climbing the learning curve with this!
- Experimenting with exporting this data into RDF and integrating with related data and vocabularies in triple stores such as Sesame, AllegroGraph and Virtuoso. Early days, still climbing the learning curve with this!
- Experimenting with exporting this data into RDF and integrating with related data and vocabularies in triple stores such as Sesame, AllegroGraph and Virtuoso. Early days, still climbing the learning curve with this!
- Experimenting with exporting this data into RDF and integrating with related data and vocabularies in triple stores such as Sesame, AllegroGraph and Virtuoso. Early days, still climbing the learning curve with this!
- As we start to create these triples we can bridge the gap from the QTL and its genes to the disease, allowing the scientists to identify or prioritize candidate genes in their QTL regions (or gene lists) and save them (to some degree) from spending a lot of time manually searching databases online.
- As we start to create these triples we can bridge the gap from the QTL and its genes to the disease, allowing the scientists to identify or prioritize candidate genes in their QTL regions (or gene lists) and save them (to some degree) from spending a lot of time manually searching databases online.
- As we start to create these triples we can bridge the gap from the QTL and its genes to the disease, allowing the scientists to identify or prioritize candidate genes in their QTL regions (or gene lists) and save them (to some degree) from spending a lot of time manually searching databases online.
- As we start to create these triples we can bridge the gap from the QTL and its genes to the disease, allowing the scientists to identify or prioritize candidate genes in their QTL regions (or gene lists) and save them (to some degree) from spending a lot of time manually searching databases online.
- As we start to create these triples we can bridge the gap from the QTL and its genes to the disease, allowing the scientists to identify or prioritize candidate genes in their QTL regions (or gene lists) and save them (to some degree) from spending a lot of time manually searching databases online.
- As we start to create these triples we can bridge the gap from the QTL and its genes to the disease, allowing the scientists to identify or prioritize candidate genes in their QTL regions (or gene lists) and save them (to some degree) from spending a lot of time manually searching databases online.
- As we start to create these triples we can bridge the gap from the QTL and its genes to the disease, allowing the scientists to identify or prioritize candidate genes in their QTL regions (or gene lists) and save them (to some degree) from spending a lot of time manually searching databases online.
- Acknowledgements