

This page gives all information associated with the upcoming 2006 PSI Spring Meeting a the Hyatt Regency Hotel, San Francisco CA, USA.
Since its conception in April 2002, the HUPO Proteomics Standards Initiative has contributed to the development of community standards for proteomics in a collaborative and very dynamic way, resulting in several published reports. Following the initial release in 2004, the MI work group has now released version 2.5 of the PSI MI standard for molecular interactions, and the mzData 1.05 standard for mass spectra has been widely implemented by instrument vendors, tool providers and public databases.
At its third spring meeting, the Proteomics Standards Initiative will formalise its structure, further develop its core standards, and provide a platform for scientific exchange with related fields beyond proteomics. Additionally, after initially operating in a very informal manner, PSI is now coming of age; with an increasing participation, increasing investment into standards by both academic and commercial entities, and growing interest by scientists, funders, and journals, the PSI needs to formalise its operations. A major topic in the common session will be a formal structure for PSI and its standardisation process.
Metabolomics: The benefits of broad cross-domain input into the standardisation process are several; data intercompatibility, speed of development and design robustness are just three. The metabolomics community will most likely adopt the mzData format, with the obvious benefits for instrument vendors, tool and database providers; a productive collaboration is also being formed to jointly advance the spML format; the vocabularies to support both spML and mzData will similarly be advanced jointly. To promote this collaboration, representatives of the Metabolomics Society have been invited to participate in the meeting.
Minimum Information About a Cellular Assay: Advances in genomics and functional genomics have enabled large scale analysis of gene and protein function by means of high throughput cell biology. Cells are perturbed in vitro and induced effects are recorded and analysed. Perturbations can be in several flavours and induced by molecules (e.g. siRNA, expression construct, small chemical compound) or numerous other stresses (e.g. temperature shift, serum starvation). Standardisation of experimental descriptions and ontologies (adopting e.g. FuGE) with help of a Minimum Information About a Cellular Assay (MIACA) will provide means to compare, exchange, and integrate data that have been acquired in different and diverse setups. Working groups for MIACA modules will be established, towards the formulation of formats and ontologies, and their integration into a community standard data model. Scientists working in the generation or analysis of data acquired in cellular assays are invited to actively participate in this effort.
The FuGE OM/ML: PSI will continue to foster discussion of implementation issues for the FuGE model (now at milestone 2), both in its native form and as a parent schema for PSI formats.
The Functional Genomics Ontology (FuGO): The meeting will feature a half day session dedicated to issues around the growth and evolution of that ontology and the relationship between PSI-generated CVs and FuGO. Ontology issues will also arise throughout the meeting, and will in part be addressed in the context of FuGO.
Henning Hermjakob
Randy Julian
Chris Taylor
John Garavelli
Robert Barkovich, Thermo Corporation
David Horn, Agilent Technologies
Sean Seymour, Applied Biosystems
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| Time | Track 1 — PSI: MI | Track 2 — PSI: MS | Track 3 — PSI: GPS | Track 4 — Satellites |
| 9:00-11:00 | Private meeting: HUPO Publications Committee |
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| 11:00-12:00 | Private meeting: PSI Steering Committee |
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| 13:00-14:00 | PSI Spring Workshop 2006 — Welcome: Chris
Taylor, EMBL-EBI |
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| 14:00-16:00 | Proteomics standards
in the laboratory workflow: |
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| 16:00-16:30 | Coffee break | |||
| 16:30-18:00 | Panel discussion – proteomics
standards in the publication process |
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| Time | Track 1 — PSI: MI | Track 2 — PSI: MS | Track 3 — PSI: GPS | Track 4 — Satellites |
| 9:00-10:00 | Formal framework for the Proteomics Standards Initiative — Structure and Process: Henning Hermjakob, EMBL-EBI |
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| 10:00-10:30 | FuGE overview and status: Angel Pizarro, U. Penn (confirmed) |
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| 10:30-11:00 | FuGO overview and status: Susanna-Assunta Sansone, EMBL-EBI (confirmed) |
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| 11:00-11:30 | Coffee break | |||
| 11:30-12:00 | MIAPE: Overview and status update: Chris Taylor, EMBL-EBI | |||
| 12:00-13:00 | PSI MOD: Protein modifications. Chair: John Garavelli, EMBL-EBI |
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| 13:00-14:00 | Lunch in hotel | |||
| 14:00-15:30 | MI schema updates. Chair: Henning Hermjakob, EMBL-EBI |
Update: status/feedback for mzData 1.05. Chair: Randy Julian, Indigo Biosystems | MIAPE: Gel Electrophoresis. Chair: Frank Gibson | MIGS and other MIxxx projects. Chair: Dawn Field, CEH Oxford |
| Discussion of the CV's OBO/RDF representation for MS. Chair: Randy Julian, Indigo Biosystems | ||||
| Comparative analysis of mzData & mzXML. Chair: Randy Julian, Indigo Biosystems | ||||
| 15:30-16:00 | Coffee break | |||
| 16:15-18:00 | Developers corner / Ontology corner | Planning for mzData 1.1: merging with mzXML. Co-chairs:
Randy Julian, Indigo Biosystems; Kent Laursen, Genologics LSS |
GelML & GIfML. Chair: Andy Jones |
FuGO. Chair: Chris Taylor, EMBL-EBI |
| Working Group Document Process (specs, MIAPE, discussion). Co-chairs: Pierre-Alain Binz, SIB/Genebio; Randy Julian, Indigo Biosystems | ||||
| Develop meeting report. Chair: Randy Julian, Indigo Biosystems | ||||
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| Time | Track 1 — PSI: MI | Track 2 — PSI: MS | Track 3 — PSI: GPS | Track 4 — Satellites |
| 9:00-10:45 | Developers corner / Ontology corner (continued) |
PSI-MSI — analysisXML: draft comments, planning, CV... | spML. Chair: Norman Paton, Uni. Manchester, UK | MIACA. Chair: Stefan Wiemann, DKFZ Heidelberg, Germany |
| 10:45-11:15 | Coffee break | |||
| 11:15-13:00 | Validation rules: specification and implementation | — continued — | MIAPE: Gel Informatics Chair: Matthias Berth, Decodon |
— continued — |
| MIAPE: Sample Processing Chair: Chris Taylor, EMBL-EBI |
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| 13:00-14:00 | Lunch in hotel | |||
| 14:00-15:45 | Summary and future planning | — continued — | GPS CVs. Chair: Chris Taylor, EMBL-EBI |
FuGE. Chair: Angel Pizarro, U. Penn |
| Final discussion | Planning session. Chair: Norman Paton, Uni. Manchester, UK |
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| 15:45-16:15 | Coffee break | |||
| 16:15-18:00 | Group and overall summaries,
planning, close of meeting. Chair: Randy Julian, Indigo Biosystems |
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Any queries regarding registration should be directed to Chris Taylor.
The meeting will be held at the Hyatt Regency San Francisco, which is accessible from both the San Francisco (SFO) and Oakland (OAK) airports. Reduced rate rooms have been allocated at the Hyatt Regency ($195 per night). To reserve, dial (+1) 800 233 1234 and state that you are attending the "HUPO-PSI meeting". Please also indicate your intention to book at the Hyatt on the registration form, by checking the appropriate box.
By far the best way to travel to the Hyatt Regency is by using BART — the Bay Area Rapid Transit subway system (http://www.bart.gov/) — from either airport. The hotel is only feet away from the exit of the Embarcadero BART stop. There are maps of the whole BART system in all trains:
Alternately, you can take taxis or one of the many shared van transport services, although these are much more expensive ($25-45) and may well be rather slower, depending on traffic.
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| Additional Sponsorship gratefully received from: Bruker [www.bruker.de], Cell Signaling Technology [www.cellsignal.com] |
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