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From: Deborah F. P. <pi...@sn...> - 2002-07-25 12:22:08
|
Hi, startRunGenerateBlastSimilarity.pl is a perl script that orchestrates blast runs on a cluster. In this case the query sequences are the assemblies and the subject databases are sequences from prodom, nrdb, or cdd. We are currenntly running the script via a controller that Steve Fischer wrote. Here is an example of an old command line that might give you some information: startRunGenerateBlastSimilarity.pl --regex '(\S+)' --blastProgram blastp --database prodom2001 --seqFile ~/BlastRuns/plas_v3.1VsProdom.cds --setsize 500 --nodes '72, 73' --blastParams 'wordmask=seg+xnu W=3 T=1000' And here is a sample output: >40142473 (0 subjects) >40142515 (0 subjects) >40142529 (0 subjects) >40142583 (0 subjects) >40142613 (1 subjects) Sum: 8022685:114:1.2e-09:7:84:2:227:2:66:33:43:1:-1 HSP1: 8022685:23:32:49:114:1.2e-09:36:84:2:148:1:-1 HSP2: 8022685:10:11:17:44:1.2e-09:7:23:177:227:1:-3 >40142617 (0 subjects) >97378349 (1 subjects) We extract the assembly, prodom, and nrdb sequences from the Assembly view of NASequenceImp and the MotifAASequence and ExternalAASequence views of AASequenceImp. We do this using another perl script, dumpSequencesFromTable.pl, so that they have GUS identifiers. CDD sequences are handled using Rps Blast so that GUSidentifiers have to be attached afterwards using substitutePrimKeysInSimilarity.pl. Finally, the resulting similarity files are loaded into the Similarity table (from which previous similarities for that taxon have been deleted) using LoadBlastSimilaritiesPK.pm. There are more details but I may have already told you more than you want to know right now. We are hard at work on a script that automates the entire DoTS build and annotation process. It is in the development stage at the moment although we are using it for a large part of the process. I hope this helps. Deborah Pinney On 25 Jul 2002, Keith James wrote: > > Hi, > > Sorry if you get this twice - the first time I posted nobody at Sanger > seemed to get my message. > > In plugins I found LoadBlastSimilaritiesPK.pm which appears to use > output from a script called generateBlastSimilarity.pl (which we do > not have). What does generateBlastSimilarity.pl do and what file > format does it produce, please? > > thanks, > > Keith > > |
From: Keith J. <kd...@sa...> - 2002-07-25 10:43:11
|
Hi, Sorry if you get this twice - the first time I posted nobody at Sanger seemed to get my message. In plugins I found LoadBlastSimilaritiesPK.pm which appears to use output from a script called generateBlastSimilarity.pl (which we do not have). What does generateBlastSimilarity.pl do and what file format does it produce, please? thanks, Keith -- - Keith James <kd...@sa...> bioinformatics programming support - - Pathogen Sequencing Unit, The Wellcome Trust Sanger Institute, UK - |
From: Matt B. <mb...@sa...> - 2002-07-24 16:00:59
|
That should be sufficient. In the GO database, there is only ever one comment per GO term. cheers Matt Sharon Diskin wrote: > Okay, thanks. Does this mean that a single comment field added to > the GOTerm table is sufficient in your view? > > Alternatively, we could use the DoTS.Comments table to store comments, > these can then be associated through the Evidence table to any row in > GUS. So, another option would be to use the Comments table to store > the text, and link it to the GOTerm entry through the Evidence table. > If this is not an appropriate use of the Evidence table, then we > could just create a GOTermComments linking table. > > cheers, > sharon > > Arnaud Kerhornou wrote: > >> Hi Sharon >> >> I forward you an example of a GO comment given by Matt. >> >> cheers >> Arnaud >> >> -------- Original Message -------- >> Subject: Re: proposed modifications to GO Schema for GUS3.0 >> Date: Tue, 16 Jul 2002 13:19:51 +0100 >> From: Matt Berriman <mb...@sa...> >> To: Arnaud Kerhornou <ax...@sa...> >> References: >> <Pin...@sn...> >> <3D2...@sa...> <3D2...@pc...> >> <3D2...@sa...> <3D2...@pc...> >> <3D3...@sa...> >> >> >> >>Here's a complete entry from the GO database: >> >>term: C-terminal protein farnesylation >> >>goid: GO:0006503 >> >>definition: The covalent or non-covalent attachment of a farnesyl moiety >>to the carboxy terminus of a protein. OBSOLETE. >> >>definition_reference: GO:jl >> >>comment: This term was made obsolete because the process is not exclusive to the carboxy terminus >>of a protein. Consider instead the biological process term 'protein amino acid farnesylation ; >>GO:0018347'. >> >>cheers >>Matt >> >> >>Arnaud Kerhornou wrote: >> >>> Sharon Diskin wrote: >>> >>>> >>>>> Also re. the GOTerm table, would it be possible to add a comment >>>>> field ? >>>> >>>> >>>> >>>> I do not have a problem with this. Does anyone else have an opinion >>>> on this? What type of information would you put in the comment field? >>> >>> >>> Matt, >>> >>> Do you have an >>exa >>mple of comment you want to store ? >>> >>> I should mention than the GO database design allows to store several >>> comments (one to many relationship), one comment field might be enough >>> though and would keep the design simple. >>> >>> cheers >>> Arnaud >>> >>>> >>>> Cheers, >>>> Sharon >>>> >>>> p.s. I will be out of town until Monday July 22nd. >>>> >>>>> >>>>> cheers >>>>> Arnaud >>>>> >>>>> Sharon Diskin wrote: >>>>> >>>>>> Hi Arnaud, >>>>>> >>>>>> I've attached the new GO schema and documentation that Jonathan >>>>>> Schug and I have come up. We believe that this new schema addresses >>>>>> your concern about the association date and also provides a better >>>>>> way of tracking multiple instances/sources of the same association >>>>> >>> (s >>ee description of GOAssociationInstance table). >>>>>> >>>>>> >>>>>> Regarding your other question concerning the 'DB:Ref' and 'from or >>>>>> with', we see these being tracked using the generic Evidence >>>>>> table. The 'from or with' would be Evidence for the >>>>>> GOAssocInstEvidCode entry as it is connected to a specific evidence >>>>>> code that is assigned to the association. The 'DB:Ref' (such as in >>>>>> the PubMed example you mentioned) would be Evidence for the >>>>>> GOAssociationInstance entry as it is _not_ connected to a specific >>>>>> evidence code, but rather the association as a whole. More details >>>>>> can be found in the attached documentation. >>>>>> >>>>>> >>>>>> Any feedback is welcome. Also, if any of this is unclear, just let >>>>>&g >>t; us know. >> >>>>>> >>>>>> Cheers, >>>>>> Sharon >>>>>> >>>>>> >>>>> >>>> >>> >>> >>> >> >>-- >> >> Dr Matthew Berriman >> Senior Computer Biologist - Pathogen Sequencing Unit - >> The Wellcome Trust Sanger Institute >> Tel +44 (0)1223 494817 - Fax +44 (0)1223 494919 >> http://www.sanger.ac.uk >>-- >>Arnaud Kerhornou >> >>The Wellcome Trust Sanger Institute >>The Pathogen Sequencing Unit >>Wellcome Trust Genome Campus, Hinxton, Cambridge, CB10 1SA, UK >>Work: +44 (0) 1223 494955 >>Fax: +44 (0) 1223 494919 >> >> >> >> >> > -- Dr Matthew Berriman Senior Computer Biologist - Pathogen Sequencing Unit - The Wellcome Trust Sanger Institute Tel +44 (0)1223 494817 - Fax +44 (0)1223 494919 http://www.sanger.ac.uk |
From: Sharon D. <di...@SN...> - 2002-07-23 16:17:36
|
Okay, thanks. Does this mean that a single comment field added to the GOTerm table is sufficient in your view? Alternatively, we could use the DoTS.Comments table to store comments, these can then be associated through the Evidence table to any row in GUS. So, another option would be to use the Comments table to store the text, and link it to the GOTerm entry through the Evidence table. If this is not an appropriate use of the Evidence table, then we could just create a GOTermComments linking table. cheers, sharon Arnaud Kerhornou wrote: > Hi Sharon > > I forward you an example of a GO comment given by Matt. > > cheers > Arnaud > > -------- Original Message -------- > Subject: Re: proposed modifications to GO Schema for GUS3.0 > Date: Tue, 16 Jul 2002 13:19:51 +0100 > From: Matt Berriman <mb...@sa...> > To: Arnaud Kerhornou <ax...@sa...> > References: > <Pin...@sn...> > <3D2...@sa...> <3D2...@pc...> > <3D2...@sa...> <3D2...@pc...> > <3D3...@sa...> > > > >Here's a complete entry from the GO database: > >term: C-terminal protein farnesylation > >goid: GO:0006503 > >definition: The covalent or non-covalent attachment of a farnesyl moiety >to the carboxy terminus of a protein. OBSOLETE. > >definition_reference: GO:jl > >comment: This term was made obsolete because the process is not exclusive to the carboxy terminus >of a protein. Consider instead the biological process term 'protein amino acid farnesylation ; >GO:0018347'. > >cheers >Matt > > >Arnaud Kerhornou wrote: > >> Sharon Diskin wrote: >> >>> >>>> Also re. the GOTerm table, would it be possible to add a comment >>>> field ? >>> >>> >>> >>> I do not have a problem with this. Does anyone else have an opinion >>> on this? What type of information would you put in the comment field? >> >> >> Matt, >> >> Do you have an exa >mple of comment you want to store ? >> >> I should mention than the GO database design allows to store several >> comments (one to many relationship), one comment field might be enough >> though and would keep the design simple. >> >> cheers >> Arnaud >> >>> >>> Cheers, >>> Sharon >>> >>> p.s. I will be out of town until Monday July 22nd. >>> >>>> >>>> cheers >>>> Arnaud >>>> >>>> Sharon Diskin wrote: >>>> >>>>> Hi Arnaud, >>>>> >>>>> I've attached the new GO schema and documentation that Jonathan >>>>> Schug and I have come up. We believe that this new schema addresses >>>>> your concern about the association date and also provides a better >>>>> way of tracking multiple instances/sources of the same association >>>>> (s >ee description of GOAssociationInstance table). >>>>> >>>>> >>>>> Regarding your other question concerning the 'DB:Ref' and 'from or >>>>> with', we see these being tracked using the generic Evidence >>>>> table. The 'from or with' would be Evidence for the >>>>> GOAssocInstEvidCode entry as it is connected to a specific evidence >>>>> code that is assigned to the association. The 'DB:Ref' (such as in >>>>> the PubMed example you mentioned) would be Evidence for the >>>>> GOAssociationInstance entry as it is _not_ connected to a specific >>>>> evidence code, but rather the association as a whole. More details >>>>> can be found in the attached documentation. >>>>> >>>>> >>>>> Any feedback is welcome. Also, if any of this is unclear, just let >>>>> us know. > >>>>> >>>>> Cheers, >>>>> Sharon >>>>> >>>>> >>>> >>> >> >> >> > >-- > > Dr Matthew Berriman > Senior Computer Biologist - Pathogen Sequencing Unit - > The Wellcome Trust Sanger Institute > Tel +44 (0)1223 494817 - Fax +44 (0)1223 494919 > http://www.sanger.ac.uk >-- >Arnaud Kerhornou > >The Wellcome Trust Sanger Institute >The Pathogen Sequencing Unit >Wellcome Trust Genome Campus, Hinxton, Cambridge, CB10 1SA, UK >Work: +44 (0) 1223 494955 >Fax: +44 (0) 1223 494919 > > > > > |
From: Sharon D. <di...@SN...> - 2002-07-23 15:51:33
|
Hi Folks, I've attached our latest requirements spec for the annotator interface. Notably missing from this document are the details regarding the GUI and some specifics for how we envision external tools being run from within the interface (such as Blast for example). We are in the process of working out some details in these areas and we would be happy to share our thoughts with you if this is something you are interested in. What you will find in this document is a complete list of the annotation tasks we plan to include as well as some high level requirements that support the annotation tasks. As Joan mentioned in the teleconference, we will likely focus on those tasks termed "surface level" as a first pass/version of a new tool. Cheers, Sharon |
From: Angel P. <an...@sn...> - 2002-07-22 18:57:01
|
Could we add a 'contact_type' column to SRes.Contact so that we can differnetiate between organizations and people? This is basically either a bit column or enumeration ('person'|'organization') but it makes export to MAGE (and other object models that differentiate between the two) much easier. Angel |
From: Angel P. <an...@sn...> - 2002-07-22 14:22:52
|
I added the sequences for Core, SRes and DoTS into the sourceforge.net CVS. Basically just relpaced the empty files that were there already. Also welcome debbie pinney to the sourceforge developer team! Angel |
From: Pjm <pj...@sa...> - 2002-07-19 14:27:16
|
Hi Jonathan, I have attached the PL/SQL scripts to dump everything in the correct order. I include what our DBA said on how to run it. Please email me or Martin the DBA (md...@sa...) if you have any questions. Since we need to get started on importing data into GUS we need to use GUSdev. The schema we have is not in sync with the website code (remember, we had errors because tables did not exist in the GUS import). Could we get a copy of the DB and the website code (plus perl layer). I hope this is not asking too much - you could test the PL/SQL to see if it works! thanks, Paul. ---------------- Its a PL/SQL package that can be installed on any database that it is needed on. It can be called by a simple script such as :- --run_cps.sql -- set serveroutput on size 100000 spool cre_eric.sql execute schema_copy.cp_schema('ENTMAN','USERS','INDX','ERIC','RED','GUS',128) spool off The above eg duplicates the "entman" schema into user "eric" identified by "red", using tablespaces "users" and "indx" and defaulting all objects to "128k" intitial and next. The script can be changed to run for multiple users, spool the various outputs and probably kick it off at the end. ---- As a side issue, if you have a fragmented database this code will calculate the size of the extents |
From: Chris S. <sto...@sn...> - 2002-07-19 13:56:58
|
Paul, Will try to meet on this Monday and have an answer for our conference call (I'm out of town today). For mid-September my guess is GUS3.0 but that's a guess. Cheers, Chris On Thu, 18 Jul 2002, pjm wrote: > Hi all, > > we would like to use GUS30 schema to load data into it and, in a couple > of weeks time, use the code for the AllGenes website to query that > data. We are not sure how far along you are porting over the perl > code, in particular the dbiperl_utils modules and the GA plugins - > here are the main ones of interest; > > UpdateGUSFromXML.pm (will need XML too for taxon table) > LoadGoOntology.pm > Swall & EMBL plugins > SO - can we use the same plugin as GO or do we need a new one? > > We would like to be able to show basic querying by mid-September (for > the Woods Hole meeting) - the results can just be links to gene pages > in www.genedb.org for now - but obviously we need to make a start very > soon. > > Should we go with GUSdev or GUS30? > > Also the Oracle sequences are not present in Sourceforge, please could you add > them. Our Oracle DBA has finished the PL/SQL script for exporting everything in > the correct order, I hope to give you more details tomorrow. > > Paul. > > > ------------------------------------------------------- > This sf.net email is sponsored by:ThinkGeek > Welcome to geek heaven. > http://thinkgeek.com/sf > _______________________________________________ > Gusdev-gusdev mailing list > Gus...@li... > https://lists.sourceforge.net/lists/listinfo/gusdev-gusdev > -- Chris Stoeckert, Ph.D. Research Associate Professor, Dept. of Genetics Center for Bioinformatics, University of Pennsylvania 418 Guardian Dr., Philadelphia, PA 19104 Ph: 215-573-4409 FAX:215-573-3111 |
From: pjm <pj...@sa...> - 2002-07-18 19:56:37
|
Hi all, we would like to use GUS30 schema to load data into it and, in a couple of weeks time, use the code for the AllGenes website to query that data. We are not sure how far along you are porting over the perl code, in particular the dbiperl_utils modules and the GA plugins - here are the main ones of interest; UpdateGUSFromXML.pm (will need XML too for taxon table) LoadGoOntology.pm Swall & EMBL plugins SO - can we use the same plugin as GO or do we need a new one? We would like to be able to show basic querying by mid-September (for the Woods Hole meeting) - the results can just be links to gene pages in www.genedb.org for now - but obviously we need to make a start very soon. Should we go with GUSdev or GUS30? Also the Oracle sequences are not present in Sourceforge, please could you add them. Our Oracle DBA has finished the PL/SQL script for exporting everything in the correct order, I hope to give you more details tomorrow. Paul. |
From: Arnaud K. <ax...@sa...> - 2002-07-18 08:45:10
|
Hi Sharon I forward you an example of a GO comment given by Matt. cheers Arnaud -------- Original Message -------- Subject: Re: proposed modifications to GO Schema for GUS3.0 Date: Tue, 16 Jul 2002 13:19:51 +0100 From: Matt Berriman <mb...@sa...> To: Arnaud Kerhornou <ax...@sa...> References: <Pin...@sn...> <3D2...@sa...> <3D2...@pc...> <3D2...@sa...> <3D2...@pc...> <3D3...@sa...> Here's a complete entry from the GO database: term: C-terminal protein farnesylation goid: GO:0006503 definition: The covalent or non-covalent attachment of a farnesyl moiety to the carboxy terminus of a protein. OBSOLETE. definition_reference: GO:jl comment: This term was made obsolete because the process is not exclusive to the carboxy terminus of a protein. Consider instead the biological process term 'protein amino acid farnesylation ; GO:0018347'. cheers Matt Arnaud Kerhornou wrote: > Sharon Diskin wrote: > >> >>> Also re. the GOTerm table, would it be possible to add a comment >>> field ? >> >> >> >> I do not have a problem with this. Does anyone else have an opinion >> on this? What type of information would you put in the comment field? > > > Matt, > > Do you have an example of comment you want to store ? > > I should mention than the GO database design allows to store several > comments (one to many relationship), one comment field might be enough > though and would keep the design simple. > > cheers > Arnaud > >> >> Cheers, >> Sharon >> >> p.s. I will be out of town until Monday July 22nd. >> >>> >>> cheers >>> Arnaud >>> >>> Sharon Diskin wrote: >>> >>>> Hi Arnaud, >>>> >>>> I've attached the new GO schema and documentation that Jonathan >>>> Schug and I have come up. We believe that this new schema addresses >>>> your concern about the association date and also provides a better >>>> way of tracking multiple instances/sources of the same association >>>> (see description of GOAssociationInstance table). >>>> >>>> >>>> Regarding your other question concerning the 'DB:Ref' and 'from or >>>> with', we see these being tracked using the generic Evidence >>>> table. The 'from or with' would be Evidence for the >>>> GOAssocInstEvidCode entry as it is connected to a specific evidence >>>> code that is assigned to the association. The 'DB:Ref' (such as in >>>> the PubMed example you mentioned) would be Evidence for the >>>> GOAssociationInstance entry as it is _not_ connected to a specific >>>> evidence code, but rather the association as a whole. More details >>>> can be found in the attached documentation. >>>> >>>> >>>> Any feedback is welcome. Also, if any of this is unclear, just let >>>> us know. >>>> >>>> Cheers, >>>> Sharon >>>> >>>> >>> >> > > > -- Dr Matthew Berriman Senior Computer Biologist - Pathogen Sequencing Unit - The Wellcome Trust Sanger Institute Tel +44 (0)1223 494817 - Fax +44 (0)1223 494919 http://www.sanger.ac.uk -- Arnaud Kerhornou The Wellcome Trust Sanger Institute The Pathogen Sequencing Unit Wellcome Trust Genome Campus, Hinxton, Cambridge, CB10 1SA, UK Work: +44 (0) 1223 494955 Fax: +44 (0) 1223 494919 |
From: Arnaud K. <ax...@sa...> - 2002-07-16 09:17:24
|
Sharon Diskin wrote: > >> Also re. the GOTerm table, would it be possible to add a comment field ? > > > I do not have a problem with this. Does anyone else have an opinion > on this? What type of information would you put in the comment field? Matt, Do you have an example of comment you want to store ? I should mention than the GO database design allows to store several comments (one to many relationship), one comment field might be enough though and would keep the design simple. cheers Arnaud > > Cheers, > Sharon > > p.s. I will be out of town until Monday July 22nd. > >> >> cheers >> Arnaud >> >> Sharon Diskin wrote: >> >>> Hi Arnaud, >>> >>> I've attached the new GO schema and documentation that Jonathan >>> Schug and I have come up. We believe that this new schema addresses >>> your concern about the association date and also provides a better >>> way of tracking multiple instances/sources of the same association >>> (see description of GOAssociationInstance table). >>> >>> >>> Regarding your other question concerning the 'DB:Ref' and 'from or >>> with', we see these being tracked using the generic Evidence >>> table. The 'from or with' would be Evidence for the >>> GOAssocInstEvidCode entry as it is connected to a specific evidence >>> code that is assigned to the association. The 'DB:Ref' (such as in >>> the PubMed example you mentioned) would be Evidence for the >>> GOAssociationInstance entry as it is _not_ connected to a specific >>> evidence code, but rather the association as a whole. More details >>> can be found in the attached documentation. >>> >>> >>> Any feedback is welcome. Also, if any of this is unclear, just let >>> us know. >>> >>> Cheers, >>> Sharon >>> >>> >> > |
From: Sharon D. <di...@SN...> - 2002-07-12 21:56:50
|
Hi Arnaud, Thanks for the quick review. Arnaud Kerhornou wrote: > Hi Sharon > > I had a discussion with Matt and from our point of view, the design > you're proposing sounds sensible. > > Just two clarifications about evidences: > > (1) for an evidence attached to a GOAssociationInstance, it can be: > * Similarity data, > * a AAMotifGORule, > * a DB Reference, stored in an ExternalDBEntry if it's external, > * if it's a pubmed_id, we may want to store the whole reference > into a reference entry. But I guess it can be done with the schema > you're proposing, is that right ? That is correct. Since we're using the generic Evidence table, the "fact_table" could be any table in GUS. There are no constraints that force you to have all the DB refereneces stored in an ExternalDBEntry. > > (2) for an evidence attached to a GOAssocInstEvidenceCode as it may > be an "internal DB link", e.g. a protein_id for example, the DB name > prefix will be GeneDB in our case, or if it's a GO_id, it will be GO > as a prefix. Will it be generated on the fly ? I would view this as something generated on the fly. I suppose for external databases (such as GO), we could add an attribute to the ExternalDatabase table that represents the "abbreviated name". This abbreviated name could then be used to prefix identifiers. > > Also re. the GOTerm table, would it be possible to add a comment field ? I do not have a problem with this. Does anyone else have an opinion on this? What type of information would you put in the comment field? Cheers, Sharon p.s. I will be out of town until Monday July 22nd. > > cheers > Arnaud > > Sharon Diskin wrote: > >> Hi Arnaud, >> >> I've attached the new GO schema and documentation that Jonathan Schug >> and I have come up. We believe that this new schema addresses your >> concern about the association date and also provides a better way of >> tracking multiple instances/sources of the same association (see >> description of GOAssociationInstance table). >> >> >> Regarding your other question concerning the 'DB:Ref' and 'from or >> with', we see these being tracked using the generic Evidence table. >> The 'from or with' would be Evidence for the GOAssocInstEvidCode >> entry as it is connected to a specific evidence code that is assigned >> to the association. The 'DB:Ref' (such as in the PubMed example you >> mentioned) would be Evidence for the GOAssociationInstance entry as >> it is _not_ connected to a specific evidence code, but rather the >> association as a whole. More details can be found in the attached >> documentation. >> >> >> Any feedback is welcome. Also, if any of this is unclear, just let >> us know. >> >> Cheers, >> Sharon >> >> > > > |
From: Arnaud K. <ax...@sa...> - 2002-07-12 16:23:03
|
Hi Sharon I had a discussion with Matt and from our point of view, the design you're proposing sounds sensible. Just two clarifications about evidences: (1) for an evidence attached to a GOAssociationInstance, it can be: * Similarity data, * a AAMotifGORule, * a DB Reference, stored in an ExternalDBEntry if it's external, * if it's a pubmed_id, we may want to store the whole reference into a reference entry. But I guess it can be done with the schema you're proposing, is that right ? (2) for an evidence attached to a GOAssocInstEvidenceCode as it may be an "internal DB link", e.g. a protein_id for example, the DB name prefix will be GeneDB in our case, or if it's a GO_id, it will be GO as a prefix. Will it be generated on the fly ? Also re. the GOTerm table, would it be possible to add a comment field ? cheers Arnaud Sharon Diskin wrote: > Hi Arnaud, > > I've attached the new GO schema and documentation that Jonathan Schug > and I have come up. We believe that this new schema addresses your > concern about the association date and also provides a better way of > tracking multiple instances/sources of the same association (see > description of GOAssociationInstance table). > > > Regarding your other question concerning the 'DB:Ref' and 'from or > with', we see these being tracked using the generic Evidence table. > The 'from or with' would be Evidence for the GOAssocInstEvidCode entry > as it is connected to a specific evidence code that is assigned to the > association. The 'DB:Ref' (such as in the PubMed example you > mentioned) would be Evidence for the GOAssociationInstance entry as it > is _not_ connected to a specific evidence code, but rather the > association as a whole. More details can be found in the attached > documentation. > > > Any feedback is welcome. Also, if any of this is unclear, just let us > know. > > Cheers, > Sharon > > |
From: Arnaud K. <ax...@sa...> - 2002-07-05 14:47:10
|
Hi everyone I would like to report a new table, ProteinProperty and new views on the top of AAFeatureImp table for protein features such as domains. * Protein properties : There are 4 protein properties : * Isoelectric point (1), * Molecular mass (2), * Charge (3), * Average residue mass (4). The 3 first ones may have several values as they can be characterized experimentally. From a design point of view, we can have a unique ProteinProperty table or a view foreach proterty (a ProteinPropertyImp table and three views: IsoElectricPointProperty, MolecularMassProperty and ChargeProperty). The number of properties may not changed in the future so I may be simpler to create a unique ProteinProperty table. Specification => A property would behave like a feature, ie : * it is attached to a sequence modulo the fact it doesn't have a location within it, * it can be supported by evidences such as an experiment, published or from a personal communication. * have external db refs. ProteinProperty table: * protein_property_id : number * property_name : varchar2(50) * property_value : number (5) * & stuff common to any GUS table: modification_date ... The 4th property, average residue mass, could be an extra attribute in the proteinSequence or TranslatedAASequence view. ****************** * Protein Features : Features attached to a protein sequence. The new features objects are: (1) Signal Peptide Feature : It's already a view in GUS, but we will store curated data, such as targetting information. (2) Domains: It can be: * a Leucine Zipper domain, * a coiled-coil domain, * a Pfam, Smart or Prosite domain. DomainFeature view: * aa_feature_id : number (10), * aa_sequence_id : number (10), * name : varchar2 (50), * description : varchar2 (100), * score : number (4) * e_value : number (10), + external database link entries and a location object. (3) Transmenbrane domain feature: Question : PlasmoDB web site shows hydrophobicity graphics, where is it stored in GUS ? (4) Post-translational modification feature: * type : varchar2 (50) (e.g. glycosylation, phosphorylation ...) * modified_by : use of the Interaction table ? * Coordinates of the phosphorylation site in a AALocation object. (5) Repeat Features, should be the same design that at the DNA level : * RepeatRegionFeature as a set of RepeatUnitFeatures, * RepeatUnitFeature, with the consensus sequence, name and size * RepeatType table Another question : What about 2D structures (beta-sheet and alpha-helice) in GUS ? Let me know if you have any comments. I'll send another email for extra features at the DNA/RNA level. Cheers Arnaud |
From: Arnaud K. <ax...@sa...> - 2002-07-04 18:14:22
|
Hi Chris Sounds good. See below for some comments. Chris Stoeckert wrote: > Hi All, > Here are the phenotype tables I mentioned during the conference call. > I still need to look at the rest of the schema to see how best to link > it to gene sequences but welcome suggestions. We would use it to annotate alleles. I guess a new table is needed with the allele name, the degree of dominance, mutation data, complementation data ... > > Also, Angel has posted a picture of a proposed schema for capturing > mass spec data at: > http://www.cbil.upenn.edu/downloads/Proteomics/schema/ > Next steps are to have people look it over and try to fit available > data into it. > > Finally, I will write up my notes of our conference call and send to > Marie-Adele to edit and pass around (if she agrees ;-) ). > > Cheers, > Chris > > Phenotype: A linking table in the spirit of GOBO or PATO constructing > phenotypic descriptions from orthogonal ontologies using nounal phrases. > phenotype_id > pato_attribute_id > anatomy_id > cell_type_id can point to the Anatomy table > dev_stage_id > description varchar 255 text description of what the terms > represent in aggregate At the moment, as pombe, Trypanosoma and Leish are unicellular, the orthologous ontologies we would use are GO process and GO component, as well as the Parasite life cycle ontology being developed here by Mat. Berriman. > > PATOAttribute: A > pato_attribute_id > term_name varchar255 > term_synonym varchar 255 > version varchar 50 > parent_pato_attribute_id term_type varchar 20 "attribute", > "attribute value" So to summarize a phenotype is made from a set of ontology terms, there is a many to many relationship between each of these orthogonal ontologies and the Phenotype table. It also has a set of attributes, and each attribute is associated to a set of attribute values. cheers Arnaud Note this is based on Michael Ashburner's draft. ---------- On the representation of phenotypic data in genome databases - pato.ontology. A discussion paper. Version 2.0 22 February 2002. Michael Ashburner, FlyBase. pato: phenotype & trait ontology. This paper assumes some knowledge of the work of the Gene Ontology Consortium - see www.geneontology.org. A major conceptual and practical problem that faces all genomic databases is how to describe mutant phenotypes (I include in this term epigenetic phenotype due to RNAi, for example, and the more general class of traits, in the sense this word is used by plant and animal breeders). Some databases are, I know, struggling to find a solution to this problem, these include FlyBase, Gramene, the Mouse Genome Database, and others. Traditionally, phenotypes have been described as free text, for example in some FlyBase tables and in the Mouse Locus Catalog. This is great, but is obviously a poor solution if the data are to be efficiently analysed (e.g. by a search engine) computationally. I am not wholly convinced that we can ever get away from free text, at the very least as a "gloss" on a more systematic representation of these data. Nevertheless, the effort to represent these data systematically is very much worth while, and is again - I maintain - an effort that it is far better we do collaboratively, arriving at common standards, that independently. If this works it also has the consequence that rigorous queries across databases could be made (as now with GO). The core of my proposal is that phenotypic data can be represented as qualifications of descriptive nouns or nounal phrases. A typical descriptive noun would be "eye" or "leaf" or "wing development". For each class of such nouns there will be a finite (I hope) set of relevant attributes. For these examples attributes could include: shape, color, size; for "leaf" they could include: thickness, pilosity, for "wing development" they could include "abnormal". For each attribute there will be a finite (I hope) set of values. For the attribute color, for example, values would include: black, white, green. For each value there will be a finite (I hope) set of qualifiers, for green these may include dark, light. Using these three semantic classes we have, I think, the basis for the systematic description of phenotypes. The only extra need is to be able to describe the assay by means of which the phenotypes (i.e. values) were determined and the conditions, both environmental and genetic, under which the assay was performed. I will not consider assays and their conditions in this paper, since these are very much a concern of the MGED group and we should share their work (see www.mged.org). I see pato as being used to annotate (a) alleles and (b) "strains" or "lines" of an organism (e.g. for crop plants or posssibly mouse strains). I should say that I do not regard pato as the place for what (albeit loosely) we normally consider as attributes of alleles: e.g recessive, dominant, cold-sensitive, although pato should be designed to store phenotypic data that is conditional on an environmental condition (or background genotype). I am also aware that keeping pato in a flat file may be a challenge and that a more sophistical mechanism (?DAML+oil) may be needed. The purpose of sending this out at this preliminary stage is to get feedback, both at the conceptual and detailed levels. I thank John Walshaw, Suzi Lewis, Pankaj Jaiswal, Judy Blake and my Cambridge FlyBase curators (Rachel Drysdale, Gillian Milburn, Chihiro Yamada and Aubrey de Grey) for input & ideas. I have made _no_ attempt to make pato.ontology v.1.0 anything like complete - especially with respect to attribute values. We are experimenting now with re-casting some FlyBase annotation using pato.ontology, and will report. Please feel free to redistribute this to anyone who might give feedback. Distribution list at end of this file. If you never want to be bothered my me again, send me an email to that effect. Michael. The nouns/nounal phrases. ------------------------- These will be terms from an orthogonal ontology, for example the GO biological_process ontology, the GO cellular_component ontology or a species specific anatomy ontology (see go/anatomy for the Drosophila and Arabidopsis anatomy ontologies; mouse, worm and Monocot anatomies are on their way). The attributes. --------------- The hardest job will be to make a classification of attributes. A very first step is given below. We will then need a syntax for declaring for which nouns/nounal phrases a particular attribute (and its child attributes) can be used. For exampe attributes of size are of obviously relevant to anatomical structures, but not to a process such as "flight behavior". Their values. ------------- The second task is to determine the list of values any attribute may have. I have shown a few of these in pato.ontology. Their qualifiers. ----------------- Finally, we would need to determine the qualifiers that are relevant (allowed) for any particular attribute. Thus the qualifie fully would be relevant to a fertility attribute, but not to an attribute of size. I present first a "schema" of the relationships between these concepts: !antonym !antonym | | {mayhave} {has} | | concept <-{usedfor}--%attribute ---{has}---> <value ---{has}---> .qualifier | | {determinedby} | {mayhave} | | | units | assay ---{constrainedby}---> conditions ---{oftype}---> [MGED]environmental&|genetic attribute|value|qualifier ---{have}---> synonyms. concept is a concept (term) from another (orthogonal) ontology. In the draft pato.ontology: % is for attributes, < is for values of attributes |
From: Chris S. <sto...@SN...> - 2002-07-03 21:59:45
|
Hi All, Here are the phenotype tables I mentioned during the conference call. I=20= still need to look at the rest of the schema to see how best to link it=20= to gene sequences but welcome suggestions. Also, Angel has posted a picture of a proposed schema for capturing mass=20= spec data at: http://www.cbil.upenn.edu/downloads/Proteomics/schema/ Next steps are to have people look it over and try to fit available data=20= into it. Finally, I will write up my notes of our conference call and send to=20 Marie-Adele to edit and pass around (if she agrees ;-) ). Cheers, Chris Phenotype: A linking table in the spirit of GOBO or PATO constructing=20 phenotypic descriptions from orthogonal ontologies using nounal phrases. phenotype_id pato_attribute_id anatomy_id cell_type_id can point to the Anatomy table dev_stage_id description varchar 255 text description of what the terms = represent=20 in aggregate PATOAttribute: A pato_attribute_id term_name varchar255 term_synonym varchar 255 version varchar 50 parent_pato_attribute_id =09 term_type varchar 20 "attribute", "attribute value" Note this is based on Michael Ashburner's draft. ---------- On the representation of phenotypic data in genome databases -=20 pato.ontology. A discussion paper. Version 2.0 22 February 2002. Michael Ashburner, FlyBase. pato: phenotype & trait ontology. This paper assumes some knowledge of the work of the Gene Ontology Consortium - see www.geneontology.org. A major conceptual and practical problem that faces all genomic=20 databases is how to describe mutant phenotypes (I include in this term epigenetic=20 phenotype due to RNAi, for example, and the more general class of traits, in the=20= sense this word is used by plant and animal breeders). Some databases are, I=20= know, struggling to find a solution to this problem, these include FlyBase,=20 Gramene, the Mouse Genome Database, and others. Traditionally, phenotypes have=20= been described as free text, for example in some FlyBase tables and in the=20 Mouse Locus Catalog. This is great, but is obviously a poor solution if the=20= data are to be efficiently analysed (e.g. by a search engine) computationally. I=20= am not wholly convinced that we can ever get away from free text, at the very=20= least as a "gloss" on a more systematic representation of these data.=20 Nevertheless, the effort to represent these data systematically is very much worth while,=20= and is again - I maintain - an effort that it is far better we do=20 collaboratively, arriving at common standards, that independently. If this works it also has the consequence that rigorous queries across databases could be made (as now with GO). The core of my proposal is that phenotypic data can be represented as qualifications of descriptive nouns or nounal phrases. A typical=20 descriptive noun would be "eye" or "leaf" or "wing development". For each class of=20= such nouns there will be a finite (I hope) set of relevant attributes. For=20 these examples attributes could include: shape, color, size; for "leaf" they=20= could include: thickness, pilosity, for "wing development" they could include "abnormal". For each attribute there will be a finite (I hope) set of=20 values. For the attribute color, for example, values would include: black,=20 white, green. For each value there will be a finite (I hope) set of qualifiers, for=20 green these may include dark, light. Using these three semantic classes we have, I think, the basis for the systematic description of phenotypes. The only extra need is to be=20 able to describe the assay by means of which the phenotypes (i.e. values) were determined and the conditions, both environmental and genetic, under=20 which the assay was performed. I will not consider assays and their conditions=20= in this paper, since these are very much a concern of the MGED group and we=20 should share their work (see www.mged.org). I see pato as being used to annotate (a) alleles and (b) "strains" or=20 "lines" of an organism (e.g. for crop plants or posssibly mouse strains). I should say that I do not regard pato as the place for what (albeit=20 loosely) we normally consider as attributes of alleles: e.g recessive, dominant, cold-sensitive, although pato should be designed to store phenotypic=20 data that is conditional on an environmental condition (or background genotype). I am also aware that keeping pato in a flat file may be a challenge and=20= that a more sophistical mechanism (?DAML+oil) may be needed. The purpose of sending this out at this preliminary stage is to get feedback, both at the conceptual and detailed levels. I thank John Walshaw, Suzi Lewis, Pankaj Jaiswal, Judy Blake and my=20 Cambridge FlyBase curators (Rachel Drysdale, Gillian Milburn, Chihiro Yamada and=20= Aubrey de Grey) for input & ideas. I have made _no_ attempt to make=20 pato.ontology v.1.0 anything like complete - especially with respect to attribute values. We are experimenting now with re-casting some FlyBase annotation using pato.ontology, and will report. Please feel free to redistribute this to=20= anyone who might give feedback. Distribution list at end of this file. If you=20= never want to be bothered my me again, send me an email to that effect. Michael. The nouns/nounal phrases. ------------------------- These will be terms from an orthogonal ontology, for example the GO biological_process ontology, the GO cellular_component ontology or a=20 species specific anatomy ontology (see go/anatomy for the Drosophila and=20 Arabidopsis anatomy ontologies; mouse, worm and Monocot anatomies are on their way). The attributes. --------------- The hardest job will be to make a classification of attributes. A very=20= first step is given below. We will then need a syntax for declaring for which nouns/nounal phrases a particular attribute (and its child attributes)=20= can be used. For exampe attributes of size are of obviously relevant to=20 anatomical structures, but not to a process such as "flight behavior". Their values. ------------- The second task is to determine the list of values any attribute may=20 have. I have shown a few of these in pato.ontology. Their qualifiers. ----------------- Finally, we would need to determine the qualifiers that are relevant=20 (allowed) for any particular attribute. Thus the qualifie fully would be relevant=20= to a fertility attribute, but not to an attribute of size. I present first a "schema" of the relationships between these concepts: !antonym = !antonym | | {mayhave} = {has} | | concept <-{usedfor}--%attribute ---{has}---> <value ---{has}--->=20 .qualifier | | {determinedby} | {mayhave} | | | units | assay ---{constrainedby}--->=20 conditions ---{oftype}---> [MGED]environmental&|genetic attribute|value|qualifier ---{have}---> synonyms. concept is a concept (term) from another (orthogonal) ontology. In the draft pato.ontology: % is for attributes, < is for values of=20 attributes ## FlyBase: Bill Gelbart <ge...@mo...> FlyBase: Suzanna Lewis <su...@fr...> FlyBase: Chris Mungal <cj...@bd...> Mouse GI: Judy Blake <jb...@in...> Mouse: Jonathan Bard <J....@ed...> German Mouse ENU project: Martin Hrab=C8 de Angelis <hr...@gs...> MRC ENU project: Steve Brown <br...@ha...> Baylor ENU: Monica Justise <mju...@bc...> SGD: Mike Cherry <ch...@ge...> Arabidopsis: Sue Rhee <rh...@ac...> WormDB: Erich Schwarz <em...@it...> Andrzej Kilian <a.k...@ca...> Everything: Lincoln Stein <ls...@cs...> S. pombe: John Walshaw <jo...@bi...> Gramene: Susan McCouch <sr...@co...> Gramene: Pankaj Jaiswal <pj...@co...> Rice: Richard Bruskiewich <R.B...@CG...> MaizeDB: Vincent Leszek <Le...@mi...> RatBase: Simon Twigger <si...@mc...> London Dysmorphology DB: R.M. Winter <rw...@ic...> Zebra: Pat Edwards <ed...@uo...> Zebra: Mont Westerfield <mo...@uo...> MGED: Chris Stoeckert <sto...@SN...> MGED: Helen Parkinson <par...@eb...> ---------- X-Sun-Data-Type: default X-Sun-Data-Description: default X-Sun-Data-Name: pato.ontology X-Sun-Charset: us-ascii X-Sun-Content-Lines: 170 !date: Fri Feb 22 2002 !version: $Revision: 1.0 $ $pato_attribute_ontology %quantitative_attribute %qualitative_attribute <normal <abnormal ; synonym:defective %specific_qualitative_attribute %sensitivity_attribute <sensitive <insensitive ; synonym:resistant <tolerant <intolerant <responsive <unresponsive %photosensitivity_attribute <photosensitive <photoinsensitive ; synonym:photoresistant %thermosensitivity_attribute <thermosensitive <thermoinsensitive ; synonym:thermoresistant %chemical_sensitivity_attribute %drug sensitivity_attribute <drug sensitive <drug insensitive ; synonym:drug resistant %odor_attribute %flavor_attribute %color_attribute %color_hue_attribute <white ; synonym:#FFFFFF <black ; synonym:#000000 <red ; synonym:#FF0000 <green ; synonym:#00FF00 <blue ; synonym:#0000FF <yellow ; synonym:#FFFF00 <cyan ; synonym:#00FFFF <magenta ; synonym:#FF00FF %color_intensity_attribute <bright <dim %color_saturation_attribute <pale <dark %other_color_attribute <spotted <variegated ; synonym:mottled (sensu Drosophila) <blotchy <irregular <discolored <pigmented <unpigmented %aspect_of_mass_attribute %size_attribute %absolute_size_attribute %relative_size_attribute <large ; synonym:enlarged ; synonym:big ; synonym:great <small ; synonym:tiny <vestigial %mass_attribute %absolute_mass_attribute %relative_mass_attribute <large <small %weight_attribute <heavy <light %height_attribute %thickness_attribute <thick <thin %width_attribute <wide <narrow %volume_attribute %texture_attribute <smooth <rough %pilosity_attribute <hairy <glabrous <pubescent %activity_attribute <hypoactive <hyperactive <impaired <coordinated <uncoordinated <paralysed <bang sensitive %speed_attribute <fast <slow %spatial_attribute %placement_attribute ; synonym:positional_attribute <misplaced <localised <unlocalised <exserted <inserted %closure_attribute <open <closed ; synonym:blocked %angle_attribute <acute <obtuse %morphological_attribute %shape_attribute <round <square <oblate <pinnate <branched <unbranched <cleft %temperature_attribute %absolute_temperature_attribute %relative_temperature_attribute <hot <cold %temporal_attribute ; synonym:event_attribute %absolute_temporal_attribute %relative_temporal_attribute <early ; synonym:premature <late ; synonym:retarded <arrested <continuous <discontinuous %yield_attribute <low yield <high yield %compositional_attribute %metabolite_compositional_attribute %electrolyte_compositional_attribute %macromolecular_compositional_attribute %enzyme_compositional_attribute %nutritional_attribute <auxotroph <prototroph %life_span__attribute %viability_attribute <viable <lethal %fertility_attribute %male_fertility_attribute <male fertile <male infertile ; synonym:male sterile %female_fertility_attribute <female fertile <female infertile ; synonym:female sterile %hybrid_fertility_attribute %F1_fertility_attribute <F1 fertile <F1 infertile ; synonym:F1 sterile %F2_fertility_attribute <F2 fertile <F2 infertile ; synonym:F2 sterile %backcross_fertility_attribute <backcross fertile <backcross infertile ; synonym:backcross sterile %intercross_fertility_attribute <intercross fertile <intercross infertile ; synonym:intercross sterile %cytoplasmic_infertility_attribute %germ_line_dependent_fertility_attribute %soma_dependent_fertility_attribute %compatability_attribute <compatible <incompatible %gametophytic_compatability_attribute %sporphytic_compatability_attribute |
From: Pjm <pj...@sa...> - 2002-07-02 16:26:19
|
Steve, I have just talked to James Cuff (ja...@sa...). Because the ssh accounts will be very restrictive (you can't cd out of your home dir) you will not be able to change files in the repository. The Ensembl people who share this system also can not get to the repository. All requests have to go through James and his team: ss...@sa.... As long as the requests don't come thick and fast he is quite happy to make changes for us. Is this a deal breaker? As for service levels, the policy for all Sanger systems is "best efforts" - no SLA's exist here. Now I have said that, the service from all sys admins here is excellent and they are quite prepared to fix things at 1am on a Saturday morning if things go wrong (they have good financial incentives plus time of work to do this :) I can understand any misgivings you may have over what I have described so please discuss with your team and let me know what your thoughts are. Paul. Steve Fischer wrote: > jonathan crabtree cra...@pc..., 215 573-3115 > steve fischer sfi...@pc..., 215 573-2280 > deborah pinney pi...@pc... 215 573-3116 > chris stoeckert sto...@pc... 215 573-4409 > jonathan schug js...@pc... 215-573-3113 > angel pizarro an...@pc... 215 573-3114 > > > > Pjm wrote: > >> >> The following users have been created in the external repos. >> >> > pjm >> > kmr >> > axk >> > art >> > adh >> > ejz >> >> I did request the following but the sys admins would like names and >> contact info before creating them. Please send this info to me. If you >> would like to change users name let me know. Also anyone not on this >> list please let me know your user name, name and contact details. I >> will tell you know your passwords via the conference call tomorrow. >> >> > crabtree >> > fischer >> > pinney >> > stoeckrt >> > schug >> >> Paul. >> >> >> >> ------------------------------------------------------- >> This sf.net email is sponsored by:ThinkGeek >> Welcome to geek heaven. >> http://thinkgeek.com/sf >> _______________________________________________ >> Gusdev-gusdev mailing list >> Gus...@li... >> https://lists.sourceforge.net/lists/listinfo/gusdev-gusdev >> >> > > > > > ------------------------------------------------------- > This sf.net email is sponsored by:ThinkGeek > Welcome to geek heaven. > http://thinkgeek.com/sf > _______________________________________________ > Gusdev-gusdev mailing list > Gus...@li... > https://lists.sourceforge.net/lists/listinfo/gusdev-gusdev > |
From: Chris S. <sto...@SN...> - 2002-07-01 18:42:23
|
> Hi, > > am I right in thinking the only dependencies are from DOTS to CORE, > SRES to CORE > etc, so they are one way? I ask because we would like scripts to > recreate the > schema in a new instance but this depends on no inter dependencies. Hi Paul, Yes, I believe. Core should be created first, then SRes, then RAD and DoTS (I don't see any dependencies between DoTS and RAD in the current GUS3.0). Chris |
From: Steve F. <st...@SN...> - 2002-07-01 17:29:05
|
jonathan crabtree cra...@pc..., 215 573-3115 steve fischer sfi...@pc..., 215 573-2280 deborah pinney pi...@pc... 215 573-3116 chris stoeckert sto...@pc... 215 573-4409 jonathan schug js...@pc... 215-573-3113 angel pizarro an...@pc... 215 573-3114 Pjm wrote: > > The following users have been created in the external repos. > > > pjm > > kmr > > axk > > art > > adh > > ejz > > I did request the following but the sys admins would like names and > contact info before creating them. Please send this info to me. If you > would like to change users name let me know. Also anyone not on this > list please let me know your user name, name and contact details. I > will tell you know your passwords via the conference call tomorrow. > > > crabtree > > fischer > > pinney > > stoeckrt > > schug > > Paul. > > > > ------------------------------------------------------- > This sf.net email is sponsored by:ThinkGeek > Welcome to geek heaven. > http://thinkgeek.com/sf > _______________________________________________ > Gusdev-gusdev mailing list > Gus...@li... > https://lists.sourceforge.net/lists/listinfo/gusdev-gusdev > > |
From: Pjm <pj...@sa...> - 2002-07-01 16:30:12
|
The following users have been created in the external repos. > pjm > kmr > axk > art > adh > ejz I did request the following but the sys admins would like names and contact info before creating them. Please send this info to me. If you would like to change users name let me know. Also anyone not on this list please let me know your user name, name and contact details. I will tell you know your passwords via the conference call tomorrow. > crabtree > fischer > pinney > stoeckrt > schug Paul. |
From: Pjm <pj...@sa...> - 2002-07-01 15:29:52
|
Hi, am I right in thinking the only dependencies are from DOTS to CORE, SRES to CORE etc, so they are one way? I ask because we would like scripts to recreate the schema in a new instance but this depends on no inter dependencies. Our DB is confident he can have a script(s) to recreate the schemas because he has code that already does this for other DBs (Oracle 9 does something like this he thinks as standard). Thinking further down the line this would be nice for running unit tests over night, starting with a fresh DB for each test or set of tests. I have done this sort of thing in a previous life and it's very useful. The current files in cvs need to be updated though but we shall discuss in the conference call tomorrow. Paul. |
From: pjm <pj...@sa...> - 2002-06-28 09:43:56
|
Morning, I have done 2 inserts into DATABASEINFO, with primary keys of 5 and 6. Not sure why 2 DBs referenced from the core.TableInfo records. These are needed in the core-tableinfo file. Also the order in the core-tableinfo records: The tables have to be inserted first, then the views. As an example 'AAFeature' is defined before 'AAFeatureImp' but the TABLEINFO record for it says it is a view on 'AAFeatureImp' (thus failing constraint CORE.TABLEINFO_FK02). Maybe I should have loaded the bootstrap stuff before loading the constraints but I just ran it twice and excepted the error messages. Paul. |
From: pjm <pj...@sa...> - 2002-06-27 19:06:37
|
Not sure if I sent this earlier, apologies if I have.... the constraints given in the CVS files are listed in alabetical order which means I keep rerunning the file till it works - it tries to create foreign keys to not yet existing primary keys. For Oracle 8 you can dump; primary keys unique contraints foreign keys in that order. In Oracle 9 we think a fancy feature exists that works out the correct order for you or just does the above. |
From: <cra...@SN...> - 2002-06-27 15:03:13
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Paul- > we have always had a serate instance for testing and development in production > software - quite handy when some dodgy SQL brings the server to its knees. The > only thing in the code that changes is the connection to the DB itself, nothing > else. Does Oracle run on just the one machine? Right, so we could certainly solve the naming problem by requiring that people who want a second copy of the database set up a different Oracle instance for it. And if it doesn't pose an immediate problem for you I'd propose that we just not worry about the naming question for the time being. We also have two Oracle instances, one for production and one for development, running on two separate machines. However, I was thinking that we might at some point want to have two copies of GUS 3.0 on the development machine (and perhaps this is simply not the case.) We only run one Oracle instance on the development machine because there's not much point in having two; we have few enough physical disks that any dodgy SQL on the one instance would most likely affect the other one too. I also wanted to keep things as simple as possible in terms of administration. > We have scripts to dump data (all or a subset) from the live DB into the test > one so we have working real data. > > As for getting the schema into our instance, I am attempting to write a script > that will run as each user to create the nessacery tables and log what happened. > I have also come accross 2 buglets; Sounds great! > the *-indexes.sql just contain line returns or white space, not actual code. OK, I'm sure Debbie is already looking into this. > I added this line to core-tableinfo.sql; > alter session set NLS_DATE_FORMAT='YYYY-MM-DD HH24:MI:SS'; > Oracle 8 & 9 have a default date field of 'DD--MON-RR' I believe. That's my fault, sorry. We use a nonstandard default date format because I found the Oracle default too annoying when we were switching from Sybase to Oracle 8i. Jonathan -- Jonathan Crabtree Center for Bioinformatics, University of Pennsylvania 1406 Blockley Hall, 423 Guardian Drive Philadelphia, PA 19104-6021 215-573-3115 |