15:58:46 RRSAgent has joined #hcls2 15:58:46 logging to http://www.w3.org/2011/04/14-hcls2-irc 16:00:43 mscottm has joined #hcls2 16:02:48 matthias_samwald has joined #hcls2 16:04:12 bobP has joined #hcls2 16:04:17 zakim, this is tmo 16:04:17 ok, mscottm; that matches SW_HCLS(TMO)11:00AM 16:04:31 scribenick bobP 16:04:40 thanks bobP! 16:04:56 regrets: Elgar, Trish 16:05:42 bbalsa has joined #HCLS2 16:05:51 joanne has joined #hcls2 16:05:52 + +46.4.63.3.aacc 16:06:00 hello! 16:06:34 What's "Idler's" mean (on the right hand side of mibbit) 16:08:16 elgar presented TMO at bio-it world 16:08:54 + +33.3.54.95.aadd 16:09:28 Zakim, who is here? 16:09:28 On the phone I see Bob_Powers, +62427aaaa, ??P13, +1.518.276.aabb, ??P4, +46.4.63.3.aacc, +33.3.54.95.aadd 16:09:30 On IRC I see joanne, bbalsa, bobP, matthias_samwald, mscottm, RRSAgent, Zakim, michel, adriencoulet, ericP 16:09:40 Michel: Discussion of paper, more detail about use case 16:09:42 Zakim, +33.3.54.95.aadd is adriencoulet 16:09:42 +adriencoulet; got it 16:09:57 Zakim, +62427aaaa is mscottm 16:09:57 +mscottm; got it 16:10:19 ... Adrian Coulet w. sopharm; We are lucky to have Adrian participate 16:10:23 Zakim, +46.4.63.3.aacc is bbalsa 16:10:23 +bbalsa; got it 16:10:41 thank you ! 16:11:02 ... 1) warfarin 2) breast cancer; 2) let's talk about this story 16:11:49 Scott: Talked w Daniel Rueben(?) and John Madden about bc 16:11:57 Daniel Rubin 16:12:04 ? 16:12:24 ... lots of people understand the terminology involved 16:12:46 ... consider oncoDX and Nanoprint(?) 16:13:14 ... making use of molecular info about patient in order to stratify, to make better choices 16:14:13 ... also discover clinical trials and drugs in development 16:14:24 s/Nanoprint/Mammaprint 16:14:44 ... easily understandable to the audience; reduces costs and needless suffering 16:15:02 OncoDX: http://www.oncotypedx.com/en-US/Breast/HealthcareProfessional/ClinicalSummary.aspx 16:15:07 ... increases patient care. All nice goals for theoretical use cases 16:15:23 Mammaprint: http://www.agendia.com/pages/mammaprint/21.php 16:15:30 ... note that each use case applied to millions of women 16:16:07 ... also clinician-single patient application. Still needs to be implemented in hospital IT 16:16:30 paper: https://docs.google.com/document/d/1lKdDSb2uBBIeTEQAv2CyTHN_aVW63k9si1hmmilOMi0/edit?hl=en&authkey=CJGUtcwF# 16:16:32 Scott: I wrote a few things in 16:17:22 ... not sitting on bc data, but we do have some kidney transplant data. 16:17:45 ... might be able to get some data from Mammaprint people 16:18:16 Joanne: Data are critical; any public bc datasets? 16:18:26 ... can bring in IO too 16:18:47 Scott - breaking up! 16:19:32 Scott: ... data did not have info, embedded in a giant object model 16:19:54 ... dropped effort b/c did not want to parse thru it all. 16:20:33 ... working w theoretical scenarios, hardest challenge is to come up w realistic gx profile 16:20:55 ... nobody reading article will need to look at differential expression 16:21:10 ... we are putting forth a proof-of-concept 16:21:22 ... but, true, the more realistic the better 16:21:47 http://www.pharmgkb.org/do/serve?objId=PA443560&objCls=Disease#tabview=tab6 16:22:00 some PGx about breast neoplasms 16:22:38 Joanne: Knows group w/in Zach's dept 16:23:01 ... Ponolacco(?) 16:23:38 Michel: Adrian has posted this link w. data 16:23:48 -adriencoulet 16:24:00 thanks Adrien! 16:24:13 We lost Adrian 16:24:52 Peter Tonellato 16:25:08 +adriencoulet 16:25:29 Michel: Shows down to alleles 16:26:03 ... mostly tamoxifen datasets 16:26:05 All: when you aren't speaking, please mute (it should help us to get rid of the echo) 16:26:47 Web Site for Peter Tonellato's group: http://lpm.hms.harvard.edu/ 16:27:41 Michel: #7 looks good! Joanne agrees 16:28:09 http://www.pharmgkb.org/do/serve?objId=PA646603&objCls=PhenotypeDataset#tabview=tab2 16:28:53 Males do get bc. 16:31:38 Michel: Cool w. alleles, but no outcomes here. Need to read the paper to understand remission 16:32:36 ... convert to RDF, then query? 16:33:10 ... these are the actual data; Not been formalized to RDF yet. 16:33:29 ... will require some significant curation. Columnn headers require some work. 16:34:09 ... base change definitions, we will have to parse this on a case-by-case basis 16:34:37 Matthias: commenting here 16:34:54 Joanne will develop use cases 16:35:32 Michel: Need to download the data and parse 16:36:04 e.g., http://www.snpedia.com/index.php/CYP3A5 lists the allele names (*1, *5 etc.), but unfortunately not in a way that would make it show up in the current RDF version of SNPedia. 16:36:17 Joanne: TMO or separate ontology? 16:37:00 Matthias: Started ont, tried to align everything w TMO and other authorities 16:37:22 ... raw at the moment. Want to use it for clinical decision support 16:38:23 Scott: Do you have use cases? Interviewing clinician? 16:38:40 Matthias: Blue sky research at the moment. 16:39:31 Univ. of Nancy 16:40:17 Adrian: PhD pharmacogenomics text mining 16:40:49 Adrien: Prof at Univ of Nancy, did PhD with PharmGKB, from Mark Musen's lab (just returned from NCBO to France) 16:41:18 Adrien recently published work on SO-Pharm 16:41:24 Michel: Submit 1st week in May(?) 16:41:40 http://www.loria.fr/~coulet/ 16:41:52 ... important to develop use case, as it relates to PharmGKB website 16:44:15 Scott: Maybe hook up w Terminology call 16:46:42 https://docs.google.com/drawings/edit?id=1OaqlmiTbIAkgHM6kCV-4xbRddHJiN1YZkCWdNHvwiGI&hl=en&authkey=CIT4rcwM 16:47:11 Michel: Look at diagram, a general model in advance of use case 16:49:15 ... ontology would be purple boxes 16:52:21 Matthias asking about gene variant as attribute of population and not of person 16:53:07 Scott: Better to have sample population associated w gene frequency 16:53:30 i have to leave now. Would someone volunteer to contact me later and be willing to go over the diagram with me - preferably tomorrow? Michel, ideally, but if you can't someone else who understands it as well (not having generated) 16:53:35 ... (Scott was asking here...) 16:53:47 bye. 16:53:53 Matthias: Arrow from freq to pop? 16:53:54 bye :) 16:54:25 Michel: Gene variant is still part of an individual 16:54:40 - +1.518.276.aabb 16:54:43 ... to assoc freq, has to be a sub-type 16:54:51 -adriencoulet 16:55:42 +adriencoulet 16:55:47 ... variant in population is a sub-class of variant in individual(?), has more property restriction 16:56:15 Matthias: In my view, it's not really a subclass 16:56:40 Scott: One class of snp, diff freqs of measurement in different population 16:57:19 Michel: But we do assign(?) these genes to specific individuals 16:58:21 Scott: We could have a number of models; test would be how to find w owl or sparql 16:58:43 ... demonstate the differences of how the different models work 16:59:15 ... brca1 has certain freq in pop, but fewer known alleles which are known to be associated w cancer 16:59:35 ... compared to snps which are known to be associated w cancer 16:59:51 ... gwas might have millions of snps to go thru for genome 17:00:06 ... brca measure is more like a read-out of a prognosis. 17:00:26 ... Carry out further w. email exchange. 17:00:48 Michel: Add this discussion to the paper 17:01:39 -??P4 17:01:39 -Bob_Powers 17:01:41 -bbalsa 17:01:42 Scott was actually saying that the BRCA1 allele is directly associated with a type of cancer. 17:01:43 -??P13 17:01:50 -adriencoulet 17:02:11 rrsagent, draft minutes 17:02:11 I have made the request to generate http://www.w3.org/2011/04/14-hcls2-minutes.html michel 17:02:18 whereas you might have millions of SNPs, very few SNP combinations are directly associated with a cancer outcome 17:02:19 rrsagent, make log world-visible 17:02:57 -mscottm 17:02:59 SW_HCLS(TMO)11:00AM has ended 17:03:01 Attendees were Bob_Powers, +1.518.276.aabb, adriencoulet, mscottm, bbalsa 18:02:47 david_r_newman has joined #hcls2 18:18:11 Zakim has left #hcls2