- From: mdmiller <mdmiller53@comcast.net>
- Date: Wed, 26 May 2010 06:41:12 -0700
- To: "Kei Cheung" <kei.cheung@yale.edu>
- Cc: "HCLS" <public-semweb-lifesci@w3.org>
hi kei, > What do we mean by differentially expressed genes? One definition is that > differentially expressed genes are genes with significantly different > expression in two samples/conditions/experimental factors/dimensions > (e.g., treated vs. untreated, disease vs, normal, time point1 vs. time > point 2) of microarray experiments. yes, this was my meaning. this is to differentiate between a gene that is always expressed under normal conditions because it is part of an essential pathway that is always running, that gene is only interesting if its expression level changes--similarly for a normally unexpressed gene. > How to measure or infer gene expression (e.g., from mRNA) is a whole > complex question that may be beyond the scope of our use case. yes, which i think was scott's point in his reply. in fact, for the BioRDF use case, initially at least, it is probably sufficient that the authors of the paper state that a gene is part of the significant gene list. cheers, michael ----- Original Message ----- From: "Kei Cheung" <kei.cheung@yale.edu> To: "mdmiller" <mdmiller53@comcast.net> Cc: "M. Scott Marshall" <marshall@science.uva.nl>; "HCLS" <public-semweb-lifesci@w3.org> Sent: Tuesday, May 25, 2010 8:52 PM Subject: Re: BioRDF Telcon > Hi Michael et al, > > What do we mean by differentially expressed genes? One definition is that > differentially expressed genes are genes with significantly different > expression in two samples/conditions/experimental factors/dimensions > (e.g., treated vs. untreated, disease vs, normal, time point1 vs. time > point 2) of microarray experiments. > > How to measure or infer gene expression (e.g., from mRNA) is a whole > complex question that may be beyond the scope of our use case. > > Cheers, > > -Kei > > mdmiller wrote: > >> hi scott, >> >> i think you, jim and lena are doing a great job moving the technical >> aspect of this work forward. i'm looking forward to seeing the end >> results. >> >> cheers, >> michael >> >> ----- Original Message ----- From: "M. Scott Marshall" >> <marshall@science.uva.nl> >> To: "mdmiller" <mdmiller53@comcast.net> >> Cc: "Kei Cheung" <kei.cheung@yale.edu>; "HCLS" >> <public-semweb-lifesci@w3.org> >> Sent: Tuesday, May 25, 2010 10:21 AM >> Subject: Re: BioRDF Telcon >> >> >>> Hi Michael, >>> >>> Thanks for the clarification. I also explained those concepts during >>> the BioRDF teleconference but it is difficult for the scribe to >>> capture such details accurately from a phone conversation. Just >>> knowing that a gene has changed (either up or down) already gives us >>> something to work with. Since we started with the microarray use case, >>> we have aimed to focus on the list of differentially expressed genes >>> as our entry point into related molecular information, phenotypes, >>> pathways, diseases, etc. >>> >>> In addition to the gene list and experimental factors, there is some >>> data provenance information that characterizes the origins of the gene >>> list, such as the type of significant analysis or technique that was >>> performed (ANOVA, LIMMA, ..) and p-value cutoff for the list discussed >>> in the associated article(s), software packages used (specific R >>> package from BioConductor, GeneSpring, NextBio, ..). It would be handy >>> if there was a common vocabulary for this type of information (URI's >>> for statistical techniques and software packages). I think that some >>> related resources have been described by myGrid/myExperiment. However, >>> lacking a complete vocabulary, it is still possible to make use of the >>> gene list without such a fine grained description of its provenance. >>> >>> Cheers, >>> Scott >>> >>> On Tue, May 25, 2010 at 9:35 AM, mdmiller <mdmiller53@comcast.net> >>> wrote: >>> >>>> hi all, >>>> >>>> sorry i ended up not being able to make the call. >>>> >>>> "P value >>>> The probability (ranging from zero to one) that the results observed in >>>> a >>>> study could have occurred by chance if the null hypothesis was true. A >>>> P >>>> value of ? 0.05 is often used as a threshold to indicate statistical >>>> significance." (1) >>>> >>>> the exact meaning of p-value depends on what is being measured. >>>> >>>> also, sometimes it isn't so important that a gene is up or down >>>> regulated >>>> but whether its expression changes from up or down regulated over the >>>> experimental factors, e.g. if you increase the dose of the drug do the >>>> target genes go from non-expressed to up regulated. >>>> >>>> cheers, >>>> michael >>>> >>>> 1) >>>> http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=antiepi&part=appendixes.app2 >>>> >>>> ----- Original Message ----- From: "Kei Cheung" <kei.cheung@yale.edu> >>>> To: "HCLS" <public-semweb-lifesci@w3.org> >>>> Sent: Monday, May 24, 2010 11:40 AM >>>> Subject: Re: BioRDF Telcon >>>> >>>> >>>>> Today's minutes are available at: >>>>> >>>>> >>>>> http://esw.w3.org/HCLSIG_BioRDF_Subgroup/Meetings/2010/05-24_Conference_Call >>>>> >>>>> Thanks to Matthias for scribing. >>>>> >>>>> Cheers, >>>>> >>>>> -Kei >>>>> >>>>> mdmiller wrote: >>>>> >>>>>> >>>>>> hi kei, >>>>>> >>>>>> look forward to joining the call, >>>>>> michael >>>>>> >>>>>> ----- Original Message ----- From: "Kei Cheung" <kei.cheung@yale.edu> >>>>>> To: "mdmiller" <mdmiller53@comcast.net>; "HCLS" >>>>>> <public-semweb-lifesci@w3.org> >>>>>> Sent: Saturday, May 22, 2010 12:10 PM >>>>>> Subject: Re: BioRDF Telcon >>>>>> >>>>>> >>>>>>> Hi Michael, >>>>>>> >>>>>>> Yes, May 24 was what I meant. It was a typo. >>>>>>> >>>>>>> Thanks, >>>>>>> >>>>>>> -Kei >>>>>>> >>>>>>> mdmiller wrote: >>>>>>> >>>>>>>> hi kei, >>>>>>>> >>>>>>>> do you mean monday (may 24)? >>>>>>>> >>>>>>>> cheers, >>>>>>>> michael >>>>>>>> >>>>>>>> ----- Original Message ----- From: "Kei Cheung" >>>>>>>> <kei.cheung@yale.edu> >>>>>>>> To: "JunZhao" <jun.zhao@zoo.ox.ac.uk> >>>>>>>> Cc: <public-semweb-lifesci@w3.org> >>>>>>>> Sent: Friday, May 21, 2010 2:28 PM >>>>>>>> Subject: Re: BioRDF Telcon >>>>>>>> >>>>>>>> >>>>>>>>> Since there were only Jun and Scott who attended the last BioRDF >>>>>>>>> call >>>>>>>>> (I was not able to attend due to some emergency meetings), we >>>>>>>>> decided to >>>>>>>>> have the next BioRDF call on the coming Monday (May 21) at 11 am >>>>>>>>> (EDT). The >>>>>>>>> agenda will be the same (see below). >>>>>>>>> >>>>>>>>> Cheers, >>>>>>>>> >>>>>>>>> -Kei >>>>>>>>> >>>>>>>>> JunZhao wrote: >>>>>>>>> >>>>>>>>>> This is a reminder that the next BioRDF telcon call will be held >>>>>>>>>> at >>>>>>>>>> 11 >>>>>>>>>> am EDT (4 pm CET) on Monday, May 17 (see details below). >>>>>>>>>> >>>>>>>>>> Cheers, >>>>>>>>>> >>>>>>>>>> -Jun >>>>>>>>>> >>>>>>>>>> >>>>>>>>>> == Conference Details == >>>>>>>>>> * Date of Call: Monday, May 17, 2010 >>>>>>>>>> * Time of Call: 11:00 am Eastern Time (4 pm CET) >>>>>>>>>> * Dial-In #: +1.617.761.6200 (Cambridge, MA) >>>>>>>>>> * Dial-In #: +33.4.89.06.34.99 (Nice, France) >>>>>>>>>> * Dial-In #: +44.117.370.6152 (Bristol, UK) >>>>>>>>>> * Participant Access Code: 4257 ("HCLS") >>>>>>>>>> * IRC Channel: irc.w3.org port 6665 channel #HCLS (see W3C IRC >>>>>>>>>> page >>>>>>>>>> for >>>>>>>>>> details, or see Web IRC), Quick Start: Use >>>>>>>>>> http://www.mibbit.com/chat/?server=irc.w3.org:6665&channel=%23hcls >>>>>>>>>> for >>>>>>>>>> IRC access. >>>>>>>>>> * Duration: ~1 hour >>>>>>>>>> * Frequency: bi-weekly >>>>>>>>>> * Convener: Jun >>>>>>>>>> * Scribe: to-be-determined >>>>>>>>>> >>>>>>>>>> ==Agenda== >>>>>>>>>> * Introduction >>>>>>>>>> * Gene list RDF representation >>>>>>>>>> * iPhone demo >>>>>>>>>> >>>>>>>>>> >>>>>>>>> >>>>>>>>> >>>>>>>>> >>>>>>>> >>>>>>> >>>>>>> >>>>>> >>>>>> >>>>>> >>>>> >>>>> >>>>> >>>> >>>> >>>> >>>> >>> >> >> >> > >
Received on Wednesday, 26 May 2010 13:41:56 UTC