GO graph plotting with some in color
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Loren Engrav ★ 1.0k
@loren-engrav-2040
Last seen 9.6 years ago
So am doing GO graphing and I have done > bpCutLeaves <- scan(file="343afterDupesNotCut.txt", what = "character") Read 343 items > bpCutLeavestree <- GOGraph(bpCutLeaves, GOBPPARENTS) > postscript ("bpCutLeavestreeTest.ps", width=100, height = 100, paper="special"); plot (bpCutLeavestree); dev.off() quartz 2 > bpCutLeavestree A graphNEL graph with directed edges Number of Nodes = 1456 Number of Edges = 2418 And the postscript file is very nice But I need the 343 leaves colored red (over expression) and blue (under expression) So from Rgraphviz documentation I do > nAttrs <- list() > nAttrs$color <- scan(file="343forColorBB.txt", what="character") Read 343 items > nAttrs$fillcolor <- scan(file="343forColorBB.txt", what="character") Read 343 items Where in 343ForColorBB.txt I set the 343 to red or blue, it is a text file with 343 items like GO:0000002="red" Then I do > postscript ("bpCutLeavestreeTest.ps", width=100, height = 100, paper="special"); plot (bpCutLeavestree, nodeAttrs = nAttrs); dev.off() But it returns Error in buildNodeList(graph, nodeAttrs, subGList, attrs$node) : the character vector must have names I am stuck... What have I left out Thank you Loren Engrav Univ Wash Seattle
GO graph Rgraphviz GO graph Rgraphviz • 1.0k views
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Loren Engrav ★ 1.0k
@loren-engrav-2040
Last seen 9.6 years ago
Followup to this issue I can move the color data from Excel to BBedit Then edit till I have the string like GO:0004198="red", GO:004199="blue" Then copy paste into the c function and the error below does not occur and I obtain red and blue nodes, which is cool This may be good enough. But can I set up a text file in some form and then read or scan or something the data in? I have tried scan and read.delim and googled, etc but have failed Thank you ========================================= > From: Loren Engrav <engrav at="" u.washington.edu=""> > Date: Fri, 23 Nov 2007 13:31:32 -0800 > To: <bioconductor at="" stat.math.ethz.ch=""> > Conversation: GO graph plotting with some in color > Subject: [BioC] GO graph plotting with some in color > > > So am doing GO graphing and I have done > >> bpCutLeaves <- scan(file="343afterDupesNotCut.txt", what = "character") > Read 343 items >> bpCutLeavestree <- GOGraph(bpCutLeaves, GOBPPARENTS) >> postscript ("bpCutLeavestreeTest.ps", width=100, height = 100, > paper="special"); plot (bpCutLeavestree); dev.off() > quartz > 2 >> bpCutLeavestree > A graphNEL graph with directed edges > Number of Nodes = 1456 > Number of Edges = 2418 > > And the postscript file is very nice > But I need the 343 leaves colored red (over expression) and blue (under > expression) > > So from Rgraphviz documentation I do > >> nAttrs <- list() >> nAttrs$color <- scan(file="343forColorBB.txt", what="character") > Read 343 items >> nAttrs$fillcolor <- scan(file="343forColorBB.txt", what="character") > Read 343 items > > Where in 343ForColorBB.txt I set the 343 to red or blue, it is a text file > with 343 items like GO:0000002="red" > > Then I do >> postscript ("bpCutLeavestreeTest.ps", width=100, height = 100, > paper="special"); plot (bpCutLeavestree, nodeAttrs = nAttrs); dev.off() > > But it returns > > Error in buildNodeList(graph, nodeAttrs, subGList, attrs$node) : > the character vector must have names > > I am stuck... > What have I left out > > Thank you > > Loren Engrav > Univ Wash > Seattle > > _______________________________________________ > Bioconductor mailing list > Bioconductor at stat.math.ethz.ch > https://stat.ethz.ch/mailman/listinfo/bioconductor > Search the archives: > http://news.gmane.org/gmane.science.biology.informatics.conductor
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Loren Engrav wrote: > Followup to this issue > > I can move the color data from Excel to BBedit > Then edit till I have the string like GO:0004198="red", GO:004199="blue" > Then copy paste into the c function and the error below does not occur and I > obtain red and blue nodes, which is cool If you read the documentation for the function you are trying to use, it will explain the format of the arguments. In this case you need a named vector. You can also evaluate the examples and see what was used to create them. If you then look at what you get when you read in the data from a file, as you have described, you will see it is not a named vector, and you will need to process it to get the form needed to pass on to the plotting routines. Perhaps the easiest way is to replace the = in your file with a comma or some other delimiter (or use the sep argument in the read.table/read.delim family of functions - lots of documentation here too, ?read.delim) and read in the data as a data.frame. Then use that to create the named vector. > > This may be good enough. But can I set up a text file in some form and then > read or scan or something the data in? > > I have tried scan and read.delim and googled, etc but have failed > > Thank you > ========================================= > >> From: Loren Engrav <engrav at="" u.washington.edu=""> >> Date: Fri, 23 Nov 2007 13:31:32 -0800 >> To: <bioconductor at="" stat.math.ethz.ch=""> >> Conversation: GO graph plotting with some in color >> Subject: [BioC] GO graph plotting with some in color >> >> >> So am doing GO graphing and I have done >> >>> bpCutLeaves <- scan(file="343afterDupesNotCut.txt", what = "character") >> Read 343 items >>> bpCutLeavestree <- GOGraph(bpCutLeaves, GOBPPARENTS) >>> postscript ("bpCutLeavestreeTest.ps", width=100, height = 100, >> paper="special"); plot (bpCutLeavestree); dev.off() >> quartz >> 2 >>> bpCutLeavestree >> A graphNEL graph with directed edges >> Number of Nodes = 1456 >> Number of Edges = 2418 >> >> And the postscript file is very nice >> But I need the 343 leaves colored red (over expression) and blue (under >> expression) >> >> So from Rgraphviz documentation I do >> >>> nAttrs <- list() >>> nAttrs$color <- scan(file="343forColorBB.txt", what="character") >> Read 343 items >>> nAttrs$fillcolor <- scan(file="343forColorBB.txt", what="character") >> Read 343 items >> >> Where in 343ForColorBB.txt I set the 343 to red or blue, it is a text file >> with 343 items like GO:0000002="red" >> >> Then I do >>> postscript ("bpCutLeavestreeTest.ps", width=100, height = 100, >> paper="special"); plot (bpCutLeavestree, nodeAttrs = nAttrs); dev.off() >> >> But it returns >> >> Error in buildNodeList(graph, nodeAttrs, subGList, attrs$node) : >> the character vector must have names >> >> I am stuck... >> What have I left out >> >> Thank you >> >> Loren Engrav >> Univ Wash >> Seattle >> >> _______________________________________________ >> Bioconductor mailing list >> Bioconductor at stat.math.ethz.ch >> https://stat.ethz.ch/mailman/listinfo/bioconductor >> Search the archives: >> http://news.gmane.org/gmane.science.biology.informatics.conductor > > _______________________________________________ > Bioconductor mailing list > Bioconductor at stat.math.ethz.ch > https://stat.ethz.ch/mailman/listinfo/bioconductor > Search the archives: http://news.gmane.org/gmane.science.biology.informatics.conductor > -- Robert Gentleman, PhD Program in Computational Biology Division of Public Health Sciences Fred Hutchinson Cancer Research Center 1100 Fairview Ave. N, M2-B876 PO Box 19024 Seattle, Washington 98109-1024 206-667-7700 rgentlem at fhcrc.org
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Cool, thank you After 11 days I can read in the data and have the graph That is a rather expensive graph I would say :) > nAttrs = list() > colors <- scan(file="339colorsRowBB.txt", what="character") Read 339 items > names(colors) <- scan(file="339namesRowBB.txt", what="character") Read 339 items > nAttrs$fillcolor <- colors > nAttrs$color <- colors > bpCutLeaves <- scan(file="339namesRowBB.txt", what = "character") Read 339 items > bpCutLeavestree <- GOGraph(bpCutLeaves, GOBPPARENTS) > postscript ("bpCutLeavestree.ps", width=100, height = 100, paper="special"); plot (bpCutLeavestree, nodeAttrs=nAttrs); dev.off() postscript 2 Graph is up at <http: homepage.mac.com="" engrav="" menu9.html=""> and hit arrow on FileSharing Now I have 3 questions please 1) the code above reads in two files, one for colors and one for names; that seems rather grade school, is there not a more efficient way, like with one file 2) in the graph the colored and therefore "significant" nodes have no incoming edges from other colored and "significant" nodes; is it possible that none of the 339 "significant" nodes have a parent within the 339? 3) and finally, What do I have? We are getting enrichment from DAVID and Amigo as they are lots more user friendly than Bioconductor. But they fail at plotting so I tried Bioconductor. The resultant graph shows red and blue sprinkled here and there but so what? I found a manuscript with an almost identical graph with credits to Bioconductor. See Journal of Molecular Endocrinology (2006) 37, 301?316. I checked their conclusions from the graph and found them rather skimpy. What is the conclusion from the graph? Or is it just a pretty graph? But it was fun, by the way. Again thank you for helping. I am grateful. Loren Engrav Univ Wash Seattle, WA USA > From: Robert Gentleman <rgentlem at="" fhcrc.org=""> > Date: Mon, 26 Nov 2007 11:33:58 -0800 > To: Loren Engrav <engrav at="" u.washington.edu=""> > Cc: <bioconductor at="" stat.math.ethz.ch=""> > Subject: Re: [BioC] GO graph plotting with some in color > > > > Loren Engrav wrote: >> Followup to this issue >> >> I can move the color data from Excel to BBedit >> Then edit till I have the string like GO:0004198="red", GO:004199="blue" >> Then copy paste into the c function and the error below does not occur and I >> obtain red and blue nodes, which is cool > > If you read the documentation for the function you are trying to use, > it will explain the format of the arguments. In this case you need a > named vector. You can also evaluate the examples and see what was used > to create them. > > If you then look at what you get when you read in the data from a > file, as you have described, you will see it is not a named vector, and > you will need to process it to get the form needed to pass on to the > plotting routines. > > Perhaps the easiest way is to replace the = in your file with a comma > or some other delimiter (or use the sep argument in the > read.table/read.delim family of functions - lots of documentation here > too, ?read.delim) and read in the data as a data.frame. Then use that to > create the named vector. > > >> >> This may be good enough. But can I set up a text file in some form and then >> read or scan or something the data in? >> >> I have tried scan and read.delim and googled, etc but have failed >> >> Thank you >> ========================================= >> >>> From: Loren Engrav <engrav at="" u.washington.edu=""> >>> Date: Fri, 23 Nov 2007 13:31:32 -0800 >>> To: <bioconductor at="" stat.math.ethz.ch=""> >>> Conversation: GO graph plotting with some in color >>> Subject: [BioC] GO graph plotting with some in color >>> >>> >>> So am doing GO graphing and I have done >>> >>>> bpCutLeaves <- scan(file="343afterDupesNotCut.txt", what = "character") >>> Read 343 items >>>> bpCutLeavestree <- GOGraph(bpCutLeaves, GOBPPARENTS) >>>> postscript ("bpCutLeavestreeTest.ps", width=100, height = 100, >>> paper="special"); plot (bpCutLeavestree); dev.off() >>> quartz >>> 2 >>>> bpCutLeavestree >>> A graphNEL graph with directed edges >>> Number of Nodes = 1456 >>> Number of Edges = 2418 >>> >>> And the postscript file is very nice >>> But I need the 343 leaves colored red (over expression) and blue (under >>> expression) >>> >>> So from Rgraphviz documentation I do >>> >>>> nAttrs <- list() >>>> nAttrs$color <- scan(file="343forColorBB.txt", what="character") >>> Read 343 items >>>> nAttrs$fillcolor <- scan(file="343forColorBB.txt", what="character") >>> Read 343 items >>> >>> Where in 343ForColorBB.txt I set the 343 to red or blue, it is a text file >>> with 343 items like GO:0000002="red" >>> >>> Then I do >>>> postscript ("bpCutLeavestreeTest.ps", width=100, height = 100, >>> paper="special"); plot (bpCutLeavestree, nodeAttrs = nAttrs); dev.off() >>> >>> But it returns >>> >>> Error in buildNodeList(graph, nodeAttrs, subGList, attrs$node) : >>> the character vector must have names >>> >>> I am stuck... >>> What have I left out >>> >>> Thank you >>> >>> Loren Engrav >>> Univ Wash >>> Seattle >>> >>> _______________________________________________ >>> Bioconductor mailing list >>> Bioconductor at stat.math.ethz.ch >>> https://stat.ethz.ch/mailman/listinfo/bioconductor >>> Search the archives: >>> http://news.gmane.org/gmane.science.biology.informatics.conductor >> >> _______________________________________________ >> Bioconductor mailing list >> Bioconductor at stat.math.ethz.ch >> https://stat.ethz.ch/mailman/listinfo/bioconductor >> Search the archives: >> http://news.gmane.org/gmane.science.biology.informatics.conductor >> > > -- > Robert Gentleman, PhD > Program in Computational Biology > Division of Public Health Sciences > Fred Hutchinson Cancer Research Center > 1100 Fairview Ave. N, M2-B876 > PO Box 19024 > Seattle, Washington 98109-1024 > 206-667-7700 > rgentlem at fhcrc.org
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Loren Engrav wrote: > Cool, thank you > > After 11 days > I can read in the data and have the graph > That is a rather expensive graph I would say :) It depends a lot on what your options were, I suspect as compared to something like Ingenuity it was a remarkably cheap graph, but you might investigate that option. There are lots of commercial vendors that would love to sell you something. > >> nAttrs = list() >> colors <- scan(file="339colorsRowBB.txt", what="character") > Read 339 items >> names(colors) <- scan(file="339namesRowBB.txt", what="character") > Read 339 items >> nAttrs$fillcolor <- colors >> nAttrs$color <- colors > >> bpCutLeaves <- scan(file="339namesRowBB.txt", what = "character") > Read 339 items >> bpCutLeavestree <- GOGraph(bpCutLeaves, GOBPPARENTS) >> postscript ("bpCutLeavestree.ps", width=100, height = 100, paper="special"); > plot (bpCutLeavestree, nodeAttrs=nAttrs); dev.off() > postscript > 2 > > > Graph is up at <http: homepage.mac.com="" engrav="" menu9.html=""> and hit arrow on > FileSharing > > Now I have 3 questions please > > 1) the code above reads in two files, one for colors and one for names; that > seems rather grade school, is there not a more efficient way, like with one > file Yes, put them all in one comma (or otherwise separated) file and read that in, with read.table, or something like that, and then manipulate in R. > > 2) in the graph the colored and therefore "significant" nodes have no > incoming edges from other colored and "significant" nodes; is it possible > that none of the 339 "significant" nodes have a parent within the 339? It depends on what you did, and you do seem to really insist on not giving details, so I am not sure what to say. If you used the conditional test then the point of conditioning is to remove the parent-child artifact. For complete details you need to read either our paper or Adrian Alexa's, references given in another thread today. > > 3) and finally, What do I have? We are getting enrichment from DAVID and > Amigo as they are lots more user friendly than Bioconductor. But they fail > at plotting so I tried Bioconductor. The resultant graph shows red and blue > sprinkled here and there but so what? Computing something is no substitute for understanding it. It is not easy to help here, as one would need to know what your scientific objectives are and how using GO, or other functional information might help to achieve those objectives. These are tools that can be used for many purposes, and do require some non-trivial interpretation. UW has a good Biostatistics Dept, consulting someone there is probably your best bet. > > I found a manuscript with an almost identical graph with credits to > Bioconductor. See Journal of Molecular Endocrinology (2006) 37, 301?316. I > checked their conclusions from the graph and found them rather skimpy. > > What is the conclusion from the graph? Or is it just a pretty graph? But it > was fun, by the way. > > Again thank you for helping. I am grateful. you're welcome > > Loren Engrav > Univ Wash > Seattle, WA USA > > >> From: Robert Gentleman <rgentlem at="" fhcrc.org=""> >> Date: Mon, 26 Nov 2007 11:33:58 -0800 >> To: Loren Engrav <engrav at="" u.washington.edu=""> >> Cc: <bioconductor at="" stat.math.ethz.ch=""> >> Subject: Re: [BioC] GO graph plotting with some in color >> >> >> >> Loren Engrav wrote: >>> Followup to this issue >>> >>> I can move the color data from Excel to BBedit >>> Then edit till I have the string like GO:0004198="red", GO:004199="blue" >>> Then copy paste into the c function and the error below does not occur and I >>> obtain red and blue nodes, which is cool >> If you read the documentation for the function you are trying to use, >> it will explain the format of the arguments. In this case you need a >> named vector. You can also evaluate the examples and see what was used >> to create them. >> >> If you then look at what you get when you read in the data from a >> file, as you have described, you will see it is not a named vector, and >> you will need to process it to get the form needed to pass on to the >> plotting routines. >> >> Perhaps the easiest way is to replace the = in your file with a comma >> or some other delimiter (or use the sep argument in the >> read.table/read.delim family of functions - lots of documentation here >> too, ?read.delim) and read in the data as a data.frame. Then use that to >> create the named vector. >> >> >>> This may be good enough. But can I set up a text file in some form and then >>> read or scan or something the data in? >>> >>> I have tried scan and read.delim and googled, etc but have failed >>> >>> Thank you >>> ========================================= >>> >>>> From: Loren Engrav <engrav at="" u.washington.edu=""> >>>> Date: Fri, 23 Nov 2007 13:31:32 -0800 >>>> To: <bioconductor at="" stat.math.ethz.ch=""> >>>> Conversation: GO graph plotting with some in color >>>> Subject: [BioC] GO graph plotting with some in color >>>> >>>> >>>> So am doing GO graphing and I have done >>>> >>>>> bpCutLeaves <- scan(file="343afterDupesNotCut.txt", what = "character") >>>> Read 343 items >>>>> bpCutLeavestree <- GOGraph(bpCutLeaves, GOBPPARENTS) >>>>> postscript ("bpCutLeavestreeTest.ps", width=100, height = 100, >>>> paper="special"); plot (bpCutLeavestree); dev.off() >>>> quartz >>>> 2 >>>>> bpCutLeavestree >>>> A graphNEL graph with directed edges >>>> Number of Nodes = 1456 >>>> Number of Edges = 2418 >>>> >>>> And the postscript file is very nice >>>> But I need the 343 leaves colored red (over expression) and blue (under >>>> expression) >>>> >>>> So from Rgraphviz documentation I do >>>> >>>>> nAttrs <- list() >>>>> nAttrs$color <- scan(file="343forColorBB.txt", what="character") >>>> Read 343 items >>>>> nAttrs$fillcolor <- scan(file="343forColorBB.txt", what="character") >>>> Read 343 items >>>> >>>> Where in 343ForColorBB.txt I set the 343 to red or blue, it is a text file >>>> with 343 items like GO:0000002="red" >>>> >>>> Then I do >>>>> postscript ("bpCutLeavestreeTest.ps", width=100, height = 100, >>>> paper="special"); plot (bpCutLeavestree, nodeAttrs = nAttrs); dev.off() >>>> >>>> But it returns >>>> >>>> Error in buildNodeList(graph, nodeAttrs, subGList, attrs$node) : >>>> the character vector must have names >>>> >>>> I am stuck... >>>> What have I left out >>>> >>>> Thank you >>>> >>>> Loren Engrav >>>> Univ Wash >>>> Seattle >>>> >>>> _______________________________________________ >>>> Bioconductor mailing list >>>> Bioconductor at stat.math.ethz.ch >>>> https://stat.ethz.ch/mailman/listinfo/bioconductor >>>> Search the archives: >>>> http://news.gmane.org/gmane.science.biology.informatics.conductor >>> _______________________________________________ >>> Bioconductor mailing list >>> Bioconductor at stat.math.ethz.ch >>> https://stat.ethz.ch/mailman/listinfo/bioconductor >>> Search the archives: >>> http://news.gmane.org/gmane.science.biology.informatics.conductor >>> >> -- >> Robert Gentleman, PhD >> Program in Computational Biology >> Division of Public Health Sciences >> Fred Hutchinson Cancer Research Center >> 1100 Fairview Ave. N, M2-B876 >> PO Box 19024 >> Seattle, Washington 98109-1024 >> 206-667-7700 >> rgentlem at fhcrc.org > > _______________________________________________ > Bioconductor mailing list > Bioconductor at stat.math.ethz.ch > https://stat.ethz.ch/mailman/listinfo/bioconductor > Search the archives: http://news.gmane.org/gmane.science.biology.informatics.conductor > -- Robert Gentleman, PhD Program in Computational Biology Division of Public Health Sciences Fred Hutchinson Cancer Research Center 1100 Fairview Ave. N, M2-B876 PO Box 19024 Seattle, Washington 98109-1024 206-667-7700 rgentlem at fhcrc.org
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Thank you again for discussing, I am grateful Cost? True, Ingenuity is like $8,000 per year and does not make graphs as I can see, I examined Genesifter Genespring GoMiner and Gene_xyz and returned to Bio, and the others would all love to sell something, is true, most certainly Still, 12 days for one graph is expensive R and Bioconductor are not easy to use for the beginner Like I did > rows2 <- read.delim(file="339namesColorsRowsBBtab.txt", sep="\t") And the process turned ":" into "." which of course wiped out the GO terms which read like GO:1111111, and it took perhaps an hour to learn to add check.names=FALSE, but so for the novice Question 1....................... Read as one??? Ok with > rows2 <- read.delim(file="339namesColorsRowsBBtab.txt", sep="\t", check.names = FALSE) > colors <- as.matrix(rows2)[1,] I can now read from one file, still two commands but is more fun I found the as.matrix trick in an old email from Brian Ripley in 2004 which is still findable by google So question 1 is done, thank you Question 2................................ As for details, I copied the code exactly from R, that is exactly what I did, no more, no less, I am trying to comply with the detail issue, believe me Or perhaps you mean experimental details. We have Duroc pigs which make thick scar. And Yorkshire pigs that make thin scar. And would like to know why Durocs make thick and perhaps how to alter this. So we wounded the pigs and biopsied them at 1 2 3 12 and 20 weeks. And amplified the RNA and hybridized Affy porcine chips. Then with Bio packages did mixed linear regression and chose to go further with those probes with appropriate p-value. Then cut those probes for which the bio replicates did not match. Then cut those probes for which fold change was <1.4. Then cut those probes for which the Affy present absent calls were illogical. Then cut those probes that do not match human hypertrophic scar since we do not wish to study a pig gene that makes a curly tail. And are left with 1,019 probes of interest. Some of these are dupes so we are down to 953 genes that satisfied all the criteria. And enrichment is likely to come from DAVID but a graph seemed cool so we did makeGoGraph and after study founds many GO terms not relevant and cut them so am now down to 333 "relevant" terms. And continue with the graphing process. Read two papers??? I did, and as you might anticipate they are shall we say "over my head". But I think I am not trying to determine over or under representation at this point. Just make a graph demonstrating where the 333 are located in the "universe" of BPPARENTS with incoming and outgoing edges. But then, maybe that is simply a dumb thing to do. But if not, then question 2, why in the plot do none of the 333 have incoming edges? Is it possible that none of the 333 is a parent to another of the 333? I think I have answered this. If I pick a known ancestor, and put it in the "interesting" file, it appears colored. So would appear none of the 333 have an ancestor within the 333. Interesting. So this is a graph merged from 333 graphs. This then would suggest that any node, colored or not, with lots of incoming edges becomes interesting. Question 3................. So statistics and enrichment I think are not our issue at the moment. So question3 remains. If we would obtain a graph as mentioned with incoming and outgoing edges, would it tell any one anything? Or is enrichment the only deal with GO? Thank again for discussing. I am grateful and appreciative. Thanks again Loren Engrav Univ Wash Seattle > From: Robert Gentleman <rgentlem at="" fhcrc.org=""> > Date: Mon, 26 Nov 2007 17:55:06 -0800 > To: Loren Engrav <engrav at="" u.washington.edu=""> > Cc: <bioconductor at="" stat.math.ethz.ch=""> > Subject: Re: [BioC] GO graph plotting with some in color > > > > Loren Engrav wrote: >> Cool, thank you >> >> After 11 days >> I can read in the data and have the graph >> That is a rather expensive graph I would say :) > > It depends a lot on what your options were, I suspect as compared to > something like Ingenuity it was a remarkably cheap graph, but you might > investigate that option. There are lots of commercial vendors that > would love to sell you something. > >> >>> nAttrs = list() >>> colors <- scan(file="339colorsRowBB.txt", what="character") >> Read 339 items >>> names(colors) <- scan(file="339namesRowBB.txt", what="character") >> Read 339 items >>> nAttrs$fillcolor <- colors >>> nAttrs$color <- colors >> >>> bpCutLeaves <- scan(file="339namesRowBB.txt", what = "character") >> Read 339 items >>> bpCutLeavestree <- GOGraph(bpCutLeaves, GOBPPARENTS) >>> postscript ("bpCutLeavestree.ps", width=100, height = 100, paper="special"); >> plot (bpCutLeavestree, nodeAttrs=nAttrs); dev.off() >> postscript >> 2 >> >> >> Graph is up at <http: homepage.mac.com="" engrav="" menu9.html=""> and hit arrow on >> FileSharing >> >> Now I have 3 questions please >> >> 1) the code above reads in two files, one for colors and one for names; that >> seems rather grade school, is there not a more efficient way, like with one >> file > > Yes, put them all in one comma (or otherwise separated) file and read > that in, with read.table, or something like that, and then manipulate in R. > >> >> 2) in the graph the colored and therefore "significant" nodes have no >> incoming edges from other colored and "significant" nodes; is it possible >> that none of the 339 "significant" nodes have a parent within the 339? > > It depends on what you did, and you do seem to really insist on not > giving details, so I am not sure what to say. If you used the > conditional test then the point of conditioning is to remove the > parent-child artifact. For complete details you need to read either our > paper or Adrian Alexa's, references given in another thread today. > > >> >> 3) and finally, What do I have? We are getting enrichment from DAVID and >> Amigo as they are lots more user friendly than Bioconductor. But they fail >> at plotting so I tried Bioconductor. The resultant graph shows red and blue >> sprinkled here and there but so what? > > Computing something is no substitute for understanding it. It is not > easy to help here, as one would need to know what your scientific > objectives are and how using GO, or other functional information might > help to achieve those objectives. These are tools that can be used for > many purposes, and do require some non-trivial interpretation. UW has a > good Biostatistics Dept, consulting someone there is probably your best bet. > >> >> I found a manuscript with an almost identical graph with credits to >> Bioconductor. See Journal of Molecular Endocrinology (2006) 37, 301?316. I >> checked their conclusions from the graph and found them rather skimpy. >> >> What is the conclusion from the graph? Or is it just a pretty graph? But it >> was fun, by the way. >> >> Again thank you for helping. I am grateful. > > you're welcome > >> >> Loren Engrav >> Univ Wash >> Seattle, WA USA >> >>
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