1,253 results • Page 21 of 21
extdata", "agilent_ID.txt", package="human.db0") >myMeta = c("DBSCHEMA"="HUMANCHIP_DB", "ORGANISM"="Homo sapiens", "SPECIES"="Human", "MANUFACTURER"="Agilent", "CHIPNAME"="Human whole genome 8x60k Array ", "MANUFACTURERURL"="http
<div class="preformatted">Just wondering if anyone has had any luck creating annotation packages for the HTA 2.0 chip? Best, Stephen On Tue, Sep 10, 2013 at 8:24 PM, Mark Cowley <m.cowley@garvan.org.au> wrote: &gt; Hi Vincent &amp; Benilton, &gt; Myself and Philip de Groot have independently tried to create the &gt; pd.hta.2.0.db overnight with the same error (thou…
<div class="preformatted">I'm out of the office until July 28th. Please contact liz higgins if you need assistance @ 636-0163. &gt;&gt;&gt; bioconductor 07/22/06 06:00 &gt;&gt;&gt; Send Bioconductor mailing list submissions to bioconductor at stat.math.ethz.ch To subscribe or unsubscribe via the World Wide Web, visit https://stat.ethz.ch/mailman/li…
<div class="preformatted">Hi Roy- I don't believe these questions ever got answered, we've been very busy! In the first instance, this looks like a good example of a paired experiment, with matched samples for each patient before and after treatment. I'd suggest filling in the "Tissue" field with the patient ID, so there are two samples with "aaa" and two with "bbb" etc. Then you can set …
rep(1:3,each=3) # another true positive &gt;&gt; &gt;&gt; groups &lt;- gl(3,3,labels=letters[1:3]) # organize the data in 3 groups &gt;&gt; &gt;&gt; # basic testing in limma (emprical Bayes) &gt;&gt; require(limma) &gt;&gt; (design1 &lt;- model.matrix
updated 16.2 years ago • Gordon Smyth
Environment for R}, &nbsp;&nbsp;&nbsp; author = {{RStudio Team}}, &nbsp;&nbsp;&nbsp; organization = {RStudio, Inc.}, &nbsp;&nbsp;&nbsp; address = {Boston, MA}, &nbsp;&nbsp;&nbsp; year = {2015}, &nbsp;&nbsp;&nbsp; url = {http://www.rstudio.com
data sets in toto. �So here the &gt; filter condition is (in addition to preliminary filtering by organism &gt; etc., easily done with GEOmetadb) the expression profile.� &gt; &gt; &gt; Now, to get at the expression profile, can I use GEOquery
RNA-seq/Genome/release102/mouse/index_mouse_r102_gffread_salmon_k31", source = "Ensembl", organism = "Mus musculus", release = "102", genome = "GRChm38", fasta = "/home2/ymwang/linqin/RNA-seq/Genome/release102/mouse/transcript_gffread.fa
updated 4.3 years ago • Qin
gt;&gt; &gt;&gt;&gt; Hi Shirley, &gt;&gt;&gt; &gt;&gt;&gt; You can find this information in an organism package. ?org.Hs.eg.db for &gt;&gt;&gt; humans (for example). &gt;&gt;&gt; &gt;&gt;&gt; What will be harder will be getting all the information
<div class="preformatted">Hi. Sorry for the delay I was not in the office for almost a week (and I left the day before this question popped up). Part of the reason for the confusion here is because the ACCNUM field is supposed to represent the source accessions that were used when designing the package. In that sense ACCNUM is kind of an anachronism since I don't think people really desi…
updated 11.3 years ago • Marc Carlson
Chr19" "scaf" &gt; &gt; And then: &gt;&gt; print(BSgenome) &gt; Black cottonwood genome &gt; | &gt; | organism: Populus trichocarpa (Black cottonwood) &gt; | provider: Phytozome (JGI) &gt; | provider version: 3.0 &gt; | release date: January
in 2 (or more) fragments. &gt; &gt; &gt; CEU.RNASeq.geneModel &lt;- easyRNASeq(outputFormat="RNAseq",organism= "HSapiens",count="genes",summarization="geneModels",pattern=".*\\.bam$ ",filesDirectory="../Montgomery2010/bam_hg19/",annotationFile
include tools which facilitate: * annotation (AnnBuilder, annotate). * data management and organization through the use of the S4 class structure (Biobase, marrayClasses, limma). * identification of differentially
then you may already have &gt;&gt;&gt;&gt; everything you need. And if you need another organism, you probably &gt;&gt;&gt;&gt; want to look 1st at making an org package using &gt;&gt;&gt;&gt; makeOrgPackageFromNCBI(). And if...gt;&gt;&gt;&gt; some entirely new database resource (IOW you don't want to make an &gt;&gt;&gt;&a…
gt; &gt; Unfortunately there are no readily available packages for annotating &gt; all the new model organism arrays from Affy. However, the functions to &gt; create your own annotation package do exist. If you look at the &gt; AnnotationForge
GenomeStudio to output summarized beadtype values (no bg or &gt; norm), and GenomeStudio always re-organizes the by Sample_Group. I've learned &gt; to double-check that the order in my targets file is the same as the order &gt; coming
updated 14.5 years ago • Gordon Smyth
my (rather poor) bioinformatics skills. I have been creating TxDb and BSgenome objects for my Model organism to use your package. My final step would be to create a . db file as the one required in your examples&nbsp;org.Hs.eg.db
updated 10.5 years ago • Julie Zhu
not found. &gt;&gt;&gt;&gt; The error was Error in parseKEGGGenome() : Faild to obtain KEGG &gt;&gt; organism &gt;&gt;&gt;&gt; code &gt;&gt;&gt; You need to download the tool set found here &gt;&gt;&gt; (http://www.murdoch-sutherland.com/Rtools
<div class="preformatted">And a belated answer to question 3. To match gene ID to GO categories, goseq calls the getgo function with the genome name provided. It then looks up a local variable called .ORG_PACKAGES and will use the organism package that corresponds to the relevant entry in the list. To access this variable type: &gt; goseq:::.ORG_PACKAGES anoGam...the genome…
Hi, I have analyzed my deep sequencing data with DESeq and successfully generated a heatmap showing differentially expressed miRNAs by using gplots heatmap.2. However, I want to put different colors to the fonts of miRNA names that are shown on y-axis, depending on whether they are up or down regulated. For example, I want to show the names of all down-regulated miRNAs in blue and up-regulated …
H00882 Cocoon syndrome H01746 STING-associated vasculopathy with onset in infancy ORGANISM Homo sapiens (human) [GN:hsa] GENE 23586 DDX58; DExD/H-box helicase 58 [KO:K12646] [EC:3.6.4.13] 64135 IFIH1; interferon induced
updated 6.4 years ago • anamaria
gt; | DBSCHEMAVERSION: 1.0 &gt; &gt; &gt; Athaliana &gt; &gt; Arabidopsis genome &gt; | &gt; | organism: Arabidopsis thaliana (Arabidopsis) &gt; | provider: TAIR &gt; | provider version: 04232008 &gt; | release date: NA &gt; | release
use one of the org.*.eg.db annotation packages for &gt;&gt; &gt; &gt; this (pick up the one for your organism): &gt;&gt; &gt; &gt; &gt;&gt; &gt; &gt; http://bioconductor.org/packages/release/data/annotation/ &gt;&gt; &gt; &gt; &gt;&gt; &gt; &gt; and use the SYMBOL2EG
<div class="preformatted">Looks like the maintainer made changes but forgot to bump the version (svn revision 77544 and 76958; all svn check-ins should be accompanied by version bumps). Should be fixed when 1.9.2 appears. Martin ----- Martin Morgan <mtmorgan at="" fhcrc.org=""> wrote: &gt; On 07/08/2013 09:32 AM, Fr?d?ric Bertrand wrote: &gt; &gt; Hi, &gt; &gt; &…
default for circ_seqs in makeTranscriptDbFromBiomart &gt; &gt;&gt;&gt; to be NULL, instead of any organism (human) specific. &gt; &gt;&gt;&gt; &gt; &gt;&gt;&gt; Regards, &gt; &gt;&gt;&gt; &gt; &gt;&gt;&gt; --Malcolm &gt; &gt;&gt;&gt; &gt; &gt;&gt;&gt; &gt; &gt;&gt;&gt; R…
all of the treatments &gt; (e.g. cancer cells and normal cells from the same subject; different &gt; organs from the same mouse). In this case, the "error" for testing &gt; treatment effects is biological sample * treatment, and the
change the default for circ_seqs in makeTranscriptDbFromBiomart to be NULL, instead of any organism (human) specific. Regards, --Malcolm R version 2.14.0 (2011-10-31) Platform: x86_64-apple-darwin9.8.0/x86_64 (64-bit) locale
Chr16" "Chr17" "Chr18" [19] "Chr19" "scaf" And then: print(BSgenome) Black cottonwood genome | | organism: Populus trichocarpa (Black cottonwood) | provider: Phytozome (JGI) | provider version: 3.0 | release date: January 2010
change the default for circ_seqs in makeTranscriptDbFromBiomart &gt; to be NULL, instead of any organism (human) specific. &gt; &gt; Regards, &gt; &gt; --Malcolm &gt; &gt; &gt; R version 2.14.0 (2011-10-31) &gt; Platform: x86_64-apple-darwin9.8.0
<div class="preformatted">Dear Benilton, thanks for your e-mail. I'm sorry for not having writed back till now, but I have just read it (I don't know why it was not labelled, so I lost it among all the others from bioconductor....) I will try to analyze the arrays I have pending with your script. I will write back soon! Thank you again! Best regards, Elena 2013-11-18 18:44 GMT+01:00 Ben…
<div class="preformatted">Hi all, Benilton, could you please update us if there is being some progress in getting the annotation files for HTA 2.0 affymetrix arrays? I am following this topic but I think there's not been any more comment after yours on 11/18/13 and I wonder whether I've missed something about the topic. Thank you in advance! Best regards, Elena Bioinformatician Scientif…
<div class="preformatted">Dear Herve, Sean, and All After updating my R, now I can use the liftOver() in rtracklayer package. However I met a problem for SNP rs171. It is on chr 1 in build37.3, but on chr7 in build 36.3. Please check the following link: http://www.ncbi.nlm.nih.gov/projects/SNP/snp_ref.cgi?rs=171 In this case, does liftOver work? How many SNPs in NCBI dbSNP like this, map…
nturaga1 at="" jhmi.edu="">",biocViews = &gt;&gt;&gt;"DNAMethylation",genomebuild = "NCBI Build 36",organism = &gt;&gt;&gt;"Human",species &gt;&gt;&gt;= "Homo Sapiens") &gt;&gt;&gt; makePdInfoPackage(pkg,destDir=".") &gt;&gt; &gt;&gt;==================================================================== ===== &gt;&gt;== &…
Chr16" "Chr17" "Chr18" [19] "Chr19" "scaf" And then: print(BSgenome) Black cottonwood genome | | organism: Populus trichocarpa (Black cottonwood) | provider: Phytozome (JGI) | provider version: 3.0 | release date: January 2010
source\_url: http://hgdownload.cse.ucsc.edu/goldenPath/dm6/bigZips/ organism\_biocview: Drosophila\_melanogaster nmask\_per\_seq: 3 SrcDataFiles: AGAPS masks: dm6.agp.gz from http://hgdownload.cse.ucsc.edu
updated 9.1 years ago • nadia.goue
these basics steps are &gt; explained? which steps are you refrerring to? by the way: which array/organism are you using. and are you doing one or dual color experiments? best T. &gt; Thank you in advance &gt; Massimo &gt; &gt; &gt; &gt; &gt
updated 16.2 years ago • Tobias Straub
<div class="preformatted">Hi marc, Thanks for the tip, i realized that my function was too slow. I agree with you. Getting all GO in one shot is a much better approach. On 03/31/2011 09:23 PM, Marc Carlson wrote: &gt; Hi David, &gt; &gt; If this was your function you would 1st of all want to just pass in a &gt; big vector (with your universe of transcript IDs in it) to get …
cottonwood) genome as provided by Phytozome (v3, 2013) stored in Bioconductor &gt; Version: 3.0 &gt; organism: Populus trichocarpa &gt; species: Black cottonwood &gt; provider: Phytozome (JGI) &gt; provider_version: 3.0 &gt; release_date
<div class="preformatted">Can you please give us the results of with(ndf, table(MISMATCH, PROBE_CLASS)) the one thing that pdInfoBuilder expects is the PROBE_CLASS field to have the word 'experimental' for thé probes that are not controls. b On 26 Aug 2013 16:44, "Nitesh Turaga" <nturaga1@jhmi.edu> wrote: &gt; Hi Dr.Carvalho, &gt; &gt; Please let me know your thought p…
<div class="preformatted">Dear BioC Users, Does anyone have a reference for (or a good definition of) median- interquartile normalization? Is it the same as interquartile normalization? (If not, I would like a reference/definition of both) I have looked for such a definition in the literature, but I haven't found a satisfactory one. Thank you, Monnie McGee Monnie McGee, Ph.D. Associate …
metabolism in diverse environments" &gt;&gt; [5] "ko00710 Carbon fixation in photosynthetic organisms" &gt;&gt; [6] "ko00562 Inositol phosphate metabolism" &gt;&gt; &gt;&gt; seems to be about what you want, or &gt;&gt; &gt;&gt; &gt;&gt; head(xpathSApply
updated 13.8 years ago • Voke AO
<div class="preformatted">Bioconductors: We are pleased to announce Bioconductor 2.11, consisting of 610 software packages and more than 650 up-to-date annotation packages. There are 58 new software packages, and many updates and improvements to existing packages; Bioconductor 2.11 is compatible with R 2.15.1, and is supported on Linux, 32- and 64-bit Windows, and Mac OS. This release inc…
lt;- new("NgsExpressionPDInfoPkgSeed", ndfFile = ndf, xysFile = xys, &gt;&gt;&gt;&gt; author = "FJ", organism = "Apple", species = "Malus x Domestica cv.GD") &gt;&gt;&gt;&gt; &gt;&gt;&gt;&gt; makePdInfoPackage(arrays, destDir = getwd()) &gt;&gt;&gt;&gt; &gt
annotate Imports: methods, AnnotationDbi License: Artistic-2.0 organism: Homo sapiens species: Human manufacturer: Affymetrix chipName: hgu133a2 manufacturerUrl: http://www.affymetrix.com
as provided &gt;&gt; by Phytozome (v3, 2013) stored in Bioconductor &gt;&gt; Version: 3.0 &gt;&gt; organism: Populus trichocarpa &gt;&gt; species: Black cottonwood &gt;&gt; provider: Phytozome (JGI) &gt;&gt; provider_version: 3.0 &gt
Here is the previous query with a more descriptive subject. -----Original Message----- From: McGee, Monnie Sent: Thu 10/23/2008 11:14 AM To: bioconductor at stat.math.ethz.ch Subject: RE: Bioconductor Digest, Vol 68, Issue 23 Dear List, Is there an elegant way to obtain the name of a probe set from an Affymetrix platform (doesn't matter which one) corresponding to a given ENTREZ gene ID? It s…
<div class="preformatted">Bioconductors: We are pleased to announce Bioconductor 2.12, consisting of 671 software packages and more than 675 up-to-date annotation packages. There are 65 new software packages, and many updates and improvements to existing packages; Bioconductor 2.12 is compatible with R 3.0, and is supported on Linux, 32- and 64-bit Windows, and Mac OS X. This release incl…
1:17) is likely not to work with S.pombe. You can see what the &gt; chromosome names are in your organism by inspecting the probeAnno object. &gt; &gt; Best wishes &gt; Wolfgang &gt; &gt; On Sep/8/10 10:33 PM, sohkhan at notes.cc.sunysb.edu
Sent from my Droid Charge on Verizon 4GLTE "bioconductor- request@r-project.org" wrote: Send Bioconductor mailing list submissions to bioconductor@r-project.org To subscribe or unsubscribe via the World Wide Web, visit https://stat.ethz.ch/mailman/listinfo/bioconductor or, via email, send a message with subject or body 'help' to bioconductor-request@r-project.org You c…
API changes - Support for new schemaless chip packages to allow more flexible suport of non-model organisms in chip packages. - Support for Inparanoid8 objects which contain data from the most recent release of inparanoid
I am running Combat on the attached files. 2 channel array (with reference). Problem is the adjusted file returns an added column of numbers where CLID should be. This column then stops delivering said numbers around line 3154, returning to CLID, shifting all the information and data to the left. I am stumped as to why this is happening. Please advise. thanks, tam Reading Sample Information…
Bioconductors: We are pleased to announce Bioconductor 2.13, consisting of 749 software packages, 179 experiment data packages, and more than 690 up-to-date annotation packages. There are 84 new software packages, and many updates and improvements to existing packages; Bioconductor 2.13 is compatible with R 3.0.2, and is supported on Linux, 32- and 64-bit Windows, and Mac OS X. This release in…
F,prefix="primeview",fileName="primevie wHumanGeneExprs.txt",metaDataSrc=c("DBSCHEMA"="HUMANCHIP_DB","ORGANISM "="Homo sapiens","SPECIES"="Human","MANUFACTURER"="Affymetrix","CHIPNAME"="Pri meView Human Gene Expression Array","MANUFACTURERURL
updated 12.8 years ago • wang peter
1,253 results • Page 21 of 21
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