193 results • Page 2 of 4
database documentation, the bioconductor mailing list, the > BSgenome documentation, and the goseq documentation, I am still very > confused about whether I can use the assembly 4 package that Herv? > posted in goseq...Just to clarify, goseq is not my package so I can't "post" anything in it, whatever that means. I assume you are talking about the BSgenome.Amellifera.BeeBase.…
I’m currently attempting to perform an analysis using GOseq on the up regulated genes of a RNAseq experiment. The thing is I keep getting a plot as the one I attached
updated 8.6 years ago • dlsoltero
Hi all,   I am trying to install goseq as specified [here. ](https://bioconductor.org/packages/release/bioc/html/goseq.html) This is the commands I put in: R source...https://bioconductor.org/biocLite.R") biocLite("goseq") At the end of the installation, it prints this: The downloaded source packages are in       &n…
updated 6.4 years ago • philipp.voss
I have followed this [tutorial](https://f1000research.com/articles/5-1438/v2) for edgeR. On this [side](https://toolshed.g2.bx.psu.edu/repository/display_tool?repository_id=f599adf23b671cad&tool_config=%2Fsrv%2Ftoolshed%2Fmain%2Fvar%2Fdata%2Frepos%2F002%2Frepo_2703%2Fgoseq.xml&changeset_revision=ade933eff007) it appears I could run `` goseq `` when I have created the following fil…
updated 6.6 years ago • mictadlo
Hello all, I am encountering problems with the goseq package. I did some analysis few months ago without any problems and I now need to reuse the script for another part of...inequality constraints</pre> Because I updated my Bioconductor packages recently (I think I used goseq\_1.16.2 before) and I am using an old R version (still the one for Snow Leopard), I am thinking that it could be …
updated 8.9 years ago • Merienne Nicolas
for you to use a genome which is not supported (if it's not in UCSC then it's not supported in goseq) then you are right in that you will need the annotation (gene length) and the mapping from geneids to GO terms. It's not enough...just to have the genome in order to use goseq. Cheers, Alicia On 25/02/12 6:32 PM, "bioconductor-request at r-project.org" <bioconductor-request at="" r-project.…
I have successfully conducted a gene ontology analysis using goseq. In presenting the findings of the analysis (i.e., the standard output generated by the \`goseq\` function) to a colleague, he...function were those associated with any given significant GO or KEGG term arising as output of the \`goseq\` function. The columns \`numDEInCat\` and \`numInCat\` clearly summarize this information (i.e…
updated 6.5 years ago • JMallory
Hello, I've tried to install the package goseq with: if (!requireNamespace("BiocManager", quietly = TRUE)) install.packages("BiocManager") BiocManager::install("goseq") But...R/library/geneLenDataBase’ ERROR: dependency ‘geneLenDataBase’ is not available for package ‘goseq’ * removing ‘/usr/local/lib64/R/library/goseq’ The downloaded source packa…
updated 4.6 years ago • Raito92
img alt="" src="http://i.imgur.com/K8MzXPo.png" style="height:504px; width:504px"/> Hi, I use goseq and with the Wallenius approximation I get 264 BH adjusted significant overrepresented categories, with the sampling
updated 8.9 years ago • idomtamir
Hi, I've been following the vignette, but I keep getting the following error with supportedOrganisms() from goseq: __Error in matrix(unlist(pairs), nrow = 2) : &nbsp; 'data' must be of a vector type, was 'NULL'__ Is there something I am doing wrong? Many thanks in advance!! Victoria R version 3.3.2 (2016-10-31) -- "Sincere Pumpkin Patch" Copyright (C) 2016 The R Foundation for…
updated 7.1 years ago • starbug16
I'm getting a warning message when I try to run Gene Ontology analysis with *goseq* using human genome assembly GRCh38 (hg38). I know that hg38 isn't natively supported by *goseq*, but *goseq* will fetch *goseq...installed. Thus, I run the following code: ``` library(TxDb.Hsapiens.UCSC.hg38.knownGene) library(goseq) # load toy dataset aa = c(1,1,1,1,1,1,1,1,1,1,1,0,1,1,1,1,1,1,1,1) names(aa) …
updated 3.2 years ago • Nikolay Ivanov
Hi, I have a microarray data that I would like to do GO analysis using GOSeq. However, I have ENTREZ gene ids. When I am trying to convert ENTREZ ids to ENSEMBL ids, I lose several of my genes from the
updated 8.0 years ago • Mehmet Ilyas Cosacak
s fine. While well represented in the literature, I'm wondering if this approach is not redundant? GOseq is supposed to prevent biases introduced by the greater power to detect DE in longer transcripts. However, since the...have effectively compensated for any gene length effects, it seems like the subsequent use of GOseq could result in more false <s>positives&nbsp;</s>&nbsp…
which are ensembl Ids I wanted do GO analysis for this list of genes. How can I do this from the GOseq I went through vignette which is running the GOseq from the DE genes output, my genes list are not from the DE this are obtained
updated 3.1 years ago • Lucky
nbsp; Anyone has some advice on how to get it running?&nbsp; Thank you, &nbsp; &gt; library(goseq) Indlæser krævet pakke: BiasedUrn Indlæser krævet pakke: geneLenDataBase Error: package or namespace load failed...goseq’ in loadNamespace(j &lt;- i\[\[1L\]\], c(lib.loc, .libPaths()), versionCheck = vI\[\[j\]\]): &nbsp;der er ingen pakke med navn ‘GO.db’ &gt; so…
updated 6.6 years ago • veerle
writing because of some warnings that appeared when running the&nbsp;_nullp_&nbsp;command. It seems GOseq cannot find the gene lenghts for my data ('hg38','ensGene') in genLenDataBase. I installed the TxDb.Hsapiens.UCSC.hg38.knownGene
updated 7.6 years ago • webquelzinhablue
Following the instructions on https://bioconductor.org/packages/devel/bioc/vignettes/goseq/inst/doc/goseq.pdf To see what genomes are in the local database, I am told to type: __supportedOrganisms()__ ...which returns...GenomeInfoDb\_1.6.3__ __\[10\] IRanges\_2.4.8 S4Vectors\_0.8.11 BiocGenerics\_0.16.1__ __\[13\] goseq\_1.22.0 RSQLite\_1.1-2 geneLenDataBase\_1.6.0__ __\[16\] BiasedUrn\_1.0…
<div class="preformatted"> Hi all and M. Carlson I am now working on an archaea, which is not a common organism. I want to use goseq to do the GO analysis of my RNAseq data.In order to creat the category mappings(relationship between GO and gene id), I...Hi all and M. Carlson I am now working on an archaea, which is not a common organism. I want to use goseq to do the GO analysis of my RN…
Hello Sir, I am using it for non-model organisms. 1) I have a set of differentially expressed genes, plus the go term related to genes. 2 ) The command in R in need to use is: goseq(pwf, genome, id, gene2cat = Null) I understand that for gene2cat argument I need to mention my list of genes with their go term.Correct...expressed genes, plus the go term related to genes. 2 ) The command in…
updated 3.9 years ago • kumararya563
differentially expressed genes checked for over-reppresentation using the procedure available in the goseq package. The topGO package (see, for example, the chapter 7.4 of the included vignette) allows this kind of visualization...data. Any idea how this kind of visualization can be produced for RNAseq data inspected using goseq? Any idea would be appreciated! Regards, Paolo [[alternat…
div class="preformatted">Dear Matthew, I am getting the following error when using goseq. Any idea what may cause it? Thanks, Adi &gt; pwf=nullp(genes,bias.data=cntbias) &gt; gocats=as.list(org.Hs.egGO2ALLEGS) &gt...GOr=goseq(pwf,gene2cat=gocats) Using manually entered categories. Calculating the p-values... Error in dWNCHypergeo(num_de_incat
updated 11.1 years ago • Tarca, Adi
on the following error. It's generated when I attempt to access the supported organism list in goseq.&nbsp; __&gt; supportedOrganisms()__ __Error in getNodeSet(doc, "//table\[@class='descTbl'\]")\[\[1L\]\] :&nbsp; &nbsp; subscript out of bounds__
updated 7.1 years ago • jesykamelendez
Hi All, I am using GOseq as part of the Trinity pipeline to perform gene ontology testing for genes in a&nbsp;_de novo_&nbsp;transcriptome assembly...Hi All, I am using GOseq as part of the Trinity pipeline to perform gene ontology testing for genes in a&nbsp;_de novo_&nbsp;transcriptome assembly. I used edgeR to perform DGE analysis comparing groups that were treated with a che…
updated 5.8 years ago • mart1139
Hello everyone, I am new to this forum so I'm apologizing in advance if I am not posting in the most formal way. I am using the goseq package from bioconductor in order to perform enrichment for markers that are differentially methylated (limma output). These markers have been measured&nbsp; according to CpG arrays from 450K illumina (i.e.&nbsp;cg07790169) and I am retrieving them on uc…
updated 6.1 years ago • dusan.petrovic
r-project.org Subject: Re: [BioC] Visualising the GO structure (RNA-seq) using topGO and goseq Message- ID: &lt;4D9270E1.1000303@fhcrc.org&gt; Content-Type: text/plain Hi Paolo, Not quite sure what you want from your...expressed genes checked for &gt; &gt; over-reppresentation using the procedure available in the goseq package. The &gt; &gt; topGO package (see, for examp…
Recently I started using it for pathway analysis. It works well for human mRNAseq DGE data. But I encountered some problem with non-model samples. I hope I could get some help from you. The specific problem I have is with cat genome. I looked up the supported genome: &gt; supportedGenomes()[,1:4] <code>12 felCat5 Cat Sep. 2011 ICGSC Felis…
updated 8.7 years ago • xyliu00
The vignette of GOseq details in section 6.8 how to correct for total&nbsp;read&nbsp;count bias (per gene). The code used to calculate total read
updated 7.0 years ago • Christopher Conley
I did the GO terms enrichment analysis using GOSeq, after that I want to access the esIDs in the significantly enriched terms. I tried to extract esIDs using `` org.Hs.eg.db...in `` GO.wall `` report is 124, so is there any method to directly access the genes in GO terms in GOSeq
updated 5.4 years ago • mico
Hello there, I have a question concerning usage of GOseq for testing custom gene list (approx. 1k genes) enrichment. I am not sure about the `use_genes_without_cat` argument value
updated 5.2 years ago • kubovcij
of mac. Thanks in advance, Steve &gt; source("http://bioconductor.org/biocLite.R") &gt; biocLite("goseq") BioC_mirror: http://bioconductor.org Using R version 2.15, BiocInstaller version 1.4.7. Warning: unable to access index...http://brainarray.mbni.med.umich.edu/bioc/bin/macosx/leopard/contrib/2 .15 Installing package(s) 'goseq' Warning: unable to access index for repository http://li…
updated 11.8 years ago • steve Shen
I am suddenly having trouble using goseq for supportedOrganisms as bioconductor suddenly seems unable to retrieve the appropriate data from the UCSC database
updated 6 weeks ago • thomas
Hi! Does the goseq package always use the most current release of an Ensembl genome or is it possible it may be using previous archives
updated 8.1 years ago • mrodrigues.fernanda
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...package that corresponds to the relevant entry in the list. To access this variable type: &gt; goseq:::.ORG_PACKAGES anoGam Arabidopsis bosT…
Hi Guys Here I am again with another question about goseq. I am following the goseq tutorial. I am manually inserting my length and go data, since the combination o fmy species genome...and gene ID is not supported by goseq.&nbsp; I ran the following code, and it ran fine as you can see in my output: <code>GO.wall &lt;- goseq(pwf, gene2cat = Biomart.GOdata...categories in the ca…
updated 8.0 years ago • mrodrigues.fernanda
Hi, I am thinking about switching from GoStats to GoSeq. Is there a built in possibility to use the ENSEMBL transcript annotation or can I only use ENSEMBL genes? Do I have to...Hi, I am thinking about switching from GoStats to GoSeq. Is there a built in possibility to use the ENSEMBL transcript annotation or can I only use ENSEMBL genes? Do I have to annotate
updated 8.9 years ago • idomtamir
over representation) analysis of GWAS/QTL data distributed over a genome, is it possible with goseq?&nbsp; I could not find any useful tutorials/manual -- could someone kindly show (1) required inputs (format, etc.; e.g. we have...coordinate locations", "a small segments of a genome region to test"), (2) command line to run R/goseq (so that we can build a pipeline to run as routine), and (3) …
updated 5.7 years ago • zhu
I am trying to run goseq package in R, working with human data with hg19. I followed the vignette instructions to create "gene.vector", but I am...I am trying to run goseq package in R, working with human data with hg19. I followed the vignette instructions to create "gene.vector", but I am getting
updated 6.6 years ago • pereyra.s
Has anyone else encountered any issues with using mm10 in the goseq package: <pre> &gt; pwf &lt;- nullp(genes, "mm10", "geneSymbol") Can't find mm10/geneSymbol length data in genLenDataBase... Found the
updated 8.2 years ago • Bohdan Khomtchouk
Recently, I have tried to apply GOSeq to RNA-seq expressions after voom adjustment. It has just ocurred that differential expression and gene length were
updated 6.2 years ago • joelrosa
Hi all,&nbsp; I am using goseq to correct for RNA-seq length bias. Since my dog genome (canFam3) is not supported in goseq database, I tried to make TXDb...nbsp;&nbsp; __If it's correct, it could potentially be a tutorial and benefit other users since the goseq documentation isn't very self-explanatory. &nbsp;__ I have posted a question in BioStars but I think I could potentially..…
updated 8.0 years ago • CandiceChuDVM
nbsp; Dear all, I am running GOseq on a custom annotated dataset. I am getting a nicely looking output: list of enriched and depleted GOterms for my different
updated 5.7 years ago • TB18
Relevant sessionInfo(): R version 3.2.2; BiocInstaller\_1.18.4 ; goseq\_1.20.0 I am relatively new to R and to Bioconductor packages. I am using goseq for GO enrichment analysis of mouse RNA...GO term enrichment analysis despite their NA pwf values? (5) I'm assuming that at this stage in the goseq pipeline the NAs have nothing to do with whether the genes have GO annotations, correct? (I cannot …
updated 8.6 years ago • mjnolte
resolve&nbsp;__length bias__)__: &nbsp;__ Since the dog genome assembly canFam3 is not supported in goseq&nbsp;database, I have to make my own \`bias.data\` to perform \`nullp\` in goseq. I was able to perform \`GO.wall=goseq(pwf,gene2cat...bias into consideration. However, "limiting GO categories and other category based tests" as \`GO.MF=goseq(pwf,gene2cat=geneID2GO, test.cats=c("G…
updated 7.9 years ago • CandiceChuDVM
Hi, I've performed KEGG pathway analyses using the GOseq package and now I was wondering how do I know which genes were included in the "numDEInCat"? See below for example:&nbsp...Hi, I've performed KEGG pathway analyses using the GOseq package and now I was wondering how do I know which genes were included in the "numDEInCat"? See below for example:&nbsp; <table...find anything reg…
updated 7.3 years ago • Xavier
Hi! I am using goseq on some bovine data and I am using Ensembl IDs for bovine genome UMD3.1, which is not supported by goseq, so I had to input
updated 8.0 years ago • mrodrigues.fernanda
Hi, I've performed gene ontology analysis with GOseq using the standard ontologies, as well as using KEGG and Reactome. When using the default ontologies or KEGG, the function
updated 4.0 years ago • hasse.bossenbroek
pathway analysis. I have used the gage package and I was looking online about another package called goseq that takes into account length bias. However, when I run the code I get an error. How to solve that as I am not sure what the...error means? ```r library(goseq) supportedOrganisms() %&gt;% filter(str_detect(Genome, "hg")) #Step 1 #prepare the results for goseq de.genes&am…
updated 2.1 years ago • m.glymenaki
was also performed through the analyze_diff_expr.pl script. The function calls the R package **goseq**, and [as stated here][2], the output looks this way: *Two outputs will be generated for each set of genes tested for functional...Trinity-Differential-Expression [2]: https://github.com/trinityrnaseq/trinityrnaseq/wiki/Running-GOSeq [3]: https://i.ibb.co/WDvmhxb/41390-2018-192-Fig3-HTML…
updated 4.6 years ago • Raito92
div class="preformatted">Hi, I have got an error while i have been running goseq R package using UCSC known gene ID such numbers, 1,2,...27315.(27181 genes). When i computed pwf. it was fine. but, In getgo function
updated 14.0 years ago • sunghee OH
div class="preformatted">Hello, I've been trying to install goseq on R-2.15.2 but one of the dependencies, RCurl is not installing. I've compiled curl and curl-config (7.28.0); there is also
updated 11.5 years ago • Dave Tang
Hi, I'm running pathway analysis with goseq but had the error :&nbsp;In pcls(G) : initial point very close to some inequality constraints : when plotting the nullp. I'm...Hi, I'm running pathway analysis with goseq but had the error :&nbsp;In pcls(G) : initial point very close to some inequality constraints : when plotting the nullp. I'm not
updated 6.7 years ago • heikki.sarin
Hello I got this error when using supportedGenomes() in goseq package: <pre> &gt; library(goseq) Loading required package: BiasedUrn Loading required package: geneLenDataBase &gt; head
updated 6.5 years ago • mgdrnl
div class="preformatted"> Hello, I performed an analysis with EdgeR followed by an analysis with GoSeq and then I got this error message, saying there is an error in if (matched_frac == 0) { :missing value where TRUE/FALSE is required
updated 11.4 years ago • Guest User
there are now two copies of curl and curl-config (the old and new version). I will just do the goseq analysis on my own Ubuntu box. Thanks again for your help, Dave </dtenenba></davetingpongtang></dtenenba></mtmorgan></div
updated 11.5 years ago • Dave Tang
Hi! I am trying to use the package goseq, but when I try running the function supportedOrganisms() R says it cannot find it. Does anyone know what might be the reason...grDevices utils \[7\] datasets methods base other attached packages: \[1\] KEGG.db\_3.2.2 goseq\_1.22.0 \[3\] geneLenDataBase\_1.6.0 BiasedUrn\_1.07 \[5\] GOstats\_2.36.0 graph\_1.48.0 \[7\] Category\_2.36.0 GO.db\_3.…
updated 8.1 years ago • mrodrigues.fernanda
sum(exonBaseMean), sig = max(sig) ) %&gt;% ungroup() I can then run goseq using&nbsp; the lengths as the bias data: genes &lt;- retained_genes$sig names(genes) &lt;- retained_genes$gene_id bias.data...CY9MhRQ.png) And then proceed to test for category enrichment: go.retainted.length &lt;- goseq(pwf, genome='hg19',…
updated 6.7 years ago • i.sudbery
biocLite.R")Bioconductor version 2.11 (BiocInstaller 1.8.3), ?biocLite for help&gt; biocLite("goseq")'BiocInstaller' package not in repository http://bioconductor.org/packages/2.11/bioc, using 'http://bioconductor.org
updated 11.4 years ago • Abhishek Pratap
&nbsp; Hi all, There have been a number of questions asked on this topic (I've linked the relevant threads below), but I'm not sure if anyone has found a working solution. &nbsp;I have run GOSeq on my gene set and am looking to __identify the genes in each category (numDEInCat)__. &nbsp;Here is what I've done so far. &nbsp...relevant threads below), but I'm not sure if anyone ha…
I've found myself in the situation where goseq fails with some relatively extreme numbers (derived from ChIP-Seq data with extreme changes in the IP target) and have
updated 24 months ago • Steve Pederson
<div class="preformatted">Hi, all I am trying to use goseq for RNAseq data analysis of a non-native bacteria, I fetch the genelength data and GO term data by using ensembl Perl API. Differential expression was done by DESeq2. After data run pwf of goseq, error occurred as following: ### Error in if (hi &lt;= low) { : missing value where TRUE/FALSE needed Have any one met this befor…
193 results • Page 2 of 4
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