1,253 results • Page 7 of 21
Warning message: no not accessible  I was wondering whether there is a specifically way to organize the bam file which could be read in the dba project.  Thank you so much.       &nbsp
updated 10.7 years ago • yijing.su
Hi All, Could anyone please elucidate advantages of having an Annotation package for an organism or point me to any documentation that clearly lists all the various thoughts behind coming up with an Annotation
updated 12.6 years ago • Rameswara Sashi Kiran Challa
i did not find genesets my organism of interest in the search page of GSEA: http://www.gsea-msigdb.org/gsea/msigdb/search.jsp Can I use the pathawy genesets
updated 4.7 years ago • MOHAMMAD
Hi there. I am trying to find a way to get a specific list of the additional parameters that are specified within the `...` argument of a function inside a library. How do you do that? In particular I would like to know the parameters accepted by the function `viewPathway` inside the ReactomePA package. By typing `formals(viewPathway)` I get: $pathName $organism [1] …
updated 5.8 years ago • lucap
sequence.gff3") ``` which yields the error message: ``` Error in .checkExtractVersions(gff, organism, genomeVersion, version) : The file name does not match the expected naming scheme of Ensembl files ( <organism>.<genome...version="">.<ensembl version="">) hence I cannot extract any information from it! Parameters 'organism', 'genomeVersion' and 'version' are thus required!…
updated 4.7 years ago • Torkel
id format ids&lt;-bitr(names(original_gene_list), fromType = "ENSEMBL", toType = "ENTREZID", OrgDb=organism) dedup_ids = ids[!duplicated(ids[c("ENSEMBL")]),] df2 = g[g$gene_id %in% dedup_ids$ENSEMBL,] df2$Y = dedup_ids$ENTREZID # Create a vector...decreasing = TRUE) ``` ```{r} kegg_organism = "mmu" kk2 &lt;- gseKEGG(geneList = kegg_gene_list, organism = kegg_organi…
updated 4.2 years ago • ICELANDICWATER
<div class="preformatted">Dear all, I have noticed that BSgenome.Mmusculus.UCSC.mm10 does not contain entries for upstream sequences (upstream1000, upstream2000, upstream5000) like for example BSgenome.Mmusculus.UCSC.mm9 does (see bellow). Is there a reason for this? Thank you, Diego &gt; library(BSgenome.Mmusculus.UCSC.mm9) &gt; Mmusculus Mouse genome | | organism: Mus musculus …
c. homology package now maps internal HomoloGeneIds to homoData objects that has slots for organism name, LocusLink ids, internal HomoloGeneIds, GenBack Accession numbers, type of similarities, percent of identity...and urls for homologous genes in other organism. Environment LL2HGID maps LocusLink ids to internal HomoloGeneIds. d. New annotation data…
etc. at the conference website: http://www.camda.info We look forward to a lively contest! The organizers and chairs of CAMDA 2013 Chairs: Joaquin Dopazo, CIPF, Spain Sepp Hochreiter, Johannes Kepler University, Austria...David Kreil, Boku University, Austria Simon Lin, Marshfield Clinic, U.S.A. Local organizer: Djork-Arné Clevert, Johannes Kepler University, Austria Contact: camda@bioinf.jk…
<div class="preformatted">hi all, I try to use ABPkgBuilder (session info below) with following code (partly from the vignette) ##### library(AnnBuilder) read.table(file.path(.path.package("AnnBuilder"), "data", "thgu95a"), sep = "\t", header = FALSE, as.is = TRUE) myBase &lt;- file.path(.path.package("AnnBuilder"), "data", "thgu95a") myBaseType &lt;- "gb" myDir &lt;…
wrong? My script at least: library(KEGGgraph) tmp &lt;- tempfile() retrieveKGML("00900", organism="csav", destfile=tmp, method="auto", quiet=TRUE) mapkKGML &lt;- system.file("extdata", "csav00900.xml", package = "KEGGgraph") mapkG
updated 20 months ago • fernanda.backsouza
Suppose on NCBI BLAST website I insert one query sequence and hit BLAST with Homo sapiens as organisms. I extract the description of the first hit and paste it aside the sequence in the excel sheet (same round different
updated 3.7 years ago • Prateek
www.ensembl.org"), 10) ###marts providing annotation for specific classes of organisms### head(biomaRt::listDatasets(biomaRt::useMart("ENSEMBL_MART_ENSEMBL", host = "www.ensembl.org")), 100
updated 4.1 years ago • adeler001
I now have an expression profile of an organ at various developmental time periods, such as 3 replicates in the first week, 5 replicates in the second week, 4 replicates
updated 2.8 years ago • guang-hui
Warning message: In file(con, "r") : cannot open URL 'http://www.UniProt.org/UniProt/?query=organism:9606&amp;format=tab&amp;columns=id': HTTP status was '301 Moved Permanently'.</pre> Even after setting internet to true
updated 10.0 years ago • beingseema03
preformatted">Can anyone direct me to an example of using hyperGTest with a KEGGHyperGParams? My organism is yeast and -- since my experimental data is from proteomics -- I have been happy using the YEAST annotation package
div class="preformatted">HI all, I have paired-end RNAdata from five different tissues of the same organism, I calculated the read counts using HTSeq tools and now I want to see which are the transcripts which are differentially
updated 13.3 years ago • Srikanth Manda Srinivas
the entrez ID and the logfoldchange in it. Error in spia(de = DE\_Colorectal, all = ALL\_Colorectal, organism = "hsa",&nbsp; : &nbsp; de must be a vector of log2 fold changes. The names of de should be included in the refference array! &nbsp
updated 9.5 years ago • saamar.rajput
ENSG00000174871","ENSG00000112531") GOsim\_matrix &lt;- mgeneSim(genes=mytestgenes,ont="MF",organism="human",measure="Wang",verbose=T) I am assuming that GOsemsim only works with enrez ids and I was wondering if there is
updated 9.3 years ago • saadmurtazakhan
researchers who use Bioconductor packages regularly. Pseudomonas aeruginosa is not one of the 20 organisms currently incorporated in OrgDb, but it looks as though many tools exist to construct a properly formatted database
updated 4.7 years ago • Thomas.H.Hampton
Can anyone explain the "CalcNormFactors" normalization process in edge r?&nbsp; I have RNAseq data from insect antennae. I do not have a genome assembly for my organism, but I did assemble the transcriptome using trinity. I then retrieved my transcripts of interest (chemosensory genes...in edge r?&nbsp; I have RNAseq data from insect antennae. I do not have a genome assembly for my organi…
updated 7.0 years ago • phickner2
I am new regarding the KEGG pathway enrichment analysis. I have an in-house assembled genome and used it for RNAseq analysis. I did KEGG annotation using GhostKOALA and then used the KO annotation for GSEA analysis using ClusterProfiler (version 4.4.4). It ran smoothly but the enrichment result was a list of KO entries. I guess it makes sense since I used this KO annotation as the TERM2GENE input…
updated 3.1 years ago • Susanne
Hello, I have been pointed out [here](https://support.bioconductor.org/p/100092/#100095) that is possible to use [limma](https://support.bioconductor.org/p/76482/) to do any analysis, including KEGG or GO analyses of a new species. How is it possible to create an annotation database using annotationHub() or by supplying the gene.pathway data.frame directly for my non-model species? Thank you i…
updated 8.3 years ago • mictadlo
Hi, I'm running a WGCNA analysis to detect correlating genes between a Virus and a host. My issue here is, that, over the course of the infection, the relative amount of host transcripts is decreasing from 100% to around 20%, so by normalizing over host and virus transcripts together, all finer differential dynamics are overshadowed by this trend. For a DE-analysis with DESeq2, I run the whole a…
updated 4.9 years ago • wrzl
Loading required package: RCurl Loading required package: bitops discarding data from other organisms Populating gene2pubmed table: table gene2pubmed filled Getting data for gene2accession.gz discarding data...data from other organisms Populating gene2refseq table: table gene2refseq filled Getting data for gene2unigene discarding data from...other organisms Populating gene2unigene table: table ge…
Dear Marc and Hervé, I believe the AnnotationForge package is currently not working correctly. Perhaps due to an update in SQL functions? To keep it as simple as possible, I simply tried to reproduce the worked example in Marc's "Making Organism packages" vignette. It required one small modification on the last line to run (type="source"), so I'll paste in the whole code here: ``` library(…
two conditions (control and mutant) using S.pombe as a spike-in (because the antibody works in both organisms). The reason because we add spike-in is that the antibody is not very efficient so we wanted to normalise the immunoprecipitation
updated 4.4 years ago • maria.soler
for rice (oriza sativa - osa). There is KEGG's pathway data for rice, but rice is not among those organism in the extData directory of the SPIA package. Does anyone has created their own pathway data to give it as input to
updated 15.1 years ago • Lourdes Peña Castillo
there will be a Bioconductor Developers' Meeting on 4.+5. April 2007 in Lausanne, Switzerland. Local organizer is Darlene Goldstein and the Vital IT centre. Mark your calendars. Details of the programme will be announced soon
updated 19.0 years ago • Wolfgang Huber
<div class="preformatted">I have a use case that I am not sure the best way to proceed. I have a non-model organism for which we would like to know the sequence for a set of genes. It's a bird species, and I can for example align to the zebra...preformatted">I have a use case that I am not sure the best way to proceed. I have a non-model organism for which we would like to know the seq…
updated 11.3 years ago • James W. MacDonald
When I used the demo sqlite file, there are some outputs ```r &gt;sqlfile_demo &lt;- getSQLiteFile(destdir = "~/bin/Rpack", destfile = "GEOmetadb.sqlite_demo.gz",type="demo") &gt;con &lt;- dbConnect(SQLite(),sqlfile_demo) &gt;getBiocPlatformMap(con)[1:5,] title gpl bioc_package…
updated 2.2 years ago • Lee
<div class="preformatted">As low as 0.5 for pearson and 0.8 for spearman But I'm not holding up my data as a shining example Surely if there is a lot of natural variation in the biological system, then you're going to get large variation between biological replicates. -----Original Message----- From: Naomi Altman [mailto:naomi@stat.psu.edu] Sent: 28 February 2004 05:20 To: michael watson (…
updated 21.8 years ago • michael watson IAH-C
http:> &gt; &gt; Are you asking about creating a snp annotation package for a different &gt; organism? &gt; &gt; Yes how do I include snp annotation package of a different organism ? Thanks kmo &gt; &gt; &gt; &gt; On 11/26/11 11:03, km wrote
and standards setters (and wannabes), brought together in in one 3 ring circus by the O'Reilly organization, the people who document Open (and some closed) Source IT with their retro-animal covered screeds on Perl, Python...I did attend the 2002 conference, liked most things, didn't like some things, then got hit up by the organizers, to assure more-of-the-former/less-of-the-latter and so have be…
updated 23.0 years ago • Harry Mangalam
<div class="preformatted">Hi, I am trying to build an annotation package starting from Applera Mm array, but I got this strange error running ABPkgBuilder Error in "parser&lt;-"(`*tmp*`, value = "/usr/lib/R/library/AnnBuilder/scripts/llParser4LL") : No direct or inherited method for function "parser&lt;-" for this call Any suggestion? Raffaele (Fedora core 2, R 2.0.0, Bio…
<div class="preformatted">Hi everyone, I'm trying to rebuild my annotation package for an Agilent chip using Resourcerer and it's not finder one of the parsers. The basic error is: &gt;resourcerer2BioC("Agilent_HumanGenome.zip", organism="human") Warning: cannot open file `NA' Warning in unifyMappings(base, eg, ug, otherSrc) : Failed to get or parse Entrez Gene data because …
and flow cytometry. Who we are: Development Sciences (DevSci) is a translational science organization that plays a critical role both in Genentech Research and Early Development (gRED) and late stage development...for contributing to and helping drive data lifecycle management projects that enable the storage, organization, dissemination, and analytics of data in alignment with the scienti…
<div class="preformatted">This is an automated message sent out weekly to report recent changes to Bioconductor packages. Please see the URL http://www.bioconductor.org/changelog.html for a complete history of changes. Unless otherwise noted, these changes apply to the developmental packages only. ---------------------------------------------------------------------- - July 30, 2003 - Met…
updated 22.3 years ago • madman@jimmy.harvard.edu
myBase, srcUrls = mySrcUrls, baseMapType = myBaseType, pkgName = "custommice", pkgPath = myDir, organism = "Mus musculus", version = "1.1.0", author = list(authors = "Yihuan Xu", maintainer = "yihuan.xu at jefferson.edu"), fromWeb = TRUE
_454\_v3.1.1.repeatmasked\_assembly\_v3.0.1.gff3", format = "gff3", dataSource = "Phytozome v12.1", organism = "Sorghum bicolor") then: promoter &lt;- getPromoters(TxDb = Sb\_TxDb, upstream = 2000, downstream = 2000, by = "gene") When I try to
updated 7.7 years ago • sarit.weissmann5
On behalf of the [Bioconductor conference organizing committee](http://bioc2020.bioconductor.org/organizers
updated 5.9 years ago • shepherl
of using GO slims instead of raw (total amount of GOs available in &nbsp;gene universe of the organism of interest) GOs population ? &nbsp;Which pros and cons has each from the mentioned above approaches ?&nbsp
updated 10.2 years ago • s.apocarpum
I am trying to do BLAST (dna-nucleotide) for a sequence. I want to a sequence with the rhesus organism. I would like to get the following values: 1. Score (bits) 2. E-value 3. # Matches I am trying to use the 'annotate' package with
updated 13.3 years ago • Tim Smith
the TSS. I use the below statement for retrieving the 1000 bp upstream region from the TSS for yeast organism. seq=getSequence(id="R0010W",type="ensembl_gene_id",seqType="coding_gen e_flank",upstream=1000,mart = mart); Now my question
updated 15.0 years ago • Kishor Tappita
bam$") &gt; bamfiles [1] "490224.bam" "490225.bam" &gt; rnaSeq &lt;- easyRNASeq(filesDirectory=getwd(), + organism="Hsapiens", + chr.sizes=chr.sizes, + readLength=58L, + annotationMethod="biomaRt", + count="exons", + filenames=bamfiles[1], + …
I'm trying to do pathway analysis for RNA-seq data (KEGG, GSEA, GO). My organism is Bacteroides thetaiotaomicron and I'm having trouble finding an annotation database. AnnotationHub has one...I also tried creating a library using AnnotationForge, which gave me files containing seemingly all organisms and produced an error message: &gt; makeOrgPackageFromNCBI(version = "0.1", + …
updated 5.2 years ago • microPhD
<div class="preformatted">Hi, I would appreciate help with the following. I was following the vignette "How to use AnnBuilder". I tried to adapt this to my goal of creating an annotation data package with the Unigene Identifiers. I made some very minor changes and used the file samclonegb2 which is just a small text file with the first column being a list of IMAGE cloneIDs and the second …
Hi, I've been following the example for using __GOstats__ at its manual at __https://www.bioconductor.org/packages/release/bioc/vignettes/GOstats/inst/doc/GOstatsForUnsupportedOrganisms.pdf.__ Unfortunately I have an error <pre> <em>Error in initialize(value, ...) : invalid names for slots of class “GOHyperGResult”: pvalues, oddsRatios, expectedCounts, catToGeneId, organism</…
updated 9.5 years ago • ccanchaya
Dear All,&nbsp; &nbsp; &nbsp; I am planning to create an annotation package for the organism Heterorhabtidis bacteriophora. I have downloaded all the necessary files of around 85 GB from NCBI using the AnnotationForge
updated 14 months ago • KABILAN
My organization's IT policies have tightened up with regard to making external connections, and I'm getting errors like localHub
updated 4.2 years ago • swbarnes2
file = "Homo_sapiens.GRCh38.105.gtf.gz", format="gtf", dataSource="Ensembl", organism="Homo sapiens") GuitarPlot(txTxdb = txdb, stBedFiles = stBedFiles, headOrtail = TRUE, enableCI = FALSE, mapFilterTranscript
updated 3.8 years ago • 建国
selected to calculate the back ground model, also be promoter sequences of the same(and of the same organism)probes? Regards, Prashantha Hebbar Kiradi, Manipal Life Sciences Center, Manipal University, Email:prashantha.hebbar
updated 15.8 years ago • Prashantha Hebbar
coverage and &gt;90% identity. Is there program in R to select them? I want to detect number of organism showing uniques results for given sequences. &nbsp;Thanks. Dr. Ghorpade Prabhakar B. PhD Scholar ( Veterinary Biochemistry
updated 11.6 years ago • prabhakar ghorpade
Hi I want to use GenomicFeatures to extract upstream sequences from a genome using gene\_IDs My organism (Anopheles melas) has an assembled genome (fasta) and a gtf file. It seems like these are all the files I should need, however
updated 8.2 years ago • david.rinker
command. This is my code spia_result &lt;- spia(de=sig_entrez, all=background_entrez, organism="hsa") head(spia_result, n=5) plotP(spia_result, threshold=0.1) whereas the two vectors are of entrez genes. It all works
updated 5.7 years ago • Assa Yeroslaviz
analysis. But my project is about metatranscriptome. There are many different known and unknown organisms. Is it still possible to do GO enrichment
updated 8.8 years ago • y.zhang36
LAEVIS. For alignment I used mRNA sequence from genebank. Is it possible to do tx2gene for this organism? it is absent here ftp://ftp.ebi.ac.uk/pub/databases/gencode/ and even here https://bioconductor.org/packages/release
updated 6.3 years ago • Daria
package does not seem to have a method to create it from GFF. (we work with non model organisms, so no ucsc/biomart available for us). I should be able to create it with 'makeTranscriptDb(transcripts, splicings
attempting to use the GOstats package to do a differential KEGG pathway analysis in wheat (non-model organism without an organism package). I'm following the guidelines from GOstats for unsupported organisms [here][1]. The problem
updated 13 months ago • a1869161
Hi, I am using the topGO package and this is my code: <pre> # input data head(dat) ID Entrezid Ensembl logFC AveExpr t P.Value adj.P.Val B fc ctrl 1 17500195 20845 ENSMUSG00000031574 1.350722 8.794343 35.00267 3.322001e-09 2.994419e-05 11.46955 2.550397 8.148782 2 17514553 17394 ENSMUSG00000005800 1.474257 7.718298 34.…
updated 10.4 years ago • komalr
1,253 results • Page 7 of 21
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