1,253 results • Page 13 of 21
prob, author = "Javier",email = "email",biocViews = "AnnotationData",genomebuild = "NCBI Build 36",organism = "Human", species = "Homo Sapiens",url = "") makePdInfoPackage(seed, destDir = ".") And I installed the package: R CMD INSTALL pd.hugene.1.0.st.v1
308", "317", "321", "506", "540", "378", "388", "396") > clusterSim(cluster1, cluster2, ont="MF", organism="human", measure="Wang") Error in sqliteExecStatement(con, statement, bind.data) : RS-DBI driver: (expired SQLiteConnection
updated 12.1 years ago • Guest User
Hi, I was using BSseq package to detect DMRs in non-human organism (chicken), I have a few questions that have confused me for some time: 1. The BSseq package reference manual states that
updated 9.1 years ago • Stephen
latest) I've been working with the `biomaRt` package to get mappings between different organizations and I noticed something that, to me, seems like a bug, but I'm not sure. I'm trying to get mappings between `ensembl_gene_id
updated 6.4 years ago • matrs
<div class="preformatted">Dear list, I'm trying to retrieve protein orthologs for human proteins for the most common model organism (mouse,C.elegans,Drosophila,S.cerevisae,etc) such that for my work in human I can point other researchers to the appropriate...Dear list, I'm trying to retrieve protein orthologs for human proteins for the most common model organism (mouse,C.elegans,Drosophila,…
updated 14.8 years ago • Stefanie Carola Gerstberger
gt; library(SPIA) &gt; data(colorectalcancer) &gt; res&lt;-spia(de=DE_Colorectal, all=ALL_Colorectal, organism="hsa",pathids=c("05210","04010"),nB=2000) &gt; res It will take a day or two before the change in the SPIA package will be reflected
<div class="preformatted"> BioConductor Developer Workshop 24 - 25 April 2008 Lausanne, Switzerland This meeting is aimed at active developers as well as prospective developers interested in improving package writing skills and contributing to the BioConductor project. The workshop will be held at the University of Lausanne, Switzerland, with English as the working language. Registration…
updated 18.0 years ago • Darlene Goldstein
GeneGA(sequence=seq,popSize=40,iters=150,crossoverRate=0.3,mutationChance=0.05,region=c(1,60),organism="ec",showGeneration=FALSE)</p> <p abp="297">The error message, produced by the last line of code, is:</p> <pre abp="298"> Error in system
updated 6.5 years ago • chulmelowe
Hi guys,&nbsp; I've been back and forth on this with all sorts of variations, but error keeps coming up. Basically trying to create a geneLists for analysis for clusterprofiler. My numeric are Fisher's P.values from a meta analysis and the names are Gene Symbols though I did also try ProbeIDs.&nbsp; Any chance you know why I'm getting the data.frame error. Oh I check manually if there w…
updated 8.6 years ago • bhgyu
div class="preformatted"> ------ Forwarded Message From: Tabare Mourot <tabare.mourot@igf.cnrs.fr> Organization: IGF Date: Wed, 05 Apr 2006 09:43:22 +0200 To: Sean Davis <sdavis2 at="" mail.nih.gov=""> Subject: Re: [BioC] AnnBuilder package
updated 19.8 years ago • Sean Davis
<div class="preformatted">Hello Bioc users, While our package idiogram is has been created to primarily display gene expression data (with an associated chromLocation object) you can alternatively create one on the fly. In the code below I create a mock data frame similar to Camper's and from that I generate a bare bones chromLocation object. From there you can plot the data a coup…
updated 17.2 years ago • Dykema, Karl
Hello I'm using SPIA on my toptable generated by limma. I have R version&nbsp;3.3.1, and updated biocLite to the latest version. It makes the results file using&nbsp; res=spia(de=DE,all=ALL,organism="hsa",nB=2000,plots=FALSE,beta=NULL,combine="fisher") However, when I use plotP(res,threshold=0.05) I get the following error...biocLite to the latest version. It makes the results file u…
updated 9.1 years ago • docpriya21
a single column of transcript names for Arabidopsis thaliana using our internal "orgid" filter for organism ID 167: &gt; library('biomaRt') &gt; phyto=useMart('phytozome_mart', dataset='phytozome') &gt; transcripts = getBM(attributes
paper submission For more information, please visit http://www.camda2009.org Sincerely, CAMDA2009 organizers [[alternative HTML version deleted]] </div
updated 16.4 years ago • Pan Du
a 2 x 2 x 2 factorial arrangement. Objective: Compare the differences in gene expression in each organ (HG or TC) within each timepoint (24 or 48). For that, analyze main factors interactions or if they act together on each gene...in each organ/timepoint. edgeR approach used: Experiments with all combinations of multiple factors The groups: ``` [1] CM.14.NO CM.14.NO
updated 22 months ago • tsl0026
TRUE/FALSE needed In addition: There were 11 warnings (use warnings() to see them) &gt; gpQuality(organism = "Hs") [1] "Starting gpQuality..." Error in if (abs(MMR[i]) &gt; 0.5) numSpotOverMmrLim &lt;- numSpotOverMmrLim + : missing value where...gt; traceback() 2: slideQuality(gp, controlMatrix = controlMatrix, DEBUG = DEBUG) 1: gpQuality(organism = "Hs") &gt; warnings() Warnin…
updated 11.4 years ago • Guest User
hub &lt;- AnnotationHub:::AnnotationHub() ## Query for the specific database (organism &amp; sqlite) query_result &lt;- AnnotationHub:::query(hub, c("Heterorhabditis", "bacteriophora", "sqlite")) ## Assuming the SQLite
and GFF files). So, I'm doing this: ``` txdb &lt;- makeTxDbFromGFF (file = GFF_FN, dataSource="...", organism="Saccharomyces cerevisiae") seqinfo &lt;- Seqinfo (seqnames = c(...), seqlengths=c(...), isCircular=c(...), genome="..") vcf &lt;- readVcf (VCF_FN
updated 3.3 years ago • rwan.work
ALL",pvalueCutoff = 0.05,qvalueCutoff = 0.05, readable = T) KEGG&lt;-enrichKEGG(gene$ENTREZID,organism = KEGG_database,pvalueCutoff = 0.05,qvalueCutoff =0.05) barplot(KEGG,showCategory = 30,title = 'KEGG Pathway') barplot
updated 4.0 years ago • waltsonwang88
Program Committee: Robert Gentleman, Darlene Goldstein, Wolfgang Huber, Victor Jongeneel Local Organizer: Darlene Goldstein Sponsors: Hewlett-Packard and Intel -- Darlene Goldstein ?cole Polytechnique F?d?rale de Lausanne
updated 18.9 years ago • Darlene Goldstein
be very useful to be able to be able to deal with values that are greater than 2^32 (≈ 10^9) as many organisms have genome size longer than that. __Question__ - Am I right to think that this is an integer overflow issue? - Do you
updated 9.8 years ago • remi.b.md
<div class="preformatted">Dear all,* * enrollment is open for 4 PhD positions in cancer computational biology at the IFOM-IEO campus in Milan, see the ad below. Best, mattia ** *############################# * * * *Cancer computational biology* Four PhD positions in Computational Biology are available at the IFOM- IEO Campus in Milan. The candidates will have the opportunity to wor…
nbsp; &nbsp;0.000 &nbsp; &nbsp;7.597 &nbsp; &nbsp;5 &nbsp; &nbsp;30 &nbsp; &nbsp;789 &nbsp; &nbsp;organ morphogenesis Which test genes (entrez ids) were present in 'tissue developemnt'? Is&nbsp;is possible? Thanks in Advance
updated 11.0 years ago • Bade
<div class="preformatted">Hi, Aric, I moved the conversation here because other people might be benefit from it. Similar to rangeGate() and quandrantGate(), an extra argument 'plot' is added to lymphGate() to produce plots of filter results. This update is included in flowStats V 1.7.4 in the Bioc-devel branch. -------- Original Message -------- Subject: Re: flowStats update ?ly…
updated 15.5 years ago • Chao-Jen Wong
1235745522981523457?s=20 ## English version (en inglés) ``` Do you want to learn how to organize your R code 👨🏽‍💻 and analyze 👩🏽‍💻single cell RNA sequencing data with @Bioconductor? Save the date! See you August 3-7 🗓 Instructors
updated 5.8 years ago • Leonardo Collado Torres
Please circulate widely. UC Irvine's newly created Research CyberInfrastructure Center (RCIC) is seeking a Director to oversee it's growth and increasing influence in supporting research via digital services. The RCIC will serve as the central resource for accessing, providing, coordinating and enhancing research Information Technology facilities and services for the University of California, I…
updated 8.5 years ago • hjmangalam
factor activity nucleus Probe Set ID 220184_at GeneChip Array Human Genome U133 Plus 2.0 Array Organism Common Name Human Probe Design Information Transcript ID g13376297 Sequence Type Exemplar sequence Representative
<div class="preformatted">I am trying to make annotation package for my array platform using AnnotationDbi package. I prepared txt file that links customID and unigene. The table I am trying to import here has only 2 columns; one is gene id (CLIGG_00001) and the other is unigene id (Gga.1). I tried all I could google out and many as.character or bimap options...Here is the R output: &…
updated 14.8 years ago • Dana.Stanley@csiro.au
booklet\_advance\_RNAseq\_2015.pdf Registration deadline April the 1st 2015 The Organizer Raffaele A Calogero &nbsp; ---------------------------------------- Prof. Raffaele A. Calogero Bioinformatics and Genomics Unit MBC Centro di Biotecnologie
updated 11.0 years ago • raffaele calogero
<div class="preformatted">Hi All I am trying to build an annotation library for some in-house plant microarrays using AnnBuilder. I have a base file that consists of a column of probe names, and nearest matches to NCBI genes. I have installed entrex files, unigene files and go files locally to speed the process. I am trying to map the plant probes on the microarray to rice genes in UniG…
use GSEABase to accomplish this. Oh, one last thing to add, all of our work is with non-model organisms with limited/non-existent genomic resources. So, I do have UniProt IDs associated with these gene/transcript IDs
updated 5.9 years ago • samwhite
mySrcUrls, baseMapType = myBaseType, otherSrc = myOtherSrc, pkgName = "myPkg", pkgPath = myDir, organism = "Homo sapiens", version = "1.1.0", author = list(authors = "myname", maintainer = "myname at myemail.com"), fromWeb = TRUE) I result
updated 19.0 years ago • Martin Kircher
of googling around. That's what I've done so far: countTable &lt;- easyRNASeq(filesDirectory=getwd(), organism="Hsapiens", annotationMethod="rda", annotationFile="gAnnot.rda", gapped=TRUE, count="genes", summarization="geneModels...of 51 bp. [...] Preparing output Wa…
<div class="preformatted">hi all, I'm building a custom annotation service, and have encountered the following problems. Upon Reading the SQLForge.pdf vignette, i decided that i would not choose to use these functions popHUMANCHIPDB populateDB but instead build my own SQLite Database following the Database Schema Version 1.0 described in AnnotationDbi/inst/DBschemas/schemas_1.0/HUMANCH…
DBSCHEMAVERSION: 2.1 | Db type: OrgDb | Supporting package: AnnotationDbi | DBSCHEMA: RAT_DB | ORGANISM: Rattus norvegicus | SPECIES: Rat | EGSOURCEDATE: 2015-Aug11 | EGSOURCENAME: Entrez Gene | EGSOURCEURL: ftp://ftp.ncbi.nlm.nih.gov...DBSCHEMAVERSION: 2.1 | Db type: OrgDb | Supporting package: AnnotationDbi | DBSCHEMA: RAT_DB | ORGANISM: Rattus norvegicus | SPECIES: Rat | EGSOURCE…
updated 9.3 years ago • Jenny Drnevich
actually all the genes in my transcriptome since I used the same data to assemble it) - since my organism is not supported by GOseq, I created a vector with gene lengths from tximport count matrix with ```lengthData &lt;- rowMeans
updated 3 months ago • f
design and interpretation of disease transcriptomics and genome sequences in humans and model organisms. Building your career together with a cohesive, interactive team of highly experienced bioinformaticians, you
updated 8.1 years ago • Mark Dunning
vary across clinical categories. 4. Are there recurrent sequences that do not align to known organisms for a particular cancer type. This will give the intriguing possibility of discovering brand new bacteria that
updated 8.8 years ago • Daniel Brewer
Description.Full.genome.sequences.for.Rhinella.marina..cane.toad..as.provided.by.UNSW..RM170330.. 1 organism:Rhinella marina 2 Description.Full.genome.sequences.for.Rhinella.marina..cane.toad..as.provided.by.UNSW
updated 5.3 years ago • jiazhou0116
K_geneID)) %&gt;% pull(K_geneID) %&gt;% as.character() %&gt;% enrichKEGG(gene=., organism="ko", universe=koalaList$K_geneID) enriched@result %&gt;% as.tibble() %&gt;% dplyr::select(-geneID) %&gt;% arrange(desc(Count)) ID Description
updated 6.2 years ago • lindseypieper
annotation gff file (or similar), for a genome that is not included in the UCSC catalog of reference organisms (as is the case of this bacteria I have to analyze)? Thanks in advance JL PD. I came across "Rsubread" package, but... package
1: multiple methods tables found for ‘fileName’&nbsp; 2: multiple methods tables found for ‘organism’" and when I use "&nbsp;__DESeqDataSetFromMatrix__" function, I get this error message: "__Error in slot(value, what) :&nbsp
updated 7.6 years ago • nazaninhoseinkhan
diet), I need to adjust for age, sex and possibly body mass index. That is an example of my data organization ``` Sample ID Timepoint Metabolite change_metabolite Sex Age BMI 1a 1 1 10,3000 0,0000 1 56,5 38,1 1b 1 2 20,1000 9,8000
updated 5.3 years ago • anna.cot.anna.cot
makeTxDbFromGFF("/home/inah/MESA\_mRNAseq\_New/gencode.v28.long\_noncoding\_RNAs.gtf", format="gtf",organism="Homo sapiens") exons.list.per.gene &lt;- exonsBy(txdb,by="gene") exonic.gene.sizes &lt;- lapply(exons.list.per.gene
updated 7.6 years ago • Ina Hoeschele
to add "ORF IDs to Chromosomal Location" to my data frame named genes in the DGEList-object. The organism is yeast, and I downloaded org.Sc.sgd.db.. ``` &gt; columns(org.Sc.sgd.db) [1] "ALIAS" "COMMON" "DESCRIPTION" "ENSEMBL" "ENSEMBLPROT...Number of mapped keys for the maps in package org.Sc.sgd.db org.Sc.sgdORGANISM The Organism for org.Sc.sgd org.Sc.sgdPATH …
updated 2.1 years ago • Chih
combinations. While the four types of controls are basically the same strain/species of untreated organisms, they came however from different batch of lab organisms in different season/year so are likely different to some
updated 12.9 years ago • RLW
combinations. While the four types of controls are basically the same strain/species of untreated organisms, they came however from different batch of lab organisms in different season/year so are likely different to some
updated 12.9 years ago • RLW
is going to be difficult, because there are many different annotation formats and many different organisms specificity. It is very frequently necessary to make custom annotations because users have different questions...you are seeing above is telling you. To decide whether this is critical or not depends on your organisms and on the cases where these occur; e.g. in drosophila, poplar, these are …
Thanks! ```r &gt; forgeBSgenomeDataPkgFromNCBI(assembly_accession="GCA_002863925.1", + organism="Equus caballus") Error in find_NCBI_assembly_ftp_dir(assembly_accession, assembly_name = assembly_name) : unable
Hello, Can someone help me to subset each first intron (only) from a GRangesList representing intronsByTranscript? I've been somewhat out of practice for a period of time, and I'm stuck. Thanks, ``` tx TxDb object: # Db type: TxDb # Supporting package: GenomicFeatures # Data source: GCA_007735645.1 # Organism: Venturia.effusa # Taxonomy ID: 50376 # miRBase build ID: NA # Genome: ASM773564v1 #…
updated 23 months ago • mat149
lt;- df2$log2FoldChange kegg_organism = "ath" kk2 &lt;- gseKEGG(geneList = kegg_gene_list, organism = kegg_organism, nPerm = 10000, minGSSize = 3, maxGSSize = 800, pvalueCutoff = 0.05, pAdjustMethod = "none", keyType = "ncbi-geneid
reconstructed metabolic networks will improve insight in the molecular functioning of a cell or an organism. Moreover, such networks might reveal disease progression, efficacy of treatments, effects of interventions and
mailing list. I'm trying to use ChIPpeakAnno to identify the annotation of ChIP-Seq peaks for an organism that does not have an annotation package. I have used makeTranscriptDbFromGFF to create a transcriptDb object
Andrew Beggs", email = "a.beggs at bham.ac.uk", biocViews = "AnnotationData",genomebuild = "HG 18", organism = "Human", species = "Homo Sapiens", url = "http://www.biostat.jhsph.edu/~bcarvalh") makePdInfoPackage(seed, destDir = ".") -- output
I am working with __MEDIPS__ bioconductor. I was able to successfully create a custom BEE genome (I know its already there in MEDIPS, but for some reason I wanted to make a different one myself). The genome folder consists of 16 separate fasta files for each chromosomes named like chr1, chr2 and so on. The seed file is given below: <pre> Package: BSgenome.Amellifera.UCSC.apiMe1 Title: …
updated 9.1 years ago • Vijay Lakhujani
myBase, srcUrls = mySrcUrls, baseMapType = myBaseType, pkgName = "custommice", pkgPath = myDir, organism = "Mus musculus", version = "1.2.0", author = list(authors = "Yihuan Xu", maintainer = "Yihuan XU <yihuan.xu at="" jefferson.edu="">"), fromWeb
Author = author, Maintainer = maintainer, PkgTemplate = "ORGANISM.DB", AnnObjPrefix = dbName, organism = paste(genus, species), species = paste(genus, species), biocViews = "annotation", manufacturerUrl = "no manufacturer", manufacturer
are no mismatch probes. We estimate background with a subset of probes that target a very different organism and are essentially negative controls. These 'background' probes are randomly distributed so they broadly sample
updated 19.1 years ago • Wolfgang Huber
pre> # Db type: TxDb # Supporting package: GenomicFeatures # Data source: test.gff3 # Organism: NA # Taxonomy ID: NA # miRBase build ID: NA # Genome: NA # transcript_nrow: 17660 # exon_nrow: 66022 # cds_nrow: 62514 # Db created
http://www.bioinformatica.unito.it/RNAseq.course.html or contact : raffaele.calogero@unito.it The Organizer Raffaele Calogero -- ---------------------------------------- Prof. Raffaele A. Calogero Bioinformatics and Genomics Unit MBC Centro di Biotecnologie Molecolari
updated 12.0 years ago • raffaele calogero
1,253 results • Page 13 of 21
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