1,253 results • Page 12 of 21
URGI; v1a) see https://urgi.versailles.inra.fr/Species/Pisum/Pea-Genome-project Version: 1a organism: Pisum sativum common_name: Pea genome: Pisum_sativum_v1a provider: URGI provider_version: Pisum_sativum_v1a
updated 5.0 years ago • sophie.harrington
kgml.path="C:\\Users\\David\\Documents\\R\\win-library\\3 .0\\SPIA\\extdata\\keggxml\\hsa",organism="aag",out.path="C:\\Users\\D avid\\Documents\\R\\win-library\\SPIA\\extdata\\") This resulted in [1] TRUE and an aagSPIA.RData file
updated 12.0 years ago • David Price
sequences for Zea mays (AGPv3) Description: Full genome sequences for Zea mays Version: 1.0.0 organism: Zea mays common_name: maize provider: NCBI provider_version: release_date: Oct. 2015 release_name: MaizeGDB source_url
updated 10.3 years ago • Marcin Grzybowski
<div class="preformatted">Dear all, Now I am using pathview to map my RNAseq expression data to the keggmap of my organism 'mez'. I want to know how pathview deal with the colour of enzyme with several conding genes, for example: In pathway: Glycolysis...Dear all, Now I am using pathview to map my RNAseq expression data to the keggmap of my organism 'mez'. I want to know how pathview dea…
GOSemSim package, but I am getting the following error: &nbsp; __&gt; mgeneSim(protein\_id\_list, organism="human")__ &nbsp; &nbsp; &lt;0 x 0 matrix&gt; &nbsp; &nbsp; There were 50 or more warnings (use warnings() to see the first 50) __&gt; warnings
updated 9.7 years ago • ረ
## __New: Master of Science (Laurea Magistrale) in Quantitative and Computational Biology__ ### ___University of Trento, Italy___ a&nbsp;__multidisciplinary degree that formally integrates quantitative sciences and applied biology__, thanks to the following organizations at the University of Trento: * <a href="http://www.cibio.unitn.it/" target="_blank">CIBIO, Centre for integrativ…
<div class="preformatted">Dear Bioconductor Developers and Users, I have created few annotation packages which are for organism specific proteomics database from IPI(http://www.ebi.ac.uk/IPI/IPIhelp.html) . Now I am keen on writing a generic utility...Dear Bioconductor Developers and Users, I have created few annotation packages which are for organism specific proteomics database from…
<div class="preformatted">Hi all, actually, I have (a) similar question(s) regarding a very non- standard Agilent data set: this is a custom 60mer oligo chip, the probes of which are designed from Arabidopsis thaliana sequence information, but intended to measure expression in the related non-model organism Arabis alpina. There are several probes per A. thaliana gene (not always the same…
are revolutionizing genetics by allowing us to sequence the genomes of many different individual organisms in a population and to observe their complex coding and non-coding transcriptomes and regulatory events under
gt; ABPkgBuilder(baseName=myBase,srcUrls=mySrcUrls,baseMapType="ll", + pkgName="rats",pkgPath=myDir,organism="Rattus norvegicus",version="1.1.0", + author=list(authors="Alice",maintainer="alice.johnstone at esr.cri.nz"),fro mWeb...baseName = myBase, srcUrls = mySrcUrls, baseMapType = "ll", pkgName = "rats", pkgPath = myDir, organism = "Rattus norvegicus", version = "1.1.0", author =…
updated 18.1 years ago • Johnstone, Alice
Hi everyone, I have problem in reproducing vignette example from MeSHDbi package. That is, when I run: <pre> &gt; example("makeGeneMeSHPackage")</pre> It should use &nbsp;preformatted data frames "PAO1" and "metaPAO1" to construct custom org.MeSH.XXX.db package that can subsequently be loaded via library() and queried with Annotation.dbi or RSQLite, or at least that is ho…
updated 10.8 years ago • Ceca Bojic
249") # Pathway enrichment analysis enriched_pathways &lt;- enrichPathway(gene = random_genes, organism = "mouse") # Extract pathway and gene information pathways &lt;- as.data.frame(enriched_pathways) `# Create an edge list
updated 18 months ago • Antonio
0.01, qvalueCutoff = 0.05) ``` returning: ``` # # over-representation test # #...@organism Homo sapiens #...@ontology BP #...@keytype SYMBOL #...@gene chr [1:294] "SORBS1" "PIK3C3" "TBC1D4" "SKP2" "PELI1" "SCIN" "LPL" "SPOPL" "BRAF" "SIRT1
updated 4.1 years ago • samsiljee
indexDir = "/Users/atari/biodata/genomes/ensembl_hg38/indexes/SALMON", source = "ensembl", organism = "Homo Sapiens", release = 98, genome = "GRCh38", fasta = "/Users/atari/biodata/genomes/ensembl_hg38/transcripts/ensembl_hg38_transcripts.fa.gz
updated 4.1 years ago • atariw
have done RNAseq and the usual differential gene expression analysis pipelines (Deseq, etc) in one organism under two different conditions and now, we would like to do it between these different bacteria. We have 2 different
Y and M. What is chr4_gl000193_random for instance. Thank you #========= Hsapiens Human genome | | organism: Homo sapiens (Human) | provider: UCSC | provider version: hg19 | release date: Feb. 2009 | release name: Genome Reference Consortium
Loading required package: RCurl Loading required package: bitops extracting only data for our organism from : gene2pubmed Getting data for gene2accession.gz Error in sqliteSendQuery(con, statement, bind.data) :&nbsp
txdb TxDb object: # Db type: TxDb # Supporting package: GenomicFeatures # Data source: BioMart # Organism: Saccharomyces cerevisiae # Taxonomy ID: 4932 # Resource URL: www.biomart.org:80 # BioMart database: ensembl # BioMart
updated 10.2 years ago • vinod.acear
from well-controlled experiments are 0.4 for human data, 0.1 for data on genetically identical model organisms or 0.01 for technical replicates. " But I came across this post which mentions a conservative way to calculate BCV
updated 12.0 years ago • Bade
clusterProfiler) &gt; data(gcSample) &gt; xx &lt;- compareCluster(gcSample, fun="enrichKEGG", + organism="hsa", pvalueCutoff=0.05) &gt; p1 &lt;- emapplot(xx) Fehler in (function (classes, fdef, mtable) : unable to find an inherited method
<div class="preformatted">I regret that I must announce the cancellation of the course announced below, owing to logistic difficulties and low turnout for this particular date. When the course is rescheduled, it will be announced on this list. On Tue, Sep 17, 2013 at 1:10 AM, Vincent Carey <stvjc@channing.harvard.edu>wrote: &gt; This two day course is described in a preliminary…
updated 12.3 years ago • Vincent J. Carey, Jr.
Hi all,&nbsp; I was just wondering if somebody could help me regarding normalized count after DESeq. I carry out a DESeq on a time course experiment in order to then make a count matrix of significantly expressed genes to look for patterns in gene expression across different samples. However, I have noticed that the count matrix I am making post DESeq on significantly expressed genes are ac…
updated 7.7 years ago • A
2.1 | Db type: ChipDb | Supporting package: AnnotationDbi | DBSCHEMA: HUMANCHIP_DB | ORGANISM: Homo sapiens | SPECIES: Human | MANUFACTURER: Affymetrix | CHIPNAME: Human Genome U133 Set | MANUFACTURERURL: http://www.affymetrix.com
updated 7.8 years ago • Agaz Hussain Wani
2, ..., 10 (total: 10) geneIdType: Null collectionType: Null setIdentifier: MyId description: organism: pubMedIds: urls: contributor: setVersion: 0.0.1 creationDate: &gt; c(setName(myGset), setIdentifier(myGset)) ; [1] "MyName...Null setIdentifier: bdmgWorkstation2:28927:Tue Jan 24 12:09:13 2017:1 description: organism: pubMedIds: urls: contributor: …
updated 8.9 years ago • jcrodriguez
of FC values in each condition separately. <pre> &gt; viewPathway("Scavenging by Class B Receptors", organism = "human", readable = TRUE, foldChange = cond1FC, vertex.label.font = 3, vertex.label.cex = 0.7, col.bin = 10, legend.x = 1, legend.y...columns</pre> http://imgur.com/w77zQO4 <pre> &gt; viewPathway("Scavenging by Class B Receptors", organism = "human", reada…
updated 9.0 years ago • Kajus Baidžajevas
notes)) { cat("Generating notes from ", fnames[1], "\n", sep="") row &lt;- grep("Organism", y)[1] organism &lt;- strsplit(y[row], "=")[[1]][2] row &lt;- grep("Category", y)[1] category &lt;- strsplit(y[row], "=")[[1]][2] row &lt;- grep("Subcategory", y)[1] subcategory...collapse = ",") else parameter…
REVIGO website for some reason, I've been trying to use rrvgo package. I'm working with a non-model organism, so I used Blast2GO to annotate the sequences and obtain their associated GO terms. Also, I created an OrgDbPackage
updated 14 months ago • daccar98
Hsapiens, chrs="chr21", width=250, spacing=250) &gt; cpgdens &lt;- cpgDensityCalc(windows, organism=Hsapiens, w.function="linear", window=700) &nbsp; &gt; sI &lt;- matrix(rnbinom(2\*length(windows), mu=5, size=2), ncol=2) &gt; bm &lt;- BayMethList
updated 10.4 years ago • Matthias Lienhard
and that you provide me the list of exon level probe sets you are trying to plot and which organism you are using. Cheers Raffaele -- ---------------------------------------- Prof. Raffaele A. Calogero Bioinformatics and Genomics Unit Dipartimento di Scienze
<div class="preformatted"> Call for Contributions ===================================================================== LIFE SCIENCE FREE SOFTWARE SESSION held at CompLife 2006 (http://www.complife.org) in Cambridge, United Kingdom, on September 27 - 29, 2006 ===================================================================== In the l…
updated 19.6 years ago • Thorsten Meinl
Hi Bioconductor Support, Since 2018 I've been interacting with rOpenSci's organizers. For those that don't know, [rOpenSci](https://ropensci.org/) is a non-profit that aims to &gt; make scientific data retrieval
updated 5.8 years ago • Leonardo Collado Torres
<div class="preformatted">Hi, I get the "Error in pathIDsLev1" error when using the gene2pathway retrain() function. &gt; retrain(minnmap=30, level1Only="Metabolism", level2Only="Genetic Information Processing", organism="hsa", gene2Domains=NULL, KEGG.package=TRUE, remove.duplicates=FALSE, use.bagging=TRUE, nbag=11) Retrieving KEGG information...gt; retrain(minnmap=30, level1Only="Met…
updated 16.1 years ago • Dick Beyer
but the result is in line with the current knowledge of sex-biased gene expression in my model organism. I have done some quality control plots, available here: - Boxplot: http://www.iee.uu.se/zooekol/pdf/hemiarray_qc_boxplot.pdf
updated 16.7 years ago • Paolo Innocenti
step is for CEOs and other business leaders to recognize the strategic role that IT plays within an organization. We all know and love normal radio. uk - Save Internet Radio. </div
updated 18.5 years ago • Charlie
<div class="preformatted">Hi, Hope you're fine I am trying to make whole genome plots using the geneplotter package/annotate package. The organism I am studying is Arabidopsis thaliana, and obviously the annotations are not so extensive there: when trying to build...re fine I am trying to make whole genome plots using the geneplotter package/annotate package. The organism I am studying i…
updated 17.2 years ago • Samuel Wuest
<div class="preformatted"> Hi, I have a question regarding the minimal number of genes that we can test in an analysis with edgeR. Let me explain, in a study, edgeR have been used for testing the differential expression of three viruses between two conditions, without considering the counts on other features. That is, the data frame d$counts has only three lines (and 4 columns, as there i…
updated 13.2 years ago • Guest User
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 …
looks great. Would that we had such a resource (curated, &gt; current, and growing) for all organisms! &gt; &gt; A few questions, if I may: &gt; &gt; 1) What role with respect to FlyFactorSurvey do you picture us taking here &gt; at...policy? &gt; &gt; 4) Is TRANSFAC only for license holders? &gt; &gt; 5) Are there any other organism-speci…
updated 13.7 years ago • Vince Schulz
to study the functional (expression) evolution of mammalian genomes across gene types, lineages, organs, cell types, developmental stages, chromosomes and sexes. The postdoctoral fellow will be funded by a recently awarded...R., Paabo, S., and Kaessmann, H. (2011) The evolution of gene expression levels in mammalian organs. Nature 478: 343-348. &nbsp
updated 9.8 years ago • henrik.kaessmann
myBaseType, + + otherSrc = myOtherSrc, pkgName = "myPkg", pkgPath = myDir, Error: syntax error &gt; + organism = "Homo sapiens", version = "1.1.0", makeXML = FALSE, Error: syntax error &gt; + author = list(author = "myname", maintainer = "myname at...mySrcUrls, baseMapType = myBaseType, + otherSrc = myOtherSrc, pkgName = "myPkg", pkgPath = myDir, + organism = "Homo sapiens", version = "1.…
I have some general questions about doing a time series RNA-seq experiment. The RNA is from a non-model organism. The experiment has no conditions for comparison (so just the "control" condition, essentially). Three biological replicates...some general questions about doing a time series RNA-seq experiment. The RNA is from a non-model organism. The experiment has no conditions for compariso…
updated 3.0 years ago • Dunois
# Group Greeting Cards in R Are you looking for a fun and personalized way to celebrate a special occasion with a group of friends, family, or colleagues? Group greeting cards in R might be the perfect solution! With R's powerful data manipulation and visualization capabilities, you can create custom greeting cards that include messages and images from multiple contributors. Here's how it w…
updated 2.4 years ago • carterethan745
Genomics Research (CGR) laboratory in Gaithersburg, MD, is an advanced, fast-paced, high-throughput organization dedicated to the support of molecular, genetic and epidemiologic studies for investigators at the National
updated 2.9 years ago • Wendy
Hello! I have a list of about 6400 differentially expressed genes and I want to perform KEGG pathways enrichment analysis using the clusterProfiler package. I first did it with the ORA method, using the `enrichKEGG` function and doing it separately on the genes with positive and negative logFC. I got hundreds of enriched pathways with this method, both for the up and downregulated genes. I then…
updated 4.9 years ago • Emilia
I have, it seems to be working fine for all except for one dataset. This dataset is from the organism fly while the others are either mouse or human.When I&nbsp; run deseq2 with 'LRT' for the fly dataset I get the following
updated 9.2 years ago • szenitha
Hi I have RNA seq data for six different treatments (A,B,C,D,E,F) of a model organism, with four-fold biological (NOT technical) replicates. FASTQC revealed no abnormalites in the RNAseq data and after
analysis using enrichGO function through clusterProfiler. As I am going to analyze nonmodel organism seabream so I used AnnotationHub to build OrgDb. I retrieved the annotation database library(AnnotationHub) hub
baseName = "GEM.txt", srcUrls = mySrcUrls, baseMapType =myBaseType, pkgName = "GEM",pkgPath = myDir, organism = "Mus musculus", version = "1.0.0",author = list(authors = "joe", maintainer ="joe.joe at gmail.com"), fromWeb = TRUE) after the creation
MoGene data collected for mouse using the following command: res = spia(de = DE, all = ALL, organism = "mmu", nB = 2000, plots = FALSE, beta = NULL) The procedure runs to completion and produces results and shows several pathways
but as far as we are able to understand the packages use the info available in the corresponding organism .db0 packages. However, it is not clear to us how now to continue with the mirna.db SQLite file we created. Any advice
with only one ORF sequence per gene. P.P.S. Alternative splicing isn't a consideration for this organism
updated 7.6 years ago • andrewpountain
Analyst The EMMES Corporation, organized in 1977, is a privately owned Contract Research Organization (CRO) located in Rockville, Maryland. EMMES is dedicated to providing statistical and epidemiological expertise
updated 17.2 years ago • Marcella Pickard
Hello, I have been conducting pathway analysis on my RNA-seq data using the Deseq2/GAGE workflow. I ran GAGE and it worked well generating a list of affected pathways. I used “KO” annotations from kegg.gsets (species=”ko”) as I am working on a non-model organism. I am now trying to extract data for essential member genes in my perturbed pathways with essGene() However, I keep getting...pathways.…
updated 9.2 years ago • Michael
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 12.7 years ago • wang peter
baseName=myBase, srcUrls=mySrcUrls, baseMapType=myBaseType, pkgName="PRG_protein_pkg", pkgPath=myDir, organism="Oryza sativa", version="1.1.0", author=list(author="Ross", maintainer="ross.chapman at xxxxxxxx"), fromWeb=FALSE)} date() Can
2) Make sure you have have the appropriate BSgenome.* package which has the genomic sequence for the organism you are working with. For instance, if you are working with human data with the hg19 release, you'd need the BSgenome.Hsapiens.UCSC.hg19
most people expect. And the pig org package is made (special) here along with all the other major organism packages that we support. It is not generated by the method you used because that method has to work for ALL organisms...not meant to be a way to get a newer package. It is meant to allow people who are using non-model organisms to get annotations. So it is expected that some things are …
Chromosome names of query and genome do not match &gt; head(BSgenome,100) 1 function (organism, common_name, genome, provider, provider_version, 2 release_date, release_name, source_url, seqnames, circ_seqs...seqinfo) 11 if (missing(common_name)) 12 common_name &lt;- species 13 metadata &lt;- list(organism = organism, common_name = common_name, 14 genome = ge…
updated 3.9 years ago • alexandre.maucuer
function calls ... OK * checking R code for possible problems ... NOTE .onLoad: warning in BSgenome(organism = "Saccharomyces cerevisiae SK1", species = "Yeast", provider = "Hochwagen Lab", provider_version = "1.00", release_date = "Unsure...extdata_dir): partial argument match of 'seqs_dir' to 'seqs_dirpath' .onLoad: warning in BSgenome(organism = "Saccharomyces cerevisiae SK1", species …
_Down") &nbsp; CompKEGG\_limma &lt;- compareCluster(geneCluster = list\_limma, fun = "enrichKEGG",organism="hsa", pvalueCutoff=1) CompKEGG\_edge &lt;- compareCluster(geneCluster = list\_edge, fun = "enrichKEGG",organism="hsa", pvalueCutoff...1) CompKEGG &lt;- compareCluster(geneCluster = list, fun = "enrichKEGG",organism="hsa", pvalueCutoff=1) &nbsp
updated 8.5 years ago • joseph
1,253 results • Page 12 of 21
Traffic: 1611 users visited in the last hour
Help About
FAQ
Access RSS
API
Stats

Use of this site constitutes acceptance of our User Agreement and Privacy Policy.

Powered by the version 2.3.6