1,253 results • Page 11 of 21
lt;-scan(genes,character()) Read 97 items > gs<-GSEABase::GeneSet(geneIds=inputGenes,organism='Homo Sapiens', + geneIdType=GSEABase::SymbolIdentifier()) > output<-teEnrichment(gs) Error in teEnrichment(gs) : could...lt;-scan(genes,character()) Read 97 items > gs<-GSEABase::GeneSet(geneIds=inputGenes,organism='Homo Sapiens', + …
updated 4.2 years ago • sarvesh.nikumbh
ago. So at the time I downloaded the ds_flat_ch*.flat files from here ftp://ftp.ncbi.nih.gov/snp/organisms/human_9606/ASN1_flat in order to build SNPlocs.Hsapiens.dbSNP.20080617 (that was in March 2009), I assume that...these files were a dump from Build 129. Note that the files under ftp://ftp.ncbi.nih.gov/snp/organisms/human_9606/ASN1_flat can change at anytime (and today they are indee…
updated 10.5 years ago • Hervé Pagès
I loaded by using Annotationhub, because my target species "acanthamoeba castellanii" is not a model organism. ``` hub <- AnnotationHub::AnnotationHub() amoeba <- query(hub, "Acanthamoeba castellanii") # title # AH65301 | Acanthamoeba...hub[["AH81410"]] > Acan.OrgDb OrgDb object: | DBSCHEMAVERSION: 2.1 | DBSCHE…
updated 5.6 years ago • Ruixuan
and multi- genome protein motif searches. ? Local establishment and customization of model organism genomic databases (e.g. ENSEMBL) and tools for batch sequence analysis utilizing these resources. ? Perform other...nearly $200 million annually in funding from government agencies, private groups and philanthropic organizations. Faculty members are nationally recognized authorities in a…
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updated 17.2 years ago • Linda Jones
Hi I'm working with non-model organism, doesn't have any information in the public domain. After denovo assembly using trinity for all 32 samples, using...Hi I'm working with non-model organism, doesn't have any information in the public domain. After denovo assembly using trinity for all 32 samples, using salmon...Now, how do i create, tx2gene dataframe, the genome,GTF information is not a…
updated 5.5 years ago • sunnykevin97
genes <- data$Ensembl_Gene_ID genes <- as.character(genes) ggo <- groupGO(gene = genes, organism = "human", ont = "BP", level = 3, readable = TRUE) # Enrich GO genes<-data$Ensembl_Gene_ID[abs(data$log2FC_DeSeq)>2] ego <- enrichGO...genes , organism= "human", ont= "CC", pAdjustMethod="BH", pvalueCutoff=0.1, qvalueCutoff=0.5, readab…
updated 8.8 years ago • Mataivic
AnnBuilder"), "data", "thgu95a") > myBaseType <- "gb" > mySrcUrls <- getSrcUrl("all", organism = "Homo sapiens") > mySrcUrls LL "ftp://ftp.ncbi.nih.gov/refseq/LocusLink/LL_tmpl.gz" GP "http://hgdownload.cse.ucsc.edu...mySrcUrls, baseMapType = g, + pkgName = "myPkg", + pkgPath = myDir, organism = "Homo sapiens", version = "1.1.0", + …
Im a beginner in R and I want to forge Casuarina equistifolia genome in BSgenome package as it is not available as inbuilt package. After spending so much time in solving errors but still I couldn't solve one error. Kindly help me to solve the below error. #Seed File I have used ``` Package: BSgenome.Cequisetifolia.NCBI.ASM379533v1 Title: Full genome sequences for Casuarina equisetifolia incan…
updated 3.4 years ago • Manoj Kumar R
genome = gen, chromosome = chr) #TxDb object txdb <- makeTxDbFromGFF(file="assembled.gtf", organism="Homo sapiens", format = "gtf") #gene track grtrack <- GeneRegionTrack(txdb, genome = gen, chromosome = chr, fill='black', transcriptAnnotation
updated 4.4 years ago • karlaarz
gt; Rhinopithecus OrgDb object: | DBSCHEMAVERSION: 2.1 | DBSCHEMA: NOSCHEMA_DB | ORGANISM: Rhinopithecus roxellana | SPECIES: Rhinopithecus roxellana | CENTRALID: GID | Taxonomy ID: 61622 | Db type: OrgDb | Supporting
updated 9.2 years ago • zhangducsu
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 • Sturgill, David NIH/NIDDK [C]
power curve. I have a good number of samples (__85__), coming from 3 different organs, each at different developpement stages (5 replicates per stage). A mass spectrometry was performed, giving a spectral
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gt; #save in a TSV format (the file is saved in txt) >>> write.table(tmpgene,"Z:/**tomhait/organisms/human/** >>> transcript_names.txt", >>> row.names=FALSE, quote=FALSE) >>> #collect all sequences with upstream...as.character(transcript_**flank))) >>> >>> #writing to a ne…
updated 13.3 years ago • Stefan Kroeger
chr",c(1:19,"X","Y"),sep=""),2)) 2) rerun you command with the chr.map argument and a "custom" organism argument rnaSeq2 <- easyRNASeq(filesDirectory=extdataDir, organism="custom", chr.sizes=chr.sizes, filter=myfilt...validity.check=FALSE in the easyRNASeq command rnaSeq2 <- easyRNASeq(filesDirectory=extdataDir, …
am getting similar errors stating that there is no genome assembly fasta file available for these organisms. I tried with multiple versions of the AnnotationHub EnsDb object for each species and continue to get the same...snapshotDate(): 2022-10-31 Error in .local(x, ...) : No genome assembly fasta file available for organism: Xenopus tropicalis, data provider: Ensembl and genome version: Xeno…
updated 2.3 years ago • cjag
Code: > avn <- pathview(gene.data=pathview_genelist, pathway.id="avn01200", species = organism) > avn <- pathview(gene.data=gene_list, pathway.id="avn01200", species = organism, kegg.native = F) Error: > Note: Mapping
updated 2.7 years ago • morgan.sobol
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updated 10.6 years ago • mj
Ingelheim Foundation is recruiting a Post-Doctoral Fellow in Bioinformatics Proteome organization and dynamics (#AKPD02) The Institute of Molecular Biology (IMB) is a Centre of Excellence for Life Sciences located...Experience with mining and integration of large data sets with R and Python • Very good work organization skills and the ability to work independently • Work experience in…
updated 6.1 years ago • l.brown
I apologise if some version of this question has already been asked in some way- I could not find any issues that were similar to my own. I have a choice between taking data from the datasource package 'MotifDb' and 'JASPAR2018': MotifDb has a much larger wealth of data: <pre> library (MotifDb) library("BSgenome.Mmusculus.UCSC.mm9") tf_motif_hoco=subset(MotifDb, organism=='Mmusculus')…
updated 7.0 years ago • chrisclarkson100
gt; columns(org.Cs.eg.db) OrgDb object: | DBSCHEMAVERSION: 2.1 | DBSCHEMA: NOSCHEMA_DB | ORGANISM: Cannabis sativa | SPECIES: Cannabis sativa | CENTRALID: GID | Taxonomy ID: 3483 | Db type: OrgDb | Supporting package: AnnotationDbi
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had to add a pseudocount in order for it to run). The results were the following (I faceted them by organ to be "cleaner" to see any possible pattern in other subgroups): ![PCA Results][1] However, when performing DE in the full dataset
updated 2.8 years ago • andrebolerbarros
https://rdrr.io/cran/biomartr/man/getGFFSet.html library(biomartr) getGFFSet("refseq", organisms = c("Arabidopsis thaliana", "Arabidopsis lyrata", "Capsella rubella")) Running it online results in the following: Starting
updated 4.4 years ago • Matan G.
Hello, Bioconductor, I'm working lately with data from small-RNA seq in an organism without small RNA annotation. I would like to perform DE analysis on Differentially Expresed Regions and I would
updated 4.5 years ago • Konstantinos Yeles
the following: library(KEGGgraph) tmp &lt;- tempfile() retrieveKGML(pathwayid='mmu04015' , organism='mmu' , destfile=tmp, method="wget") pathway &lt;- parseKGML(tmp) nodes\[\[60\]\]@name\[\[1\]\] ---&gt; retrieves mmu:12801 nodes\[\[60\]\]@name\[\[1\]\] ---&gt; retrieves
updated 9.9 years ago • Osvaldo
<span style="font-size:13px; line-height:1.6">I am performing an analysis of targeted proteomics for a study with rather sophisticated study design. &nbsp;As a result of this and other issues (like novelty of the data itself) I found myself writing a lot of custom code &nbsp;(such as visualization, normalization, etc.). &nbsp;The code just begs to organize itself into a package.…
updated 10.9 years ago • petyuk
Hello everyone, I have a little bit confused in using biomaRt. I would like to retrieve GO term definition and name for each GO ID. I have done following mart &lt;- useMart(biomart = "ENSEMBL_MART_ENSEMBL", dataset = "hsapiens_gene_ensembl", host = "asia.ensembl.org") go_list &lt;- getBM(attributes=c("go_id", "name_1006", "namespace_1003"), filters = "…
updated 6.5 years ago • Taiki Tsutsui
up calculations I offer advice that they should download a copy of the KGML directory for their organism to their local machine, and I want the package to know where those files are at runtime. Thanks in advance, -Robert Robert
updated 15.2 years ago • Robert M. Flight
on R? Is there another easier way to load all the data at once? -&gt; What is the better way to organize the data to compare the samples coming from the patients infected with bacteria 1 and 2? Bacteria 1 20180202 LA 02
updated 6.8 years ago • pdaltron
Hi, I am attempting to do a differential expression analysis comparing one organism supplemented with bacteria and another that is not. When looking at my MA Plot it appears that there are man genes
updated 10.5 years ago • ejmcmaho
at the moment, but I use getBM in a loop over several marts because I need sequences of several organisms. Strangely, in the loop it works even fewer times. Currently I'm on host 'useast.ensembl.org', I've tried 'www.ensembl.org
updated 5.8 years ago • laurenz.holcik
<div class="preformatted">Hi , I'm a bit confused in the way of using my data. My input is a list of genes( in fact a list of targeted genes for microRNAs). The first step is to get the GoTerms associated to these genes and then i would like to do hyperg to obtain significant dysregulated Goterms. ALl the examples i went through use affy data or so so i'm not sure this is correct. I would …
updated 14.8 years ago • David
chrUn_gl000249 38502 countrabtex &lt;- easyRNASeq(filesDirectory=getwd(), + organism="Hsapiens", chr.sizes=chr.sizes, + readLength=58L, + annotationMethod="gtf", + annotationFile="merged.gtf", + count="exons...columns of result is not a multiple of vector length (arg 1) 2…
Hi, I'm trying to run create an annotation database for Agaricus bisporus through NCBI in AnnotationForge, but I get a couple of errors: Error in makeOrgDbFromDataFrames(data, tax\_id, genus, species, dbFileName,&nbsp; : &nbsp; 'goTable' GO Ids must be formatted like 'GO:XXXXXXX' In addition: Warning messages: 1: RSQLite::dbGetPreparedQuery() is deprecated, please switch to DBI…
new_pages/submission/sub_papers.html Workshops &amp; Tutorials: Submit a proposal to organize one! ---------------------------------------------------------------------- ---- The conference will begin with a day of workshops and tutorials: two full-day workshops and four half-day tutorials
updated 19.8 years ago • Hershel Safer
baseMapType = "ll",pkgName="Hum30kbatch1to5", pkgPath="C:/Installerade program/R/tempdir/hum", organism = "human", version = "1.1.0", makeXML = TRUE, author = list(author = "Johan Lindberg", maintainer = "johanl@biotech.kth.se"), fromWeb
updated 21.2 years ago • Johan Lindberg
is to identify mRNAs that are bound to one translational factor (compared to another factor) 2) Our organism has 8,000 genes 3) We use a modified RNAseq where each read represents one mRNA transcript. 4) and our library usually
data.frame(frame$go_id, frame$Evidence, frame$systematic_name) goFrame &lt;- GOFrame(goframeData, organism = "Saccharomyces cerevisiae") goAllFrame &lt;- GOAllFrame(goFrame) Sc.gsc &lt;- GeneSetCollection(goAllFrame, setType
updated 10.9 years ago • nonCodingGene
to a certain way of gene expression testing between sample groups) - Is available for a number of organisms and gene set annotations (at least GO and KEGG) - Allows one to ignore the direction of the regulation and concentrate
updated 14.7 years ago • Asta Laiho
to depend on other databases (e.g. miRbase) which are not very useful for more recently sequenced organisms where all we usually have is a fasta sequence file and a gff/gtf annotation file<span style="line-height:1.6">. Since
updated 10.7 years ago • Thomas Girke
RNAseq.course.html Booklet: http://www.bioinformatica.unito.it/RNAseq.pdf" Organizer: raffaele.calogero@unito.it -- ---------------------------------------- Prof. Raffaele A. Calogero Bioinformatics and Genomics Unit MBC Centro di Biotecnologie
updated 12.9 years ago • raffaele calogero
5 technical replicates (100 samples thus) The first two time points are really early is the organism's life cycle and hence we often expect less reads for some genes: After summing the reads from the technical replicates
updated 7.3 years ago • xei6
I am using the enricher function of clusterprofiler for GO enrichment of my non-model organism. First I have my DE genes (n=638, converted as character): gene &lt;- read.csv("list.csv", header = F,sep=",") gene &lt;- as.character
updated 5.7 years ago • tianshenbio
awk '($7 == "=")' &gt; output.sam, then it can run. ```r txdb&lt;-makeTxDbFromEnsembl(organism="Homo sapiens", release=103, circ_seqs=NULL, server="ensembldb.ensembl.org", username="anonymous", password=NULL, port
updated 4.7 years ago • stephen66
is.na(gc$entrezgene_id))] #entrez genes existant pour l'humain ens=gprofiler2::gconvert(genes, organism="hsapiens", target='ENTREZGENE_ACC')$target #entrez gene de nos genes ensint=factor(as.integer(ensfull %in% ens))#preparation
updated 5.4 years ago • emisecherre
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
Selected post-doctoral candidates will join a dynamic oncology drug discovery and development organization to study therapeutics that treats cancer. Candidates will have the opportunity to collaborate across the...Ingenuity) and internal sources in analyses. Candidates will work independently as part of a matrix organization. Candidates will communicate Bioinformatics results to computational bio…
updated 11.0 years ago • Michael Gormley
<div class="preformatted">After converting my custom gene2Domains mapping into a list of vectors &gt; head(entrez2interpro_nested) $`679594` [1] "IPR019956" "IPR019954" "IPR019955" "IPR000626" $`682397` [1] "IPR019956" "IPR019954" and feeding that into retrain(), I now have the 4th model (most complete?), built using genes: 5667 of 5667 features: 4007 level detectors: 78 This obsol…
genome as provided by NCBI (ASM33114v1, Jan. 2013) and stored in Biostrings objects. Version: 1.0 organism: Cicer arietinum species: Chickpea provider: NCBI provider\_version: ASM33114v1 release\_date: Jan. 2013 release...Shenzhen ASM33114v1 source\_url: https://www.ncbi.nlm.nih.gov/assembly/GCF\_000331145.1/\#/def organism\_biocview: Cicer\_arietinum BSgenomeObjname…
updated 8.5 years ago • jodiera
I would like to use `ggbio` for *C elegans* and am [following along with this tutorial for biovizBase][1]. When adding a **gene model track** the code looks like this: ``` library(ggbio) library(Homo.sapiens) #load gene symbol : GRanges, one gene/row data(genesymbol, package = "biovizBase") ``` Looking at the help for `?genesymbol` it looks like this is a dataset for humans. The pac…
updated 5.8 years ago • moldach
I used the latest database, but the data obtained than the old database, the lack of exactly what I want. As follows, I use the  "AnnotationHub(), query(hub,'zea') " function to get the results shown in the left, but I get the result is the right look, the lack of 'AH55736' is exactly what I want. ![](http://img.blog.csdn.net/20170811091923787) Then I try to change the "snapshotDate()" da…
updated 8.4 years ago • slbai01
I'm trying to use clusterProfiler to perform gene set enrichment analysis. My differentially-expressed gene dataset has Ensembl IDs in addition to log2foldChange values. First I ran the following chunk of code, and returned a "no term enriched under specific pvalueCutoff" error: ``` &gt; gse_hfd &lt;- gseGO(geneList = hfd_gene_list, ont = "ALL", keyType = "ENSEMBL", minGSSize = 3…
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updated 5.4 years ago • nico.komarowsky.ext
enrichResult (71.9 MB). If if look into it: &gt; edo # # over-representation test # #...@organism Homo sapiens #...@ontology DisGeNET #...@keytype ENTREZID #...@gene chr [1:1018] "49855" "9880" "8879" "11260" "1292" "55039" "3908" "85415" "10519
updated 4.2 years ago • Pahi
zmays_eg_gene dataset from genome annotation version of the plant_mart mart. biomartr::organismBM(organism = "zea mays") #We retrieve attributes from zmays_eg_gene for Zea mays zea_attributes &lt;- biomartr::organismAttributes
updated 23 months ago • sanchezsanchez
made a separate set that is just my intensities. In this case, we are looking at a mutant vs wt organism for differential protein expression. These both have 4 replicates. Once my data was filtered and I made a df (1014x18
updated 4.4 years ago • Chris
Hello,&nbsp; I have been trying to reproduce results from gsea&nbsp;using clusterprofiler and gseKEGG (for some unknow reason gseGO&nbsp;is not working for me ) simply repeating experiment on the same gene expression data about 13k genes:&nbsp; &nbsp;gseKEGG(geneList = zscores, &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &…
updated 8.0 years ago • Stane
use the bioconductor package goseq for go- term/pathway enrichment of my expression data. Since my organism of interest isn't included in the goseq database, I am manually entering the data for gene lengths and categories
updated 15.4 years ago • Joydeep Mitra
1,253 results • Page 11 of 21
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