1,735 results • Page 7 of 29
in which I can find the theory (included formulas and proof) beyond this approach. I read a lots of papers about this argument but in some cases they don't help me to clarify my doubts. I thank you in advance
updated 8.5 years ago • erika_lilly
www.ebi.ac.uk/goldman-srv/rlsim/. But the latest version of rlsim is 2014. And the corresponding paper seems to be a BioRxiv article from 2015... which seemingly has never been published. Thank you in advance. RM
updated 6.5 years ago • Ramiro Magno
trying to estimate the variability technical replicates from different microarray platforms. The few papers I found on this topic and current opinion seems to suggest that technical replicates are not required for microarrays
updated 17.7 years ago • Adaikalavan Ramasamy
It looks like DESeq2 has been used efficaciously for MS data in published papers (<https://www.ncbi.nlm.nih.gov/pubmed/?term=26193490>). &nbsp;However, that is for unlabeled MS data, in which the only information
updated 8.5 years ago • maduanduan8
method is used for specific data type, such as steady-state or time course. Is there a evaluation paper on this topic? Best, Pengcheng
updated 8.9 years ago • Pengcheng Yang
it into a flowFrame, so far I've just being able to do this (by following the instructions from a paper from BD): set.sub &lt;- fsApply(fs, function(x) {samp &lt;- sample(1:10000, size = 100) set.sub&lt;-new('flowFrame',exprs = x\[samp,\])}, use.exprs
updated 9.4 years ago • cherryzt
The paper "Oldham, M.C., P. Langfelder and S. Horvath, Network methods for describing sample relationships in genomic datasets: application
updated 7.3 years ago • 2323982403
Learning and Applications (ICMLA 2009)" to be held in Miami, Florida, USA, 13-15 Dec. 2009. The paper submission seadline is: July 15, 2009. More details at: http://www.icmla-conference.org/icmla09/CFP_SpecialSession8.html
updated 16.5 years ago • Tarca, Adi
<span style="line-height:1.6">Hi,</span> Somatic signatures package uses RSS and unexplained variance to assess the best number of signatures. In Alexandrov et al paper (Cell Reports 3, 246-259) they used cosine similarity and Frobenius reconstruction error to determine the number of signatures...uses RSS and unexplained variance to assess the best number of signatures. In Alexandrov…
updated 10.3 years ago • Asma rabe
https://rnbeads.org/data/install.R') Bioconductor version 3.14 (BiocManager 1.30.16), R 4.1.0 (2021-05-18) Installing package(s) 'RnBeads' also installing the dependencies ‘gsl’, ‘genefilter’, ‘GSEABase’, ‘lumi’, ‘aws’, ‘IlluminaHumanMethylationEPICanno.ilm10b4.hg19
updated 3.8 years ago • nabiyogesh
c("RRM2", "BIRC5", "TOP2A")) : DGIdb service not available. sessionInfo( ) R version 4.1.2 (2021-11-01) Platform: x86_64-pc-linux-gnu (64-bit) Running under: Ubuntu 20.04.3 LTS Matrix products: default BLAS: /usr/lib/x86_64
updated 3.9 years ago • DannyM
a1) : could not find function "colMax" ?colMax sessionInfo() R Under development (unstable) (2021-01-28 r79891) Platform: x86_64-apple-darwin17.0 (64-bit) Running under: macOS Mojave 10.14.6 Matrix products: default BLAS
updated 4.6 years ago • Habil Zare
Hello, I'm reading the DESeq2 paper, and i have two questions regarding the prior for LFC. 1) For the variance of the normal prior for LFC, I am wondering why...Hello, I'm reading the DESeq2 paper, and i have two questions regarding the prior for LFC. 1) For the variance of the normal prior for LFC, I am wondering why the
updated 6 months ago • Chenghao
counts in CPM. **But what is the actual normalization method used?** I am going along using this [paper][1]... so is it normalisation by distribution it uses or by library size? Any help to understand this is highly appreciated
updated 4.2 years ago • Caroline
the results of my pipeline with previously published experiments but I dont seem to find any papers using the current version of DESeq2 (v1.30.0) with available reads. I found that installing previous versions of DESeq2
updated 4.9 years ago • Samuel Daniel
<div class="preformatted"> Friends, Could you, please, help me to find gene expression meta analysis tutorial. I have several microarray studies and need to combine them. I am not bioinformatician/biologist, so I need really step-by-step instructions. Sometimes, authors supply their papers with step-by-step instructions. I need something that will work, and I don't carry about quality of r…
updated 11.6 years ago • Guest User
Hello, I'm trying to use EBseq-HMM to analyze some time course data. In my case I have 12 time points with 3 biological replicates, 36 samples in total. When I run the pipeline, it seems that it needs an lot of resources, running it in a cluster asking for 64gb of ram does't seem to be enough to finish de analysis. The resources needed to run this pipeline are not discussed in the paper and I ju…
updated 9.8 years ago • liamarseg
Hi Michael, I've read you paper on DESeq2 (Moderated estimation of fold change and dispersion for RNA-seq data with DESeq2) and have a question about
updated 9.7 years ago • ilyaal
Hi, I am using DRIMSeq / DEXSeq-DTU workflow describe by Love at al. 2018. According to the paper, 'scaledTPM' option is chosen for normalisation (latter on 'dtuScaledTPM' option was added to the tximport package). 1) What
updated 5.5 years ago • aleksandar.baburski.g
ST 1.0 array, I have been tried to search existed packages for process this kind of data. There is a paper "Comprehensive Analysis of Affymetrix Exon Arrays Using BioConductor" descried the package 'exonmap' seems no longer
updated 11.7 years ago • Guest User
Hi, I have followed [this](https://f1000research.com/articles/5-1438/v2) paper but I have problem to undestand the following piece of code: &gt; pch &lt;- c(0,1,2,15,16,17) &gt; colors &lt;- rep(c("darkgreen", "red", "blue
updated 8.2 years ago • mictadlo
find for the microorganism I am working with i.e. *Clostridium beijerinckii* NCIMB 8052. I have read paper and information about it that it is a number to identify genes specifically but I am struggling with finding the source
updated 6.2 years ago • mnazir
div class="preformatted">some have asked me about a reference for gcrma... a paper is now officially accpeted by the journal of the american statistical association (JASA). you can get the info here: http
updated 21.4 years ago • Rafael A. Irizarry
itself. e.g. SP1 gene is interactiong with itself or have a loop or activating. i need reference paper or tool or website link just to use for reference. Please guide me ASAP. if anybody is interested but dn't want to give &nbsp
updated 9.0 years ago • shaheryar
how did you calculate the "baseMean counts" in the output of DESeq2. I looked the Genome Biology paper and additional files, it seems you used mean counts or mean expression there. If you give the "baseMean counts" as an output
updated 10.0 years ago • zpingfeng
or "KO~"WT". I tried both way, the results are quite different. The way described in the original paper on how GSEA works does not seem give an excuse how this parameter affect the results, and why this happened. Please help
updated 13.7 years ago • wenhuo hu
fold-change is greater than 1.5 (on a log2 scale). For the estimated fold change, does the paper mean that avg_logFC &gt; 1.5 or FC &gt; 1.5 and avg_logFC &gt; 0.58 (knowing that log2(1.5) = 0.58)? Also, it is not clear to me how the
updated 6.0 years ago • ahmed.abbas
div class="preformatted">Hi, All: As part of the suggestions from a reviewer of my submitted paper, I am asked to provide the IM (Ideal Mismatch) values generated from MAS5 for some probes of some probeset. I know BioConductor
updated 18.8 years ago • Wang, Yonghong NIH/NCI
oligonucleotide array probe level data. Biostatistics. 2003 Apr;4(2):249-64. and a number of other papers by the same first author. David Rocke and Blythe Durbin have a number of papers, as far as I know they, as well as Trey Ideker
<div class="preformatted">Dear Bioconductors, In evaluating several RNA-seq analysis techniques, I decided to analyse the same SEQC spiked-in dataset as mentioned in the limma-Voom paper (Law et al. 2014, Genome Biology). This dataset contains 92 genes, 69 of which are spiked-in at different concentrations. As in the paper, I copied the 23 non DE genes twice, providing me a dataset with a …
updated 11.8 years ago • Koen Van den Berge
to integrate using MNN_correct and then perform DE, reproducing the method presented in the [MNN paper][1]. I would appreciate your opinion on my rationale. I have processed both datasets and then corrected using mnn_correct...variable (GSE1, GSE2) X the feeding condition variable (Fed, FD). [Reproducing the logic of the paper][2]. My aim is to get the effect of food deprivation for this cell …
Hi, I'm attempting to download the datasets that go with the paper ["Clinical utility of microarray-based gene expression profiling in the diagnosis and subclassification of leukemia...with the R package GEOQuery. There are two datasets (stage 1 and 2) associated with the research paper, and the and I've been using these commands to download them both: <pre> <strong>&gt;librar…
updated 8.4 years ago • mmayo
<div class="preformatted">Dear limma experts, I am analyzing the data set given to me and described by these the column names of my MA object: &gt; colnames(MA.hyp) [1] "../ampcon/mev/C0-_1stround_vs_C60-_1stround_13263536.mev" [2] "../ampcon/mev/C0-_2ndround_vs_C60-_2ndround_13263534.mev" [3] "../ampcon/mev/C60-_1stround_vs_C0-_1stround_13263533.mev" [4] "../ampcon/mev/C60-_2ndround_…
updated 19.4 years ago • Andrew Mcdonagh
of replicates and samples are less than or equal to 5. We upgraded the LPE package from the original paper (2003), and published a paper in BMC Bioinformatics. The latest version is on Bioconductor since early last year. (http://www.biomedcentral.com...question: How can one run simply the Bonferroni adjusted LPE test from your 2003 Bioinformatics paper (Figure 2 and page 1948), using the LPE R p…
updated 19.8 years ago • Jain, Nitin
the form at [https://forms.gle/bSRaA2btAEsYDiCN9][2]. Applications close on Friday 26th February 2021. Questions about the role can be directed to current board members (contact details can be found at [https://bioconductor.org
updated 4.8 years ago • Matthew Ritchie
indicating differences in the distributions? On the one hand, the smooth quantile normalization paper seems to imply this. On the other hand in previous posts Gordon Smyth has stated that TMM is usually the best way to proceed
examples of people filtering out immunoglobulin genes during RNA-seq analysis, such as in this paper : https://www.nature.com/articles/s41467-019-11373-9 However, I am interested in the immunology of the condition I am studying
updated 4.3 years ago • maria.papanikolaou
I'd like to get a precise and intuitive understanding of how empirical Bayes moderation (conducted by `eBayes` function of the `limma` package) in the `limma` analysis pipeline works. I tried to read through the [original paper](https://www.degruyter.com/document/doi/10.2202/1544-6115.1027/html) but found it too technical and time-consuming. Could...the `limma` package) in the `limma` analysis pi…
updated 4.5 years ago • Junghoon
have been prepared with the small sample target protocol for the human plus2.0 chip I remember of a paper by Irizzary on a modified RMA for small samples. Can someone give a suggestion on the analyse to run, better the classical
updated 18.0 years ago • marco fabbri
div class="preformatted">Hi I was just browsing through my collection of papers and came across this one: http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&amp;db=pubmed&amp;d op t=Abstract
updated 21.3 years ago • michael watson IAH-C
Dear all, I have found this paper: [piRNAs Are Associated with Diverse Transgenerational Effects on Gene and Transposon Expression in a Hybrid Dysgenic
updated 9.5 years ago • ribioinfo
outliers in these part of the spectrum but what else if they are excluded from analysis ? Is there a paper / study which deals with the distribution of gene expression for extreme values that somebody can suggest me ? thanks
updated 21.2 years ago • Phguardiol@aol.com
to use loess normalization function based on externals controls (like MSP) as in Yang et al.; 2002 paper. I work with bioconductor marrayNorm package. I identified my controls in the maControls structure of marrayLayout
updated 21.6 years ago • Ghislaine Guigon
Hi Julie, I have read a paper titled "Genome-scale measurement of off-target activity using Cas9 toxicity in high-throughput screens",and have found
updated 6.1 years ago • XIN1988
values of log2folchange were lower than 1 (the MA plot is attached). Now I started to write my paper and I saw that several authors used log2foldchange &gt; 1 as cutoff to downstream analysis as functional analysis. Do
updated 11.1 years ago • acesar
for security reasons. Does anyone have a copy of Bioconductor on CD-ROM they can send me by paper mail (p-mail), and then could I load the code from the CD-ROM into R? (Presumably I'd need to script to load into R?) Thank you for
updated 20.1 years ago • jro203
can get a pretty good idea of how to proceed by working through the supplementary material of the paper, it has it's own repos at: Also Sophie there is a github thread for phyloseq with deseq at: http://joey711.github.io/waste
updated 11.7 years ago • Susan Holmes
<div class="preformatted">Hello all, I know this has probably been asked several times, but would anybody know of a little textual description of how RMA works? I am very familiar with the papers on the issue, but would anybody know of a simplified text that one could use to explain the method to people that are not...but would anybody know of a little textual description of how RMA works? …
updated 21.2 years ago • Lawrence Paul Petalidis
in edger one gets lots of values &lt;1. Unfortunately, I found neither in edger manual nor in edger paper the description how the log fold change is calculated. Especially how those values &lt;1 are treated because for instance
updated 9.9 years ago • tonja.r
div class="preformatted">hi, A few papers have concluded that DESeq is more accurate for DE genes discovery than methods using FPKM, and that the bias in FPKM
updated 12.4 years ago • Jike Cui
div class="preformatted">Dear All, Recently I found an interesting paper about problems with RMA when applied to small sample sets which are based on the median-polish algorithm, see: http://www.biomedcentral.com
updated 15.0 years ago • cstrato
An embedded and charset-unspecified text was scrubbed... Name: not available Url: https://stat.ethz.ch/pipermail/bioconductor/attachments/20071019/ 9166f717/attachment.pl
updated 18.2 years ago • Ana Conesa
<div class="preformatted">In the paper: Exploration, Normalization and Summaries of High Density Oligonucleotide Array Probe Level Data the following statement...div class="preformatted">In the paper: Exploration, Normalization and Summaries of High Density Oligonucleotide Array Probe Level Data the following...be "before gcrma". This explanation made sense to me, but seems to contradic…
updated 19.5 years ago • noel0925@sbcglobal.net
height:355px; width:1038px"/> I did look at the vignette, the documentation, the sashimi plot paper https://academic.oup.com/bioinformatics/article-abstract/31/14/2400/254271/Quantitative-visualization-of-alternative...s when I realized the meaning of the Y-axis label (which is not part of the original sashimi plot paper). So, I just want to make sure that we got the interpretation correctly…
updated 9.0 years ago • Leonardo Collado Torres
<div class="preformatted">Dear limma experts I am analyzing the data set given to me and described by these the column names of my MA object: &gt; colnames(MA.hyp) [1] "../ampcon/mev/C0-_1stround_vs_C60-_1stround_13263536.mev" [2] "../ampcon/mev/C0-_2ndround_vs_C60-_2ndround_13263534.mev" [3] "../ampcon/mev/C60-_1stround_vs_C0-_1stround_13263533.mev" [4] "../ampcon/mev/C60-_2ndround_…
updated 19.4 years ago • Andrew Mcdonagh
div class="preformatted">Hi, is there any paper or explanation of how should I interpret heatmap with dendrogram. symbs &lt;- getSYMBOL(myFeatureGenes,"moe430a"); symbs
updated 21.2 years ago • SAURIN
significance of a result assuming some prior rate of false discovery (type 1 error). I read the 1995 paper for the BH method but I am still confused on what exactly determines this rate? Is it done in a parametric way or non-paramterically
updated 12.4 years ago • Cornish, Joseph NIH/NIAID [F]
isoform level information (situation similar to that shown in Figure 1C of the Sonenson et al paper on the tximport package). I am trying to find the best set of parameters for DE analysis.&nbsp;Is it better to use the transcript
updated 8.5 years ago • sunil.mangalam
from the community. I have searched the internet but found just a couple of discussions and papers about selecting control genes (i.e. housekeeping) for real time pcr verification of microarrays results, but nothing
updated 19.6 years ago • Mike Ferker
from origins. From reading the vignette this application seems fine, but after reading the original paper we weren't so sure. Thank you, Adam Cornwell [[alternative HTML version deleted]] </div
updated 12.9 years ago • Cornwell, Adam
1,735 results • Page 7 of 29
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