713 results • Page 5 of 12
When I set the contrast in DiffBind as ``` # Contrast from normalized object dbObj_contrast_manual <- dba.contrast(dbObj_norm, design="~Condition") dbObj_contrast_cells
updated 11 months ago • Sam
Hello, I am analyzing some ChIP-seq data with Diffbind, and everything works great until when I was trying to use its plotprofile funtion. The command and error messages
updated 3.3 years ago • zhuyi05
I have a very simple question regarding the dba.plotProfile function in Diffbind. I couldn't find an answer online, but would appreciate someone linking the answer, if it already exists somewhere
updated 3 months ago • Tara
do not get any significant peaks by MACS, so the output peaks file is empty. When I use that file in DiffBind sample sheet, I get an error: <pre> Error in read.table(fn, blank.lines.skip = T, header = T) : no lines available in input Calls
updated 8.4 years ago • igor
div class="preformatted">Dear Dr. Brown, I asked the questions earlier regarding the DiffBind last week. I have versioned up to R3.0.1 and Bioconductor 2.12, and I checked to see how DiffBind 1.6.2 works. But the...chiba-u.jp=""> &gt; &gt;To: <bioconductor at="" r-project.org=""> &gt; &gt;Subject: [BioC] About the DiffBind dba.count() crash problems &gt; &gt;…
updated 11.5 years ago • kentanaka@chiba-u.jp
Love the new design feature of DiffBind! However, I am having trouble writing the contrast for the interaction terms. I've used this [tutorial][1] for writing...contrasts in DESeq2 for RNA seq results and thought the approach would work in DiffBind. ```r DBA &lt;- dba.contrast(DBA, design = '~ Condition * Treatment') DBA$DESeq2 $names [1] "Intercept" "Condition_MUT_vs_…
updated 3.6 years ago • lindsaynhayes
don't know whether the difference is due to real biology, or due to some technical problem. I used DiffBind for detecting differential H3K27Ac. As expected I get much more peaks which are up at the disease tissue. Are there...any suggestions for what would be the best normalization in DiffBind in such a case, or how can I try understanding whether this is an artifact? Thank you
updated 4.1 years ago • GFM
Hello, I tried to do test run of Diffbind for my ChIP-seq data. I followed the manual and used the basic command. these are my command :&nbsp; &nbsp; l<span style="background...color:Yellow">ibrary(DiffBind) setwd("/project/maheshid/mforoo1/DiffBind") samples &lt;- read.csv("H3K4me3.csv", header=TRUE) names(samples) samples</span
updated 7.5 years ago • mforoo1
Hi all, So am using the diffbind R package and I was doing some plots after analyzing my samples. using the dba.plotVolcano and the option &gt; bLabels
updated 5.3 years ago • theodore.georgomanolis
cruk.cam.ac.uk<mailto:rory.stark@cruk.cam.ac.uk>&gt; Subject: Have I extracted the right data with DiffBind? Dear Stark, I have 17 peaksets wiht four examples in the mail attachments. I want to extract ranges shared by at least...4 of the 17 peaksets. And then I run the following code under "DiffBind" package: &gt;bedfilelist2=dba(sampleSheet="bedfilelist2.csv",attributes=DBA_ID,c…
updated 10.7 years ago • Rory Stark
Dear Rory &nbsp; First I wan to thank you for making Diffbind an easy access tool. I have been using it a lot and I have a couple of questions. &nbsp; I have been looking for a description
updated 9.9 years ago • medinaale
Hi, I'm having issue with dba.contrast() in DiffBind v3.4.0. I have two conditions, and each condition has 3 replicates. I'm working a simple differential peak analysis
updated 3.0 years ago • AMA
are from different tissues, no replicate. I want to differentiate them according to 5 conditions by DiffBind package, and display result on heatmap. So I did as follows: &gt;ALL &lt;-&nbsp;dba(sampleSheet="mysamples.csv") &gt;ALL\_count
updated 6.3 years ago • mengm5
the problem and the peaksets are read in. The question is if the peak scores are considered by DiffBind at all, and if the problem that arises later on (no way to get beyond __factorname = dba.analyze(factorname) __is a result
updated 9.6 years ago • iliya.lefterov
theresas@usc.edu] Sent: 15 February 2014 02:01 To: Rory Stark; Gordon Brown Subject: minOverlap in DiffBind in R- what does it mean? Greetings Drs, Stark and Brown, my name is Theresa. I have just started using DiffBind and can't...package. I have gone through your tamoxifen tutorial and have read through forums and threads on DiffBind online. but I still can't ferret out what "minOverlaps=…
updated 10.8 years ago • Rory Stark
wherein I am given a few BED and BAM files to analyse and see how similar they are. I am using the diffbind package to do so. The first correlation map(heat map), when I run &gt;&gt;&gt;MB &lt;- dba(sampleSheet="MBdataframe.csv")&nbsp
updated 8.4 years ago • shubhibartaria
Hello! I have a really basic question! In the `DiffBind` vignette, I have a question regarding the following texts: &gt; If bFullLibrarySize is set to TRUE (default), then sizeFactors...sample, divided by the minimum of these; otherwise, estimateSizeFactors is invoked. How does `DiffBind` internally calculates the number of reads of a BAM file to make those *sizeFactors*? In par…
updated 4.5 years ago • bioinfouser2
Hello everyone, I have a simple question; I am doing a DiffBind analysis and using dba.contrast function what's the difference if we do in diffBind contrast ie: WT vs Control and
updated 6 months ago • zzrammal
the body of text here Code should be placed in three backticks as shown below ```library(DiffBind) getwd() setwd("/Users/tsompana/Box/6. PROJECTS/8. Justin.Fasting.Enzalutamide.ATAC-seq/3.DiffBind/3.DiffBind_csv_files...csv file samples = read.csv("Screening.csv", header=TRUE, sep=",") #read peaksets using the "dba" DiffBind function screening = dba(sampleSheet = "Screening.csv") s…
updated 3.3 years ago • mtsompana
Hi, DiffBind (v3.4.11) dba.analyze function doesn't have bSubControl option anymore? dba.analyze function (bGreylist=FALSE
updated 14 months ago • r.murakami
Hi, Using DESEQ2 and EDGER in diffBind gives huge difference in total number of differentially bound sites around 8000 for DESEQ2 and around 700 for...Hi, Using DESEQ2 and EDGER in diffBind gives huge difference in total number of differentially bound sites around 8000 for DESEQ2 and around 700 for EDGER
updated 5.3 years ago • dewshrs
Hi all, I am trying to find which genes are different in chromatin accessibility so I used nf-core/ATAC pipeline then feed the bam files and broadpeak files output into Diffbind. I got around 100k peaks, 21k genes after annotated peaks by ChIPpeakanno, and after sorting the top genes by Fold. I...so I used nf-core/ATAC pipeline then feed the bam files and broadpeak files output into Diffbind. I g…
updated 18 months ago • Chris
When I used dba.cout with DiffBind, the following error occurred. Code should be placed in three backticks as shown below ```r library(DiffBind) library
updated 2.9 years ago • tjhwangxiong
nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; I am trying to analyze ChIP-Seq data using DiffBind. After creating a CSV file with the experiment design and the peak files information. like shown in the DiffBind vignette...utils&nbsp;&nbsp;&nbsp;&nbsp; datasets&nbsp; methods \[8\] base other attached packages: \[1\] DiffBind\_1.8.5…
updated 9.7 years ago • surjray
Hi, I'm using DiffBind for many of my ChIPseq analyses and recently asked myself, if the "concentration" that is given as output of dba.report
updated 3.7 years ago • roman.hillje
Hi,&nbsp; I got an error when I used DiffBind to treat a human ATAC-seq library data set. (see &nbsp;https://support.bioconductor.org/p/94915/).ATAC-seq is the data...Hi,&nbsp; I got an error when I used DiffBind to treat a human ATAC-seq library data set. (see &nbsp;https://support.bioconductor.org/p/94915/).ATAC-seq is the data set
updated 7.6 years ago • zhaolin20042008
I would do this if A) is the right answer. However, if it is B) then IDR is somewhat redundant, as diffbind would just tell me all of the peaks that are significant.&nbsp; Thanks in advance. -Wes
updated 8.0 years ago • wesley.cai
<div class="preformatted">Hi Marta- Well spotted! I have been able to reproduce the behavior you describe, and found the cause. edgeR tends to report normalized counts-per-million (cpm), which is good for comparing counts between experiments but uses values that are potentially on a much different scale than for the original experiment. Instead of scaling every experiment to one million r…
Hi! DiffBind is great stuff! I am trying to do a DiffBind analysis comparing 6 conditions (CT00, CT04, CT08, CT12, CT16, CT20). I have managed...output only reported Conc\_CT00 and Conc\_CT04. So, what do the 21 contrast mean? Should I do one DiffBind analysis for each pairwise comparison (CT00-CT04, CT00-CT08, CT00-CT12...CT16-CT20)? &nbsp
updated 8.7 years ago • j.m.fustin27
My output files from the Genrich are .log and .narroPeak files. Can I use the peak files in DiffBind? Thanks! Gayani
updated 5.7 years ago • gsenevirathne
Hi, I'm confused by how DiffBind uses the spike-ins for normalization. My understanding of the manual is that DiffBind calculates the spike-in reads
updated 21 months ago • Weisheng
normalised read counts should be used. You can work with RPKM values for the plotting features of DiffBind (by setting score=DBA_SCORE_PRKM in the plotting function, or in dba.count, where the score can be reset at will if...aur?lie teissandier" <aurelie.teissandier at="" curie.fr=""> wrote: &gt;Dear Rory, &gt; &gt;I use diffbind with Deseq. And I look in the newCountDataSet ob…
updated 10.9 years ago • Rory Stark
such that one can look at the plot and see the density along the length of the chromosome. From the diffbind table, what column can I use to plot the read density? Can I use the Fold column? Thank you so much for any help or guidance
updated 20 months ago • bhandary.8590
Hi Everyone I have ChIP-Seq in a strain with defined maternal/paternal background and Now I want to use DiffBind to perform allele-specifc binding analysis. But what should be the design of analysis in this case? I can think of different...I have ChIP-Seq in a strain with defined maternal/paternal background and Now I want to use DiffBind to perform allele-specifc binding analysis. But what shou…
updated 9.6 years ago • Vivek.b
I retrieve DiffBind results as a DESeq2 object, and then look how many differentially bound regions are within it. When doing this, I get...a different number of DB regions compared to the original DiffBind object. ```r library(DESeq2) library(DiffBind) data(tamoxifen_counts) tamoxifen &lt;- dba.contrast(tamoxifen, design
updated 3.7 years ago • Sam
normalization was set to spike-in. I'm now planning to conduct differential analysis with DiffBind and have included the spike-in BAM files in my sample sheet. Could someone please advise on the appropriate parameters
updated 25 days ago • kim
div class="preformatted">Dear Rory, I finally analyze my data with DiffBind and it seems working well, I was wondering whether is possible or it will be possible in the next release to export
updated 12.2 years ago • Paolo Kunderfranco
Hi, I am getting the following errors while using DiffBind to output the peakset . dba(data, bSummarizedExperiment=TRUE) Error in FUN(X\[\[i\]\], ...) : &nbsp; assay rownames() must be NULL or equal
updated 8.2 years ago • svohra
differential peak finding, drawing Venn diagram and PCA plot) my m6A-seq data recently using DiffBind. However, as the program is developed originally for analyzing ChIP-seq data, I'm hesitant to apply default settings...events will make aligner generate large gaps between alignments. So maybe some parameters of DiffBind should also be tweaked manually. I'm wondering which parameter should I part…
updated 21 months ago • zhiyi
I am learning the DiffBind package, and I have some questions not covered by the vignette. 1) Is the peak score relevant to **affinity** analysis...I am learning the DiffBind package, and I have some questions not covered by the vignette. 1) Is the peak score relevant to **affinity** analysis, and
updated 3.7 years ago • Sam
each factor might have different frip, and it can cause biases in the comparisons. Is it OK to use DiffBind / csaw to compare these two ChIP seq samples (with replicates of course)? Thanks
updated 4.4 years ago • GFM
I've been trying to use DiffBind for ATAC-seq data. I noticed that there is a large difference in differential accessibility depending on whether
updated 5.8 years ago • paz2005
nbsp; I have questions about "dba.report", I applied "DiffBind" to analyze my dataset like: &nbsp; <pre> H3K27ac_CellA_CellD &lt;- dba(sampleSheet="sampleconfiguration.csv",) H3K27ac_CellA_CellD_Count
updated 7.5 years ago • JunLVI
Hello, I am quite comfused about the mechanism and detailed process of background normalization in diffbind normalization. As the manual depicted, "The core background normalization technique is to divide the genome into
updated 7 weeks ago • Young Boqin
two things: the first is to override the column choice given above, so that I can for instance force DiffBind to use signalValue column; the second is to indicate normalization is TRUE/FALSE. Thank you Teck Por Lim National
updated 9.6 years ago • teckpor
Hi, I'm trying to understand the normalization for DESeq2 analysis within DiffBind. &nbsp;If I run: <code>Pool1 = dba.analyze(Pool1,method=DBA_DESEQ2,<strong>bFullLibrarySize=FALSE</strong>,bCorPlot...Hi, I'm trying to understand the normalization for DESeq2 analysis within DiffBind. &nbsp;If I run: <code>Pool1 = dba.analyze(Pool1,method=DBA_DESEQ2,<strong&g…
updated 9.5 years ago • JasonLouisStein
Hi, We use DiffBind for the differential binding analysis of our ChIP data. In this we use edgeR TMM for normalization. I would like to...really appreciated. Thank you. ``` indiff &lt;- dba(sampleSheet="//smb.cluster/080719ATACseq/Diffbind/SampleSheets/AAG57_0v2_SampleSheet_desktop.csv") indiff indiff_count &lt;- dba.count(indiff, minOverlap=2) indiff_count...norm$lib.sizes/n…
updated 3.5 years ago • Nico
Hello,&nbsp; <span style="line-height:1.6">I am trying to use diffbind on paired end read data. I have done the following to get our proper peaks of interest ( we have technical replicates
updated 9.1 years ago • jess.schust
Dear all, I am using DiffBind for ChIP-Seq and CUTnTag analysis and would like to switch off subtracting reads of control samples. For this, I set...bSubControl=FALSE` in `dba.count()`. However, DiffBind results are exactly identical no matter if I set bSubControl to TRUE or FALSE. I tried this for several R and DiffBind
updated 10 months ago • frueher
But I don't want to get a consensus peak set. So I add "peaks=NULL" according to the document of DiffBind. Here is my code: ``` &gt; data$config$singleEnd &lt;- F &gt; data &lt;- dba.count(data,peaks=NULL,bUseSummarizeOverlaps=T) Error
updated 5.1 years ago • shen_
Hello I am using DiffBind for ATAC-Seq analysis. I would like to remove peaks located on random chromosomes and chrUn (Unplace Chromosome...Hello I am using DiffBind for ATAC-Seq analysis. I would like to remove peaks located on random chromosomes and chrUn (Unplace Chromosome). I
updated 3 months ago • mdidish
0, 0)">i fferential&nbsp;binding&nbsp;analysis&nbsp;of&nbsp;ChIP-Seq&nbsp;peak&nbsp;data </span>with DiffBind<span style="background-color:rgba(0, 0, 0, 0)">. I´m trying to use the code explained in the post: </span>https://support.bioconductor.org...peaksets between TFa and TFb. Here I paste the output from the console: &nbsp; &gt; library(…
updated 8.7 years ago • jvdelarosa
Hello, I'm new to DiffBind and have 3 tissues with 2 replicates each. I have been able to generate plots with contrast 1-3 to compare each pair
updated 4.0 years ago • Divya
I'm trying to prevent Diffbind from merging overlapping peaks in my bed file (TSS file with exactly 2000 bp widths) by setting DBA$config$mergeOverlap
updated 22 months ago • slrpatty
Hi everyone, im trying to install Diffbind to identify unique enriched peaks from treatment and control data. i cant able to install diffbind in R it shows error...status 28: In install.packages(pkgs = doing, lib = lib, ...) : &nbsp; installation of package ‘DiffBind’ had non-zero exit status &nbsp; &nbsp
updated 8.2 years ago • gskbioinfo143
I am a little puzzled by the way of generating a dba report from DiffBind matrix. When I run dba.report(mat, contrast=1), this should run with default fold and p-values, which should be 1 (fold...I am a little puzzled by the way of generating a dba report from DiffBind matrix. When I run dba.report(mat, contrast=1), this should run with default fold and p-values, which should be 1 (fold) and
updated 5 weeks ago • aelbassiouny
This is a question on the "summit" function in DiffBind. I would like to generate a set of consensus peaks with width of 201bp, centered around the peak summit. The codes I...This is a question on the "summit" function in DiffBind. I would like to generate a set of consensus peaks with width of 201bp, centered around the peak summit. The codes I used...retrieved from here:&nbsp;https://www.…
updated 7.0 years ago • meisan406
Hi, I want to use DiffBind for differential accessible chromatin regions for my ATACSeq analysis. I am trying to understand the core codes...for this analysis as described in DiffBind manual but getting bit confused due to many interlinked options. If the metadata (information of case, control, replicates...with the command "dba.analyze("File.csv")". With this scenario I have three questions: …
updated 20 months ago • tahir.msajid
Dear Rory, I am currently using DiffBind to detect differential chromatin accessibility using ATAC-seq data. We are testing a few different ways of doing
updated 8.1 years ago • julien.bryois
of these, are also possible." Is there guidance somewhere to do this? How can this be done with Diffbind? Thank you, Ian
updated 7 months ago • Ian D.
713 results • Page 5 of 12
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