Question: Tool problems when using older versions of downsampled tutorial data
1
gravatar for julieta
24 days ago by
julieta10
julieta10 wrote:

Hi, I'm a newbie in Ref-seq and I'm trying to make a pipeline using HiSat -> HtSeq -> DESeq2. I'm using the data that appears in https://usegalaxy.org/u/jeremy/p/galaxy-rna-seq-analysis-exercise The problem is that when executing DESeq2 it gives me this error and I do not know why. Please, can you help me? Thank you.

Fatal error: An undefined error occurred, please check your input carefully and contact your administrator. estimating size factors estimating dispersions gene-wise dispersion estimates mean-dispersion relationship -- note: fitType='parametric', but the dispersion trend was not well captured by the function: y = a/x + b, and a local regression fit was automatically substituted. specify fitType='local' or 'mean' to avoid this message next time. final dispersion estimates fitting model and testing Warning message: In checkForExperimentalReplicates(object, modelMatrix) : same number of samples and coefficients to fit, estimating dispersion by treating samples as replicates. please read the ?DESeq section on 'Experiments without replicates'. in summary: this analysis only potentially useful for data exploration, accurate differential expression analysis requires replication -- note: fitType='parametric', but the dispersion trend was not well captured by the function: y = a/x + b, and a local regression fit was automatically substituted. specify fitType='local' or 'mean' to avoid this message next time. Error in grid.Call(C_convert, x, as.integer(whatfrom), as.integer(whatto), : Viewport has zero dimension(s) Calls: generateGenericPlots ... makeContent.textrepeltree -> convertHeight -> convertUnit -> grid.Call Warning message: In sparseTest(counts(object, normalized = TRUE), 0.9, 100, 0.1) : the rlog assumes that data is close to a negative binomial distribution, an assumption which is sometimes not compatible with datasets where many genes have many zero counts despite a few very large counts. In this data, for 20% of genes with a sum of normalized counts above 100, it was the case that a single sample's normalized count made up more than 90% of the sum over all samples. the threshold for this warning is 10% of genes. See plotSparsity(dds) for a visualization of this. We recommend instead using the varianceStabilizingTransformation or shifted log (see vignette).

diffbind dexseq deseq2 rna-seq • 85 views
ADD COMMENTlink modified 23 days ago by Jennifer Hillman Jackson25k • written 24 days ago by julieta10
0
gravatar for Jennifer Hillman Jackson
23 days ago by
United States
Jennifer Hillman Jackson25k wrote:

Hello,

The data in that older tutorial is a subset of larger datasets. It was designed to be as small as possible yet still be functional with the older tools, to demonstrate usage of which many are now deprecated: Tophat, all Cuff* tools. The content is too sparse to use with the newer tools and is not representative of a full-size experiment.

Instead, try using the tutorial data below to learn how to use these updated tools. It has more complex content designed in a way that doesn't require special parameter handling for the subsetted content.

Galaxy tutorials: https://galaxyproject.org/learn/ - RNA-seq: Discovering and quantifying new transcripts - an in-depth transcriptome analysis example. https://galaxyproject.org/tutorials/nt_rnaseq

Thanks! Jen, Galaxy team

ADD COMMENTlink written 23 days ago by Jennifer Hillman Jackson25k
Please log in to add an answer.

Help
Access

Use of this site constitutes acceptance of our User Agreement and Privacy Policy.
Powered by Biostar version 16.09
Traffic: 178 users visited in the last hour