Unconfigured Ad
Collapse
X
-
The tuxedo procotol article has a section on what you want: http://www.nature.com/nprot/journal/...tml#/procedure check steps 16-18, there is some simple R code that you could follow and expand.
-
This is helpful. Thank you!Originally posted by ETHANol View PostThere should be a file gene_exp.diff or something like that which has the results of the statistical test. Sort by qvalue and chose a cutoff you like. Is that what you are asking?
You can then take your significantly expressed gene list and feed that into goseq if you want to do gene ontology analysis.
Leave a comment:
-
There should be a file gene_exp.diff or something like that which has the results of the statistical test. Sort by qvalue and chose a cutoff you like. Is that what you are asking?
You can then take your significantly expressed gene list and feed that into goseq if you want to do gene ontology analysis.
Leave a comment:
-
This is a very good tutorial here, but it still leaves some questions unanswered.
How do you determine what cuffdiff lists as noteworthy genes for upregulation or downregulated? I am only seeing the FPKM for each gene and the lo and high confidence. How can I see the genes that are predicted to be noteworthy as mentioned in this tutorial?
This author took the log2 of all FPKM values? Isn't the FPKM a value of within samples expression compared to overall transcript numbers?
I would also like to know what scripts or programs did he run in R?
Any guidance or other tutorials that will lead me forward after obtaining cuffdiff file would be helpful. I have four samples and run cuffdiff with tophat bam files for each and the chicken annotation gtf.
Thanks!
Leave a comment:
-
Hi Bjorn,Originally posted by usad View PostHi
whilst you get much further with the command line, you can always try out our tool RobiNA http://mapman.gabipd.org/web/guest/robin which will give you a graphical user interface and run all necessary steps in the background to call differential expression. It also comes with a long manual.
Apart from that you might check out the tutorials in the seqanswers for running your data through.
Cheers,
björn
Thank you for the reply. And for the link on this tool. I already have the cuffdiff output and I would use command line but I am wondering where to begin. How do I retrieve all of the differential regulated genes or transcripts?
-Tom
Leave a comment:
-
yes, I have used cummeRbund to plot some of the graphs. Which look nice, but I am more curious in pulling out differential expressed genes. I would like to look at the data globally vs. picking and choosing genes. From my use of cummeRbund, I was able to obtain plots which show differences and similarities between samples however, I wasn't able to see where those differences were located (i.e., specific genes or novel transcripts) - just dots on a graph. Maybe I am missing the feature that allows one to export the transcripts or genes that are upregulated or downregulated x-fold from the control or other samples.Originally posted by ETHANol View PostcumbRbund is the next step in the tuxedo suite. After that it all depends on what you want to do.
Leave a comment:
-
Hi
whilst you get much further with the command line, you can always try out our tool RobiNA http://mapman.gabipd.org/web/guest/robin which will give you a graphical user interface and run all necessary steps in the background to call differential expression. It also comes with a long manual.
Apart from that you might check out the tutorials in the seqanswers for running your data through.
Cheers,
björn
Leave a comment:
-
cumbRbund is the next step in the tuxedo suite. After that it all depends on what you want to do.
Leave a comment:
-
RNAseq data analysis
I recently started some RNAsequencing of tumor samples. My main question is regarding the differential gene expression among samples and controls. I have successful utilized tophat, cufflinks, and cuffdiff. I am new to bioinformatics and RNAseq analysis. My experience utilizing Linux terminals for analysis is only recent. I have seen a few tutorials online for RNAseq, but some of them only take you through the cufflinks data retrieval. I am looking for what next....the steps and analysis after cuffdiff. Are there programs that exist or tutorials that exist for running a script in python or R for analysis of the data? How do others go about analyzing RNAseq data for differential expression among samples?
Any advice on the downstream analysis of RNAseq data after the tuxedo suite would be greatly appreciated.
Thanks!Tags: None
Latest Articles
Collapse
-
by SEQadmin2
Tumors contain complex mixtures of cell populations that evolve in response to treatment and host-specific factors. Tissue biopsies provide only static snapshots of a tumor’s state. But what if we could follow that evolution over time using a minimally invasive technique?
Liquid biopsies can detect tumor-derived material circulating in the bloodstream, providing a way to study treatment response, detect emerging resistance, and discover new biomarkers. Circulating...-
Channel: Articles
10-14-2026, 09:55 AM -
-
by SEQadmin2
Researchers using sequencing and genomics tools often have to make trade-offs. They can choose between speed or scale, short reads or long-range information, or targeted panels or a view of the whole transcriptome. New technologies that have been released this year are built to address those tough choices.
We asked six companies the same four questions to learn about their latest products. The new technologies bring a lot to the table, including rethinking sequencing...-
Channel: Articles
-
ad_right_rmr
Collapse
News
Collapse
| Topics | Statistics | Last Post | ||
|---|---|---|---|---|
|
Started by SEQadmin2, Yesterday, 11:13 AM
|
0 responses
16 views
0 reactions
|
Last Post
by SEQadmin2
Yesterday, 11:13 AM
|
||
|
Started by SEQadmin2, Yesterday, 10:48 AM
|
0 responses
17 views
0 reactions
|
Last Post
by SEQadmin2
Yesterday, 10:48 AM
|
||
|
Started by SEQadmin2, 10-15-2026, 10:52 AM
|
0 responses
35 views
0 reactions
|
Last Post
by SEQadmin2
10-15-2026, 10:52 AM
|
||
|
Started by SEQadmin2, 10-14-2026, 05:39 AM
|
0 responses
42 views
0 reactions
|
Last Post
by SEQadmin2
10-14-2026, 05:39 AM
|
Leave a comment: