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Job:
Postdoc+PhD position: AI large-language models of single-cell data for cancer immunogenomics
JobPosting
AI
HPC
CuratedAtlasQueryR
10 months ago
Stefano Mangiola
▴ 40
5
votes
25
replies
2.4k
views
limma models out of memory issue on Slurm HPC
Regression
limma
STATISITICS
HPC
updated 13 months ago by
Gordon Smyth
52k • written 13 months ago by
Jitendra
▴ 10
0
votes
0
replies
600
views
Fatal error: Wrong thread calling 'RunFinalizers'
featureCount
Rsubread
HPC
19 months ago
kthapa
• 0
4
votes
8
replies
3.7k
views
R package installation error
HPC
R
Bioconducter
3.1 years ago
Jitendra
▴ 10
0
votes
0
replies
688
views
Profiling bioconductor packages in a straightforward fashion
HPC
profiling
performance
3.5 years ago
Jack
• 0
2
votes
2
replies
1.8k
views
Problem installing Minfi on Cluster
Minfi
local installation
Centos
hpc
updated 7.0 years ago by
Kasper Daniel Hansen
★ 6.5k • written 7.0 years ago by
Goku
• 0
6 results • Page
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Replies
Comment: How to left_join a tidySummarizedExperiment with a GRanges object by seqnames an
by
James W. MacDonald
68k
Have you figured out how to do this using tidy grammar? Using non-tidy grammar is quite simple, and perhaps you already know how to do that…
Comment: How can I correctly use phyloseq with Docker?
by
James W. MacDonald
68k
You can use [bioc-run][1] to simplify things as well. [1]: https://github.com/Bioconductor/bioc-run/tree/devel
Comment: How can I correctly use phyloseq with Docker?
by
James W. MacDonald
68k
You show how you modified the container, but not how you are running it, which is the critical part.
Comment: Discrepancies in normalised count data vs unnormalised
by
AMgroup
• 0
Thank you for your reply. > Per sample all counts are scaled by the same size factor so I strongly assume that something was parsed here …
Comment: Discrepancies in normalised count data vs unnormalised
by
ATpoint
★ 4.8k
Please show examples using `plotCounts()`. Custom spreadsheets harbor the risk of parsing errors along the way which very often explains wh…
Votes
Answer: How to combine two DESeq2 objects (dds) for analysis
How to combine two DESeq2 objects (dds) for analysis
How can I correctly use phyloseq with Docker?
A: DESeq2::sizeFactors() function does not output the sizeFactor table.
Comment: Filtering after DESeq
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