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GenomicInteractions duplicate annotations
duplicate
GenomicInteractions
5.0 years ago
dogancan
• 0
1
vote
3
replies
3.5k
views
duplicated row names when creating DESeqDataSetFromMatrix
deseq2
DESeqDataSetFromMatrix
duplicate
updated 7.1 years ago by
James W. MacDonald
68k • written 7.1 years ago by
Assa Yeroslaviz
★ 1.5k
2
votes
4
replies
1.9k
views
calling combineFeatures twice causes duplicate row.names
msnbase
duplicate
rforproteomics
updated 7.3 years ago by
Laurent Gatto
1.6k • written 7.3 years ago by
joris.vanhoutven
▴ 10
2
votes
1
reply
2.0k
views
How to remmove duplicated paired end alignments
alignment
duplicate
updated 8.3 years ago by
Aaron Lun
★ 28k • written 8.3 years ago by
Frocha
▴ 20
3
votes
16
replies
5.2k
views
Any way to proceed duplicate removal for list of GRanges object ?
r
grangeslist
duplicate
updated 8.3 years ago by
Martin Morgan
25k • written 8.3 years ago by
Jurat Shahidin
▴ 80
3
votes
3
replies
2.3k
views
getBM function, search for annotation characteristics with entrezgene filters --> result with duplicates
getBM
entrez gene identifiers
duplicate
rnaseq
8.3 years ago
Jose Luis Soto Vázquez
• 0
6 results • Page
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Answer: Unable to install a forged BSgenome package
by
James W. MacDonald
68k
Add a repos = NULL to `install.packages`. You may also need to either move the file to a dir that doesn't have a space in the name or you […
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 …
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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