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Seqnames
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0
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5
replies
4.4k
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Grange object subsetting using seqnames
Seqnames
makeGRangesFromDataFrame
GRanges
Subsetting
GenomicRanges
4.3 years ago
rtrivedi1
▴ 10
2
votes
1
reply
1.1k
views
DNAStringSet to DNAStringSetList according to pattern in sequence names
dnastringset
dnastringsetlist
seqnames
6.9 years ago
s.ghignone
▴ 10
0
votes
1
reply
1.3k
views
GenomeInfoDb: where are the genome patches?
seqnames
genomeinfodb
updated 8.4 years ago by
Hervé Pagès
16k • written 8.4 years ago by
matt.chambers42
▴ 10
0
votes
2
replies
2.3k
views
GenomicRanges: `seqnames<-` can not work as expected
genomicranges
seqnames
factor
8.9 years ago
wcstcyx
▴ 30
0
votes
1
reply
1.1k
views
error in noGGi
software error
seqnames
characters
r
chipseq
9.4 years ago
awakumaya
• 0
17
votes
4
replies
18k
views
How to properly sort GRanges?
granges
genomicranges
sort
seqnames
order
updated 10.5 years ago by
yinghua
▴ 30 • written 10.9 years ago by
enricoferrero
▴ 680
0
votes
6
replies
7.2k
views
GRanges: problem with multiple seqnames and seqlengths
GRanges
seqnames
seqlengths
IRanges
11.0 years ago
topher.hamm
• 0
7 results • Page
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Comment: Error Loading Experiment from SimBenchData Package
by
ATpoint
★ 4.9k
Is the Seurat package installed? The error somewhat suggests that it could be related, and at https://www.bioconductor.org/packages/release…
Answer: Help with defining groups
by
Gordon Smyth
53k
Defining sample groups is separate to reading in the DIA-NN data, because the sample conditions and covariates are not necessarily coded in…
Comment: Sharing a collection of datasets in ExperimentHub
by
Peter Hickey
▴ 760
The [**scRNAseq**](https://bioconductor.org/packages/scRNAseq/) package ([source on GitHub](https://github.com/LTLA/scRNAseq)) might serve …
Comment: Using DESeq2 on single cell RNA Seq data of same cell type but different conditi
by
ReinholdGaylord99
• 0
Thank you so much! https://www.nature.com/articles/s41467-021-25960-2/ [geometry dash lite](https://geometrydashlite.online)
Comment: Guidance on limma for pseudobulk scRNA-seq with multi-factor design
by
Gordon Smyth
53k
I'm not sure that I understand. You have a dataset that, even after pseudo-bulking, still has 6000 samples? That is surprising. Retaining …
Votes
Answer: Expected memory usage for analyzing large single-cell seq datasets (> 450,000 ce
Answer: ordinary t from limma [was: How would I normally compare swirl?]
Comment: readDNAStringSet with non DNA characters
Comment: Guidance on limma for pseudobulk scRNA-seq with multi-factor design
Answer: Guidance on limma for pseudobulk scRNA-seq with multi-factor design
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