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genomeintervals
•
reset
0
votes
0
replies
816
views
Using Granges to find overlapping pairs at exactly 10kb distance
genomeIntervals
GenomicRanges
21 months ago
gshweta95
• 0
2
votes
3
replies
1.9k
views
GRanges object from gene list
granges
bed
genomicranges
genomeintervals
deseq2
8.0 years ago
rbronste
▴ 60
2
votes
1
reply
2.1k
views
Extracting UTRs from exon and CDS data
genomeintervals
UTRs
exons
CDS
GenomicRanges
updated 8.5 years ago by
Michael Lawrence
★ 11k • written 8.5 years ago by
rubi
▴ 110
3
votes
2
replies
1.8k
views
What is the main difference between nclist and intervaltree algorithm in GenomicRanges packages ?
nclist
genomeintervals
updated 10.0 years ago by
Hervé Pagès
16k • written 10.0 years ago by
Jurat Shahidin
▴ 80
0
votes
1
reply
1.5k
views
cannot load genomeIntervals package
genomeIntervals
updated 10.6 years ago by
Nicolas Delhomme
▴ 320 • written 10.8 years ago by
mhz
• 0
1
vote
8
replies
2.4k
views
Bug: readGff3 isRightOpen should be FALSE
genomeintervals
updated 10.6 years ago by
Nicolas Delhomme
▴ 320 • written 10.6 years ago by
sjackman
• 0
0
votes
1
reply
3.0k
views
biocLite("TxDb.Hsapiens.UCSC.hg19.knownGene") fails
BSgenome
hexbin
BSgenome
IRanges
genomeIntervals
GenomicRanges
girafe
Rsamtools
HiTC
HiTC
updated 12.8 years ago by
Dan Tenenbaum
★ 8.2k • written 12.8 years ago by
Wim Kreinen
▴ 100
0
votes
0
replies
1.2k
views
convert "Genome_intervals_stranded" to "Genome_intervals"? (girafe)
Annotation
convert
genomeIntervals
Annotation
convert
genomeIntervals
13.9 years ago
delhomme@embl.de
★ 1.2k
0
votes
1
reply
1.3k
views
gff files: how to tell if right-open interval convention used?
genomeIntervals
genomeIntervals
updated 14.8 years ago by
Hervé Pagès
16k • written 14.8 years ago by
Julien Gagneur
▴ 50
0
votes
0
replies
1.4k
views
stranded findOverlaps
Sequencing
Annotation
GO
rtracklayer
IRanges
genomeIntervals
Sequencing
Annotation
GO
16.0 years ago
Robert Castelo
★ 3.4k
10 results • Page
1 of 1
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Comment: Clarification on counting in Rsubread (featureCounts)
by
Gordon Smyth
53k
Your follow-up question is very much wider than the first, and is essentially a research question rather a software question. As one of the…
Comment: Error in creating BSGenome package
by
Nguyen
• 0
I keep running into this error, please help: ``` Writing all sequences to './BSgenome.Panubis.NCBI.Panubis1.0/inst/extdata/single_sequenc…
Comment: Joining different datasets and analyzing using the group-specific condition effe
by
James W. MacDonald
68k
There is an example of how you can do this in the [DESeq vignette][1]. An alternative would be to fit a linear mixed model using the `vari…
Comment: Joining different datasets and analyzing using the group-specific condition effe
by
jason.chai
• 0
@mikelove Could I please ask if a similar method would work my set of samples? I have 255 samples which have been generated from 76 subject…
Comment: Clarification on counting in Rsubread (featureCounts)
by
Luca
• 0
Thanks to both of you for your helpful suggestions. The counting was already strand-specific at both the exon and gene levels. I resolved …
Votes
A: DESeq2: What is the unit of DESeq2 normalized read count (VST)? Is it tag per mi
Answer: Clarification on counting in Rsubread (featureCounts)
Comment: Clarification on counting in Rsubread (featureCounts)
C: ControlGenes/ housekeeping genes Deseq2
Answer: Clarification on counting in Rsubread (featureCounts)
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53k
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