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locateVariants
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reset
4
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8
replies
2.8k
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TxDB.Hsapiens.UCSC.hg38.knownGene with locateVariants() identifying SNPs from various chromosome being part of the same gene
MetID
TxDB.Hsapiens.UCSC.hg38.knownGene
locateVariants
GenomicFeatures
VariantAnnotation
2.5 years ago
davidhillis
• 0
0
votes
1
reply
895
views
Information about locateVariants function
genomiclocation
canonicaltranscripts
locateVariants
updated 4.0 years ago by
James W. MacDonald
68k • written 4.0 years ago by
Paola
• 0
2
votes
2
replies
1.9k
views
[VariantAnnotation] Preserve query metadata with locateVariants()
variantannotation
locatevariants
metadata
mcols
updated 7.8 years ago by
Valerie Obenchain
★ 6.8k • written 7.8 years ago by
enricoferrero
▴ 680
0
votes
1
reply
1.5k
views
predictCoding errors with: sequence ^1$ not found
variantannotation
predict coding
locateVariants
granges
7.9 years ago
tony j
• 0
0
votes
2
replies
2.0k
views
locateVariants function does not find an annotation for the locus
locatevariants
txdb.hsapiens.ucsc.hg19.knowngene
variantannotation
8.1 years ago
Aleksandra
• 0
0
votes
2
replies
1.9k
views
SNPs in multiple locations
txdb.hsapiens.ucsc.hg19.knowngene
ucsc
annotation
locatevariants
variantannotation
updated 8.3 years ago by
Valerie Obenchain
★ 6.8k • written 8.3 years ago by
Lna
• 0
1
vote
23
replies
3.6k
views
Distance calculation for variants in intergenic regions
locatevariants
variantannotation
genomicfeatures
updated 8.9 years ago by
Michael Lawrence
★ 11k • written 8.9 years ago by
Lna
• 0
1
vote
4
replies
2.6k
views
variantAnnotation::locateVariants() with AllVariants(): why do some input variants not get annotated?
variantannotation
locatevariants
10.1 years ago
Jakob Goldmann
• 0
8 results • Page
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Answer: DiffBind - question on the use of filtered or unfiltered input data
by
vejogos850
• 0
DiffBind - question on the use of filtered or unfiltered input data is the best to deal with, and it provides us the solutions that we are …
Answer: Help with defining groups
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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
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The [**scRNAseq**](https://bioconductor.org/packages/scRNAseq/) package ([source on GitHub](https://github.com/LTLA/scRNAseq)) might serve …
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Thank you so much! https://www.nature.com/articles/s41467-021-25960-2/ [geometry dash lite](https://geometrydashlite.online)
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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: 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
Answer: Guidance on limma for pseudobulk scRNA-seq with multi-factor design
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