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locatevariants
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4
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8
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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
2.7 years ago
davidhillis
• 0
0
votes
1
reply
938
views
Information about locateVariants function
genomiclocation
canonicaltranscripts
locateVariants
updated 4.2 years ago by
James W. MacDonald
68k • written 4.2 years ago by
Paola
• 0
2
votes
2
replies
2.0k
views
[VariantAnnotation] Preserve query metadata with locateVariants()
variantannotation
locatevariants
metadata
mcols
updated 8.0 years ago by
Valerie Obenchain
★ 6.8k • written 8.0 years ago by
enricoferrero
▴ 680
0
votes
1
reply
1.5k
views
predictCoding errors with: sequence ^1$ not found
variantannotation
predict coding
locateVariants
granges
8.1 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
8.3 years ago
Aleksandra
• 0
0
votes
2
replies
2.0k
views
SNPs in multiple locations
txdb.hsapiens.ucsc.hg19.knowngene
ucsc
annotation
locatevariants
variantannotation
updated 8.4 years ago by
Valerie Obenchain
★ 6.8k • written 8.4 years ago by
Lna
• 0
1
vote
23
replies
3.8k
views
Distance calculation for variants in intergenic regions
locatevariants
variantannotation
genomicfeatures
updated 9.1 years ago by
Michael Lawrence
★ 11k • written 9.1 years ago by
Lna
• 0
1
vote
4
replies
2.7k
views
variantAnnotation::locateVariants() with AllVariants(): why do some input variants not get annotated?
variantannotation
locatevariants
10.3 years ago
Jakob Goldmann
• 0
8 results • Page
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Comment: GOseq Probability Weight Function bad fit
by
ejasge.r.m
• 0
When performing GO analysis with GOseq, i s important to carefully check your input and assumptions, just like reviewing choices on the McD…
Answer: problem reading bam files into nucleR
by
James W. MacDonald
68k
The first step is to update to the current versions of R/Bioconductor and try again. It's possible that you have run into a bug that's alre…
Answer: Question about DESeq2 Design for Paired Treatment Study
by
ATpoint
★ 5.0k
It's a paired analysis so you don't need any patient-specific covariates such as age and sex. What you call batch effect might just be the …
Comment: problem reading bam files into nucleR
by
efoss
▴ 10
I thought I might be able to track down a problematic line in the bam file by repeatedly splitting the bam file in and then running the co…
Answer: two questions about limma
by
Gordon Smyth
53k
Answered here: https://support.bioconductor.org/p/16318/
Votes
Upcoming Ensembl API and data access changes - new blog post available
Comment: Highly similar RNA-seq samples in PCA - pooling or technical duplication?
Answer: Large logFC but somewhat high FDR
Comment: upstream git branches of bioc-release
Comment: upstream git branches of bioc-release
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