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Showing :
variantAnnotation
•
reset
0
votes
2
replies
1.7k
views
VariantAnnotation::locateVariants error coming from XVector
variantannotation
xvector
iranges
7.6 years ago • updated 7.5 years ago
Vivek.b
▴ 100
0
votes
2
replies
2.4k
views
filtering a VCF file based on genotype
variantannotation
updated 7.6 years ago by
Valerie Obenchain
★ 6.8k • written 7.6 years ago by
Bogdan
▴ 670
0
votes
1
reply
1.8k
views
VariantAnnotation and filtering a VCF
variantannotation
7.6 years ago
Bogdan
▴ 670
0
votes
1
reply
1.6k
views
Annotating outdated SNP identifiers
variants
variantannotation
SNPlocs.Hsapiens.dbSNP150.GRCh38
biomaRt
7.8 years ago
sandmann.t
▴ 70
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
2
replies
3.4k
views
Problem using biocLite() to update packages
biocLite
BiocInstaller
variantannotation
updated 8.1 years ago by
James W. MacDonald
68k • written 8.1 years ago by
Jenny Drnevich
★ 2.0k
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
7
votes
4
replies
2.8k
views
BiocGenerics built with R 3.4.2 changes behaviour
biocgenerics
iranges
variantannotation
updated 8.2 years ago by
Hervé Pagès
16k • written 8.2 years ago by
ginggs
▴ 40
7
votes
6
replies
2.4k
views
SNP location annotation problem in "VariantAnnotation" package
annotation
variantannotation
updated 8.3 years ago by
Valerie Obenchain
★ 6.8k • written 8.3 years ago by
yduan004
▴ 20
0
votes
4
replies
1.9k
views
Translation Error in predictCoding() for VariantAnnotation
VariantAnnotation
updated 8.3 years ago by
Hervé Pagès
16k • written 8.3 years ago by
creasyt
• 0
8
votes
6
replies
2.7k
views
Error when running "locateVariants" function in "VariantAnnotation" package
variantannotation
tidyverse
genomicfeatures
updated 8.3 years ago by
Hervé Pagès
16k • written 8.3 years ago by
yduan004
▴ 20
0
votes
2
replies
2.1k
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
1
reply
1.8k
views
Troubleshooting a histogram DataTrack in Gviz
VariantAnnotation
gviz
8.4 years ago
Russ Fraser
▴ 40
2
votes
5
replies
3.4k
views
VariantAnnotation: Error with ScanVcfParam
variantannotation
vcf
readvcf
filtervcf
scanvcfparam
8.4 years ago
Didi
▴ 10
0
votes
2
replies
2.0k
views
SNPs in multiple locations
txdb.hsapiens.ucsc.hg19.knowngene
ucsc
annotation
locatevariants
variantannotation
updated 8.5 years ago by
Valerie Obenchain
★ 6.8k • written 8.5 years ago by
Lna
• 0
0
votes
1
reply
1.1k
views
summarizeVariants from VariantAnnotation reordering genes in rownames
variantannotation
summarizevariants
updated 8.5 years ago by
Valerie Obenchain
★ 6.8k • written 8.5 years ago by
Todd Creasy
• 0
3
votes
4
replies
2.0k
views
No annotation for single SNPs
variantannotation
SNPs
txdb.hsapiens.ucsc.hg19.knowngene
ucsc
updated 8.5 years ago by
Valerie Obenchain
★ 6.8k • written 8.5 years ago by
Lna
• 0
0
votes
6
replies
3.1k
views
Error using readVcf
gwastools
variantannotation
updated 8.5 years ago by
Stephanie M. Gogarten
▴ 890 • written 8.5 years ago by
Lna
• 0
3
votes
3
replies
3.0k
views
VariantAnnotation Installation Failure
VariantAnnotation
updated 8.6 years ago by
Valerie Obenchain
★ 6.8k • written 8.6 years ago by
andrew.j.skelton73
▴ 370
1
vote
2
replies
1.2k
views
Exclude Mutations from Mutation List
variantannotation
updated 8.6 years ago by
Martin Morgan
25k • written 8.6 years ago by
Haiying.Kong
▴ 110
2
votes
6
replies
3.5k
views
extracting Allele Read Counts - part2
rsamtools
variantannotation
updated 8.7 years ago by
James W. MacDonald
68k • written 8.7 years ago by
Bogdan
▴ 670
0
votes
3
replies
1.5k
views
Error in c(DataFrameList(META = meta), tbls[unique(tags)])
VariantAnnotation
updated 8.7 years ago by
Hervé Pagès
16k • written 8.7 years ago by
ddzhangzz
• 0
1
vote
3
replies
2.6k
views
annotation of SV (Structural Variants)
variantannotation
annotationhub
8.7 years ago
Bogdan
▴ 670
3
votes
2
replies
2.0k
views
filtering VCF files
variantannotation
variantfiltering
updated 8.7 years ago by
Michael Lawrence
★ 11k • written 8.7 years ago by
Bogdan
▴ 670
0
votes
0
replies
1.3k
views
VariantAnnotation mapToTranscripts: best implementation
VariantAnnotation
mapToTranscripts
8.8 years ago
kristina_holton
• 0
0
votes
2
replies
1.4k
views
does readVcf mistakenly ignore ploidy for missing genotypes?
readvcf
gt
missing
VariantAnnotation
8.8 years ago
TimothéeFlutre
▴ 80
2
votes
7
replies
2.7k
views
VariantAnnotation - expand not working as intended for VCF
variantannotation
updated 8.9 years ago by
Michael Lawrence
★ 11k • written 8.9 years ago by
sebastian.hollizeck
• 0
2
votes
4
replies
2.7k
views
Best way to create a VRanges object from a large VCF file?
variantannotation
readvcf
readvcfasvranges
vcf
updated 8.9 years ago by
Michael Lawrence
★ 11k • written 8.9 years ago by
ruben.drews
• 0
3
votes
3
replies
1.9k
views
CollapsedVCF and ExpandedVCF rownames and vcfs with large ref/alt columns
variantannotation
VCF
updated 9.0 years ago by
Valerie Obenchain
★ 6.8k • written 9.0 years ago by
Sean Davis
21k
0
votes
2
replies
1.8k
views
Problem with VariantAnnotation and VCF "R" genotype fields when expanding CollapsedVCF
VariantAnnotation
bug
updated 9.0 years ago by
Valerie Obenchain
★ 6.8k • written 9.0 years ago by
Sean Davis
21k
1
vote
3
replies
1.8k
views
VariantAnnotation error with readVcf after genotypeToSnpMatrix
variantannotation
9.1 years ago
sarah.williams1
▴ 40
0
votes
0
replies
1.5k
views
Job:
PhD Position in Bioinformatics
bioinformatics
protein
variantannotation
data integration
Job
9.1 years ago
stephan.pabinger
• 0
0
votes
1
reply
1.3k
views
VariantAnnotation -filterVcf/FilterRules - 3 fxns as list to FilterRules throughs and erro
filtervcf
variantannotation
updated 9.1 years ago by
Martin Morgan
25k • written 9.1 years ago by
stephen sefick
▴ 60
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
0
votes
7
replies
1.7k
views
VariantAnnotation - filterVcf - Prints multiple vcf headers
variantannotation
updated 9.1 years ago by
Martin Morgan
25k • written 9.1 years ago by
stephen sefick
▴ 60
0
votes
23
replies
3.8k
views
VariantAnnotation geno function
variantannotation
9.1 years ago
ribioinfo
▴ 100
3
votes
9
replies
4.2k
views
Annotate VCFs with Cosmic (ExAC etc.) fields
variantannotation
cosmic
exac
updated 9.1 years ago by
Martin Morgan
25k • written 9.1 years ago by
markus.riester
▴ 130
0
votes
2
replies
1.5k
views
Create VRanges object from mutation data (txt extracted from annotated vcf)
iranges
variantannotation
updated 9.2 years ago by
Michael Lawrence
★ 11k • written 9.2 years ago by
gaiusjaugustus
• 0
2
votes
3
replies
2.0k
views
predictCoding fails with error
VariantAnnotation
9.2 years ago
Stephane Plaisance | VIB |
▴ 60
1
vote
2
replies
1.3k
views
VariantAnnotation CollapsedVCF trouble
variantannotation
subsetting
9.2 years ago
Fabian Grammes
▴ 20
0
votes
1
reply
1.5k
views
SNP Injection in Custom BSGenome
variantannotation
bsgenome
updated 9.3 years ago by
Hervé Pagès
16k • written 9.3 years ago by
michael.weber.1
• 0
1
vote
2
replies
1.5k
views
Locating enhancers that are mutated
snv
granges
genomicranges
variantannotation
indel
updated 9.3 years ago by
Michael Lawrence
★ 11k • written 9.3 years ago by
addyS
• 0
0
votes
0
replies
1.1k
views
After mapping one Sanger sequence read (about 900bp) to hg19 using blastn, How can I get variants presented as reference-based position and base ch…
Biostrings
blast
variantannotation
9.3 years ago
li lilingdu
▴ 450
1
vote
9
replies
1.9k
views
Problem with summarizeVariants function (VariantAnnotation) when using a multi-sample vcf
variantannotation
updated 9.3 years ago by
Valerie Obenchain
★ 6.8k • written 9.4 years ago by
juls
• 0
0
votes
1
reply
1.2k
views
VariantAnnotation print malformated vcf
variantannotation
writevcf
updated 9.4 years ago by
Valerie Obenchain
★ 6.8k • written 9.4 years ago by
ahlberg.gustav
• 0
5
votes
2
replies
1.7k
views
info(header(vcf)) remembers fields not imported: bugfix?
VariantAnnotation
9.4 years ago
kevin.rue
▴ 350
2
votes
2
replies
1.7k
views
readVCFAsVRanges in VariantAnnotation broken by an FTZ format?
variantannotation
readvcfasvranges
vcf
updated 9.4 years ago by
Michael Lawrence
★ 11k • written 9.4 years ago by
Andy Lynch
▴ 120
4
votes
10
replies
4.0k
views
Best way to import from multiple VCF files?
variantannotation
updated 9.4 years ago by
shepherl
4.2k • written 9.4 years ago by
Kipper Fletez-Brant
▴ 150
1
vote
2
replies
1.6k
views
Expand annotation on a vcf file
vcf
variantannotation
updated 9.4 years ago by
Michael Lawrence
★ 11k • written 9.4 years ago by
Dee
• 0
3
votes
8
replies
2.6k
views
Vcf to VRanges conversion error: ["incorrect number of dimensions"]
variantannotation
somaticsignatures
updated 9.4 years ago by
Michael Lawrence
★ 11k • written 9.4 years ago by
maria.vila
• 0
217 results • Page
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Replies
Comment: Bioinformatician at the Lausanne University Hospital
by
eja.ger.m
• 0
For individuals looking to improve communication and collaboration in demanding medical or research environments like the Genetic Medicine …
Answer: NUPOP usage
by
shepherl
4.2k
You should read the documentation in the package especially the package vignette https://bioconductor.org/packages/release/bioc/html/NuPoP.…
Comment: How can I correctly use phyloseq with Docker?
by
fnfgame
• 0
In a rocker image, this error usually means the Bioconductor install happened as root but the runtime library paths used by the shiny user …
Comment: DECIPHER DesignProbes unable to design FISH-probes
by
Erik Wright
▴ 150
Are the sequences aligned (i.e., the same width) before running `TileSeqs()`?
Comment: BiocParallel (and DESeq2) - wrong args for environment subassignment
by
Michael Love
43k
BTW, I tested with no issue on MacOS ARM on our previous github issue.
Votes
C: DESeq2 Following RSEM
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
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