Log In
Sign Up
about
faq
Ask a question
Latest
News
Jobs
Tutorials
Tags
Users
New Post
Latest
News
Jobs
Tutorials
Tags
Users
Log In
Sign Up
About
Limit
all time
today
this week
this month
this year
Unanswered
All posts
Sort
Update
Answers
Bookmarks
Creation
Replies
Rank
Views
Votes
Showing :
variantannotation
•
reset
1
vote
4
replies
5.1k
views
merging VCF files
VariantAnnotation
VariantAnnotation
VariantAnnotation
VariantAnnotation
written 10.3 years ago by
Valerie Obenchain
★ 6.8k
1
vote
2
replies
4.3k
views
ICU init failed: U_FILE_ACCESS_ERROR while loading library "VariantAnnotation"
variantannotation
library
error
updated 7.8 years ago by
Valerie Obenchain
★ 6.8k • written 7.8 years ago by
kmu004
▴ 50
2
votes
2
replies
4.2k
views
Add data to Vcf Info Field
variantannotation
updated 8.6 years ago by
Valerie Obenchain
★ 6.8k • written 8.6 years ago by
Moiz Bootwalla
▴ 50
0
votes
4
replies
4.1k
views
Question: How can I filter a vcf file by DP and GQ using the R package VariantAnnotation?
VariantAnnotation
Sample Read Depth
Phred-Scaled Genotype Quality
vcf
updated 8.2 years ago by
Valerie Obenchain
★ 6.8k • written 8.2 years ago by
r.jaffe
• 0
1
vote
5
replies
3.7k
views
Converting a DNAStringSetList to characters quickly
readVcf
DNAStringSet
DNAStringSetList
variantannotation
readvcf
8.1 years ago
dan.gatti
• 0
0
votes
2
replies
3.5k
views
VariantAnnotation R Package - Merging Two VCF files
VariantAnnotation
VariantAnnotation
VariantAnnotation
VariantAnnotation
written 9.3 years ago by
Fong Chun Chan
▴ 320
0
votes
21
replies
3.4k
views
VariantAnnotation Errors and void outputs
variantannotation
readvcf
8.1 years ago • updated 8.0 years ago
pifferdavide
• 0
0
votes
1
reply
3.2k
views
Subset VCF files using multiple criteria
vcf
variantannotation
granges
7.3 years ago
georgewwp
• 0
3
votes
4
replies
3.1k
views
Quality filtering of exactSNP-generated VCF files
exactSNP
qc
variantannotation
updated 8.6 years ago by
Wei Shi
★ 3.5k • written 8.6 years ago by
daniel.silvestre
▴ 100
0
votes
1
reply
3.0k
views
Multi-sample VCF file and filterVcf
VariantAnnotation
Annotation
VariantAnnotation
VariantAnnotation
Annotation
VariantAnnotation
updated 9.1 years ago by
Valerie Obenchain
★ 6.8k • written 9.1 years ago by
Guest User
★ 12k
2
votes
6
replies
2.9k
views
Import of vcf with VariantAnnotation
variantannotation
somaticsignatures
8.6 years ago
Anna N.
• 0
5
votes
6
replies
2.8k
views
Error in reading 1000 genomes data
variantannotation
updated 7.3 years ago by
Martin Morgan
25k • written 8.6 years ago by
Wade Copeland
▴ 20
0
votes
2
replies
2.8k
views
Problem reading VCF file using readVcf from package VariantAnnotation
VariantAnnotation
VariantAnnotation
VariantAnnotation
VariantAnnotation
updated 10.1 years ago by
Valerie Obenchain
★ 6.8k • written 10.1 years ago by
UBodenhofer
▴ 290
3
votes
5
replies
2.6k
views
Add Custom Annotations to Multi-Sample VCF with VariantAnnotation() package
variantannotation
granges
DNAStringSetList
findoverlaps
Vranges
8.3 years ago
summerela
• 0
1
vote
12
replies
2.5k
views
VariantAnnotation: no method for function 'path' for signature 'character'
variantannotation
readvcf
readgt
updated 8.5 years ago by
Valerie Obenchain
★ 6.8k • written 8.5 years ago by
Kipper Fletez-Brant
▴ 150
0
votes
2
replies
2.5k
views
Problem using biocLite() to update packages
biocLite
BiocInstaller
variantannotation
updated 5.6 years ago by
James W. MacDonald
63k • written 5.6 years ago by
Jenny Drnevich
★ 2.0k
3
votes
9
replies
2.5k
views
Annotate VCFs with Cosmic (ExAC etc.) fields
variantannotation
cosmic
exac
updated 6.6 years ago by
Martin Morgan
25k • written 6.6 years ago by
markus.riester
▴ 130
1
vote
7
replies
2.4k
views
Data from ##SAMPLE lines in VCF?
variantannotation
coldata
updated 4.7 years ago by
Valerie Obenchain
★ 6.8k • written 4.7 years ago by
lvclark
▴ 10
0
votes
10
replies
2.4k
views
Incorrect row names when a VCF has multiple ALTs.
variantannotation
vcf
updated 8.6 years ago by
Valerie Obenchain
★ 6.8k • written 8.6 years ago by
bicycle1885
• 0
4
votes
10
replies
2.4k
views
Best way to import from multiple VCF files?
variantannotation
updated 6.9 years ago by
shepherl
3.5k • written 6.9 years ago by
Kipper Fletez-Brant
▴ 150
0
votes
7
replies
2.3k
views
VariantAnnotation: Performance and memory issues in readVcf
VariantAnnotation
PROcess
Rsamtools
VariantAnnotation
VariantAnnotation
PROcess
Rsamtools
updated 10.1 years ago by
Vincent J. Carey, Jr.
6.6k • written 10.1 years ago by
UBodenhofer
▴ 290
0
votes
8
replies
2.3k
views
Best practices to find intersection among variants
VariantAnnotation
genomes
VariantAnnotation
VariantAnnotation
genomes
VariantAnnotation
updated 8.8 years ago by
Julian Gehring
★ 1.3k • written 8.8 years ago by
Marco Blanchette
▴ 220
0
votes
7
replies
2.3k
views
append to bgzipped VCF file
variantannotation
tabix
updated 7.6 years ago by
Michael Lawrence
11k • written 7.6 years ago by
TimothéeFlutre
▴ 80
2
votes
5
replies
2.2k
views
Plot data from VCF using Gviz?
gviz
variantannotation
vcf
updated 7.6 years ago by
Valerie Obenchain
★ 6.8k • written 7.6 years ago by
Johannes Rainer
★ 2.0k
0
votes
1
reply
2.2k
views
help with analysis of genotyping data from Illumina HumanOmni5-4v1_B chip
SNP
VariantAnnotation
Annotation
probe
VariantAnnotation
GWASTools
SNP
VariantAnnotation
updated 9.0 years ago by
Stephanie M. Gogarten
▴ 840 • written 9.0 years ago by
Abhishek Pratap
▴ 160
2
votes
9
replies
2.2k
views
ReadVCF not reading samples
readvcf
vcf
variantannotation
8.0 years ago
askates
▴ 10
2
votes
2
replies
2.2k
views
Vranges (somatic signature) VariantAnnotation
software error
variantannotation
updated 8.6 years ago by
Steve Lianoglou
13k • written 8.6 years ago by
humaasif79
• 0
2
votes
5
replies
2.1k
views
VariantAnnotation: Error with ScanVcfParam
variantannotation
vcf
readvcf
filtervcf
scanvcfparam
5.8 years ago
Didi
▴ 10
0
votes
2
replies
2.1k
views
merging VCF files
VariantAnnotation
VariantAnnotation
VariantAnnotation
VariantAnnotation
written 10.4 years ago by
Stephanie M. Gogarten
▴ 840
2
votes
6
replies
2.1k
views
extracting Allele Read Counts - part2
rsamtools
variantannotation
updated 6.2 years ago by
James W. MacDonald
63k • written 6.2 years ago by
Bogdan
▴ 660
3
votes
8
replies
2.0k
views
Create protein sequences including variants from a VCF file
VariantAnnotation
customProDB
4.3 years ago • updated 4.2 years ago
daniel.magnus.bader
▴ 40
0
votes
6
replies
2.0k
views
readVcf shape of 'skeleton' is not compatible with 'NROW(flesh)'
variantannotation
updated 8.0 years ago by
Valerie Obenchain
★ 6.8k • written 8.0 years ago by
Miss Agnieszka Aleksandra Golicz
▴ 40
0
votes
2
replies
2.0k
views
VariantAnnotation Installation Error RSQLite
VariantAnnotation
RSQLite
8.5 years ago
remi.tournebize
▴ 10
1
vote
12
replies
1.9k
views
readVcf does not recognize tabix index
VariantAnnotation
readvcf
tabix
updated 2.2 years ago by
Vincent J. Carey, Jr.
6.6k • written 2.2 years ago by
naive
• 0
1
vote
10
replies
1.9k
views
predictCoding error DNAStringSet_translate
variantannotation
predict coding
updated 8.2 years ago by
Valerie Obenchain
★ 6.8k • written 8.2 years ago by
Miss Agnieszka Aleksandra Golicz
▴ 40
0
votes
17
replies
1.9k
views
problems with strand in predictCoding
VariantAnnotation
Annotation
BSgenome
BSgenome
VariantAnnotation
VariantAnnotation
BSgenome
updated 11.1 years ago by
bnorthoff@web.de
▴ 20 • written 11.1 years ago by
Jeremiah Degenhardt
▴ 50
0
votes
20
replies
1.9k
views
VariantAnnotation function getTranscriptSeqs() gives error "object '.makeUCSCTxListFromGRangesList' not found"
variantannotation
7.8 years ago • updated 7.6 years ago
Tjeerd Dijkstra
• 0
3
votes
3
replies
1.9k
views
VariantAnnotation Installation Failure
VariantAnnotation
updated 6.0 years ago by
Valerie Obenchain
★ 6.8k • written 6.0 years ago by
andrew.j.skelton73
▴ 360
0
votes
3
replies
1.9k
views
vcf postion extract
vcf
variantannotation
position
updated 7.4 years ago by
Martin Morgan
25k • written 7.4 years ago by
1000G_Q
• 0
2
votes
3
replies
1.8k
views
Metadata Missing from vcf when reading in with readVcfAsVRanges
variantannotation
vranges
readvcf
readvcfasvranges
metadata
8.3 years ago
summerela
• 0
0
votes
23
replies
1.8k
views
VariantAnnotation geno function
variantannotation
6.6 years ago
ribioinfo
▴ 100
1
vote
4
replies
1.8k
views
variantAnnotation::locateVariants() with AllVariants(): why do some input variants not get annotated?
variantannotation
locatevariants
7.8 years ago
Jakob Goldmann
• 0
0
votes
5
replies
1.7k
views
Error installing VariantAnnotation with bioconductor/devel_core
install
variantannotation
8.3 years ago
kforner
• 0
0
votes
4
replies
1.7k
views
'namespace:Biostrings' error when installing VariantAnnotation
VariantAnnotation
VariantAnnotation
VariantAnnotation
VariantAnnotation
updated 10.0 years ago by
Steve Lianoglou
13k • written 10.0 years ago by
Thomas Damm Als
▴ 20
4
votes
4
replies
1.7k
views
readVcfAsVRanges + FilterRules
variantannotation
filterVcf
readvcfasvranges
filterRules
updated 8.3 years ago by
Martin Morgan
25k • written 8.3 years ago by
Sigve Nakken
▴ 50
0
votes
3
replies
1.7k
views
trouble installing affycoretools for R 3.0
VariantAnnotation
GO
BSgenome
affycoretools
BSgenome
VariantAnnotation
ggbio
GO
BSgenome
updated 10.2 years ago by
James W. MacDonald
63k • written 10.2 years ago by
Jenny Drnevich
★ 2.0k
0
votes
6
replies
1.7k
views
Error using readVcf
gwastools
variantannotation
updated 6.0 years ago by
Stephanie M. Gogarten
▴ 840 • written 6.0 years ago by
Lna
• 0
1
vote
3
replies
1.7k
views
annotation of SV (Structural Variants)
variantannotation
annotationhub
6.2 years ago
Bogdan
▴ 660
1
vote
23
replies
1.7k
views
Distance calculation for variants in intergenic regions
locatevariants
variantannotation
genomicfeatures
updated 6.6 years ago by
Michael Lawrence
11k • written 6.6 years ago by
Lna
• 0
0
votes
5
replies
1.7k
views
VariantAnnotation _ problem in merging files, mutationspectrum per sample
variantannotation
updated 8.5 years ago by
Julian Gehring
★ 1.3k • written 8.5 years ago by
Anna N.
• 0
50 results • Page
1 of 1
Recent ...
Replies
Comment: Interpret plot from DiffBind
by
Rory Stark
★ 4.9k
See above, you want the sites where `Fold > 0`.
Comment: Interpret plot from DiffBind
by
Rory Stark
★ 4.9k
That does seem like you have a very high number of open chromatin sites changing. How many are in the consensus matrix? You can see how ma…
Comment: Interpret plot from DiffBind
by
Rory Stark
★ 4.9k
I can see the confusion here as one color is being used in two different ways. The dark blue/purple color is used for the bars on the left…
Comment: P-value histogram of testLinearModel is not uniform
by
ATpoint
★ 2.9k
The work from @csoneson (https://pubmed.ncbi.nlm.nih.gov/29481549/) points out that for scRNA-seq a good prefiltering improves DE reliabili…
Answer: Diffbind "No genome detected"
by
Rory Stark
★ 4.9k
In this case, `DiffBind` is unable to automatically determine the genome from the supplied Input bam file. You should be able to specify `g…
Votes
Answer: Using PEER to identify hidden confounders in RNA-seq data (not working)
Answer: Using PEER to identify hidden confounders in RNA-seq data (not working)
Answer: P-value histogram of testLinearModel is not uniform
Answer: Interpret plot from DiffBind
C: Minimum number of samples per treatment/group for WGCNA analysis
Awards
• All
Popular Question
to
rodrigo.duarte88
▴ 30
Scholar
to
Rory Stark
★ 4.9k
Popular Question
to
arfranco
▴ 130
Popular Question
to
Johannes Rainer
★ 2.0k
Popular Question
to
Jenn
▴ 30
Locations
• All
United States,
9 minutes ago
France,
10 minutes ago
Russia,
17 minutes ago
United States,
19 minutes ago
Netherlands,
22 minutes ago
Traffic: 577 users visited in the last hour
Content
Search
Users
Tags
Badges
Help
About
FAQ
Access
RSS
API
Stats
Use of this site constitutes acceptance of our
User Agreement and Privacy Policy
.
Powered by the
version 2.3.6