Showing : VariantAnnotation • reset
4
votes
9
replies
3.1k
views
Create protein sequences including variants from a VCF file
VariantAnnotation customProDB
updated 2 days ago by • 0 • written 5.2 years ago by ▴ 50
0
votes
0
replies
103
views
Cannot use `readVcf()` on a file created with `writeVcf()`
VariantAnnotation
5 weeks ago Stevie Pederson • 0
0
votes
1
reply
161
views
Is random access by row index possible for an indexed VCF file?
Rsamtools VariantAnnotation
updated 9 weeks ago by 65k • written 9 weeks ago by ▴ 180
2
votes
3
replies
1.1k
views
readVcf(remoteFile, "hg19", "region") works on macos, fails on linux and in docker
open.BcfFile VariantAnnotation
updated 4 months ago by • 0 • written 2.9 years ago by ▴ 470
0
votes
0
replies
173
views
RFC: significant changes to ensemblVEP package
VariantAnnotation ensemblVEP
4 months ago Vincent J. Carey, Jr. 6.7k
0
votes
5
replies
502
views
locateVariant from VariantAnnotation returns wrong results
VariantAnnotation locateVariant
updated 5 months ago by 65k • written 5 months ago by ▴ 30
0
votes
0
replies
484
views
Variant Filtering on very large VCF files
VariantAnnotation VariantFiltering
7 months ago Bogdan ▴ 670
2
votes
2
replies
1.5k
views
Matching Variants Between Two VCF Objects
VariantAnnotation
written 3.5 years ago by ★ 1.5k
0
votes
2
replies
562
views
Docker usage with Trio Bioconductor Package
VariantAnnotation docker trio
updated 12 months ago by ★ 4.1k • written 12 months ago by • 0
4
votes
8
replies
1.5k
views
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
14 months ago davidhillis • 0
0
votes
0
replies
499
views
VariantAnnotation::readVcf incorrectly processes GATK Mutect2 vcf INFO field AS_SB_TABLE
vcf AS_SB_TABLE readVcf Mutect2 VariantAnnotation
15 months ago therealgenna • 0
0
votes
3
replies
1.1k
views
Add GP values to VCF
VariantAnnotation
16 months ago Stephanie M. Gogarten ▴ 870
0
votes
1
reply
1.5k
views
Confused about understanding the output and statistics of BAM file after STAR aligning
RNAseq123 VariantFiltering Alignment VariantAnnotation
updated 18 months ago by 65k • written 18 months ago by ▴ 30
2
votes
4
replies
957
views
Error message from protein coding prediction with VariantAnnotation
R VariantAnnotation
20 months ago rwan.work • 0
0
votes
2
replies
760
views
Error message from protein coding prediction with VariantAnnotation
R VariantAnnotation
20 months ago rwan.work • 0
0
votes
2
replies
3.9k
views
VariantAnnotation R Package - Merging Two VCF files
VariantAnnotation VariantAnnotation VariantAnnotation VariantAnnotation
written 10.3 years ago by ▴ 320
0
votes
2
replies
2.6k
views
merging VCF files
VariantAnnotation VariantAnnotation VariantAnnotation VariantAnnotation
written 11.4 years ago by ▴ 870
1
vote
4
replies
5.6k
views
merging VCF files
VariantAnnotation VariantAnnotation VariantAnnotation VariantAnnotation
written 11.3 years ago by ★ 6.8k
0
votes
3
replies
1.0k
views
Problem with intronic variants in VariantAnnotation
VariantAnnotation
updated 2.2 years ago by • 0 • written 2.4 years ago by • 0
0
votes
2
replies
1.1k
views
Reading vcf file with readVcf
VariantAnnotation
2.7 years ago aurelien.dejode • 0
0
votes
2
replies
817
views
Multiple exons for predictCoding() from VariantAnnotation (use phase information from gff3 file)?
VariantAnnotation
updated 2.7 years ago by 16k • written 2.8 years ago by • 0
0
votes
1
reply
895
views
GRanges object out-of-bound
VariantAnnotation
updated 2.7 years ago by 6.7k • written 2.8 years ago by • 0
0
votes
5
replies
1.3k
views
installation error: Error in setIs(class2, cli, extensionObject = obji, doComplete = FALSE and setClass() for chromVAR and VariantAnnotation
Install VariantAnnotation Bioconductor chromVAR
updated 2.7 years ago by 6.7k • written 2.8 years ago by • 0
0
votes
0
replies
612
views
Annotate mutations on DNA level to splice transcripts
VariantAnnotation
2.8 years ago Kasper_holm2 • 0
0
votes
4
replies
1.6k
views
Error of read in large vcf file using readVcf
SomaticSignatures VariantAnnotation
updated 2.9 years ago by 65k • written 2.9 years ago by • 0
0
votes
2
replies
1.2k
views
VariantAnnotation::readVcf not reading variants
VariantAnnotation
updated 3.0 years ago by 65k • written 3.0 years ago by • 0
1
vote
12
replies
3.0k
views
readVcf does not recognize tabix index
VariantAnnotation readvcf tabix
updated 3.1 years ago by 6.7k • written 3.2 years ago by • 0
0
votes
2
replies
2.3k
views
VCF File too large for tabix. Best option to make it usable with R?
samtools tabix VariantAnnotation VCFArray
updated 3.1 years ago by 6.7k • written 3.2 years ago by • 0
0
votes
2
replies
1.3k
views
readVCF requires the argument "genome". What does it stand for?
Genome readVcf VariantAnnotation
3.2 years ago naive • 0
2
votes
2
replies
1.3k
views
Obtaining Comments From VCF Header
VariantAnnotation VCFHeader
updated 3.9 years ago by 25k • written 3.9 years ago by ★ 1.5k
3
votes
2
replies
1.3k
views
Import or Subset VCF PASS Variants
VariantAnnotation subset ScanVcfParam
updated 4.1 years ago by 25k • written 4.1 years ago by ★ 1.5k
0
votes
2
replies
1.1k
views
Extract structural variant and flanking sequence from VCF and fasta, in R
VariantAnnotation Bioconductor VCF Structural variants R
updated 4.1 years ago by 25k • written 4.1 years ago by • 0
0
votes
1
reply
662
views
Can strand be set to minus in VRanges objects?
VariantAnnotation
updated 4.3 years ago by 65k • written 4.3 years ago by • 0
0
votes
1
reply
1.2k
views
FilterVCF Filter '' failed: shape of 'skeleton' is not compatible with 'NROW(flesh)'
variantAnnotation
updated 4.6 years ago by 25k • written 4.6 years ago by • 0
2
votes
3
replies
1.5k
views
"Packages required but not available." rtracklayer in OSX is not available to CRAN, resulting in errors for downstream dependencies.
GenomicRanges rtracklayer VariantAnnotation S4Vectors SummarizedExperiment
updated 4.8 years ago by ★ 13k • written 4.8 years ago by ▴ 30
2
votes
3
replies
954
views
VariantAnnotation - subset multi-allele variants
variantAnnotation
updated 4.8 years ago by ★ 11k • written 4.8 years ago by • 0
0
votes
1
reply
779
views
negative AD value interfering with readVcfasVRanges
VariantAnnotation
updated 4.9 years ago by ★ 11k • written 4.9 years ago by • 0
0
votes
3
replies
1.0k
views
rbind VCF Two Objects Column Names Error
VariantAnnotation VCF
5.0 years ago Dario Strbenac ★ 1.5k
0
votes
0
replies
780
views
predictCoding warning message: serious or not?
software error annotation VariantAnnotation
updated 5.1 years ago by 3.9k • written 5.1 years ago by • 0
2
votes
3
replies
1.4k
views
Error in VCF parsing with VariantAnnotation
software error VariantAnnotation ensemblVEP
updated 5.2 years ago by ★ 6.8k • written 5.2 years ago by ▴ 20
0
votes
1
reply
946
views
VariantAnnotation fails to load VCF record
variantannotation
5.4 years ago Daniel Cameron ▴ 40
0
votes
6
replies
1.6k
views
How to prepare .vcf for seqCAT
seqCAT variantannotation gatk
updated 5.5 years ago by ▴ 30 • written 5.5 years ago by • 0
0
votes
1
reply
839
views
writeVcf save invalid vcf with metadata out of order
variantannotation
updated 5.5 years ago by ★ 6.8k • written 5.5 years ago by ▴ 20
1
vote
7
replies
3.1k
views
Data from ##SAMPLE lines in VCF?
variantannotation coldata
updated 5.6 years ago by ★ 6.8k • written 5.6 years ago by ▴ 10
3
votes
3
replies
1.3k
views
Get rs numbers using IntronVariants() in VariantAnnotation, locateVariants
variantannotation
updated 5.9 years ago by ★ 6.8k • written 5.9 years ago by ▴ 10
3
votes
4
replies
1.7k
views
Problem when transforming Platypus vcf to VRanges
variantannotation vcf readvcf vranges
updated 5.9 years ago by ★ 11k • written 5.9 years ago by • 0
0
votes
2
replies
1.2k
views
Error: invalid class "VRanges" object
variantannotation VRanges R Rle
updated 5.9 years ago by ★ 6.8k • written 5.9 years ago by • 0
0
votes
2
replies
1.2k
views
VariantAnnotation::locateVariants error coming from XVector
variantannotation xvector iranges
6.0 years ago Vivek.b ▴ 100
0
votes
2
replies
1.6k
views
filtering a VCF file based on genotype
variantannotation
updated 6.0 years ago by ★ 6.8k • written 6.0 years ago by ▴ 670
0
votes
1
reply
1.2k
views
VariantAnnotation and filtering a VCF
variantannotation
6.0 years ago Bogdan ▴ 670
50 results • Page 1 of 1
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Comment: Numerical differences in DESeq2 output depending on different design matrix cons by JKim • 0
The 1st model has an interaction term, but the 2nd model doesn't have the interaction term. That makes the difference.
Comment: Ensembl plants at annotationHub? by Daniele • 0
Hi, I'm using Ensembl Plants release 59 with the IWGSC RefSeq v1.1 gene annotation. Thanks a lot for replying so quickly!
Comment: Numerical differences in DESeq2 output depending on different design matrix cons by swbarnes2 ★ 1.4k
If you restrict yourself to, say, genes with a baseMean > 50, are the numerical differences between the two designs significant?
Comment: DESeq2- Mysterious interaction suppresses DEGs by shaunpeterson • 0
The images I tried to attach didn't attach. Here is the PCA (MDS) of all the samples, with the Cortex outlier highlighed. ![enter image de…
Comment: STRINGdb : error with string_db$plot_network() by damian.szk ▴ 80
ok. Forcing non-secure protocol should not be needed anymore, due to changes in the underlying library. However, I will look at why "HTTP" …
Votes
Answer: Error while installing BiocManager::install("org.Vdahliae.eg.db")
Comment: How can I create a eigencorplot of pca created from deseq2 object with PCAtools
Answer: Importing a GraphNEL into Cytoscape with RCy3 with error: "Error in cyrestPUT(pa
Answer: Importing a GraphNEL into Cytoscape with RCy3 with error: "Error in cyrestPUT(pa
Rsubread counting peaks ATACseq
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