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questions
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963
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Complete variant toolbox: gmapR/VariantTools/VariantAnnotation - revived
VariantAnnotation
Annotation
GenomicRanges
VariantAnnotation
GenomicAlignments
Annotation
9.8 years ago
Valerie Obenchain
★ 6.8k
0
votes
5
replies
1.2k
views
Complete variant toolbox: gmapR/VariantTools/VariantAnnotation - revived
VariantAnnotation
GenomicRanges
VariantAnnotation
VariantAnnotation
GenomicRanges
updated 9.8 years ago by
Robert Castelo
★ 3.3k • written 9.8 years ago by
Valerie Obenchain
★ 6.8k
0
votes
10
replies
2.8k
views
GenomicAlignments - Speeding up readGAlignmentPairs()
Cancer
RNAseqData
GenomicFeatures
Cancer
RNAseqData
GenomicFeatures
updated 9.9 years ago by
Fong Chun Chan
▴ 320 • written 9.9 years ago by
Valerie Obenchain
★ 6.8k
0
votes
0
replies
552
views
Bioconductor newsletter - July 2014
Cancer
Cancer
9.9 years ago
Valerie Obenchain
★ 6.8k
0
votes
4
replies
1.5k
views
GenomicAlignments and QNAME collision
RNASeq
Cancer
convert
Rsamtools
GenomicAlignments
RNASeq
Cancer
convert
Rsamtools
updated 9.9 years ago by
Stefano Calza
▴ 90 • written 9.9 years ago by
Valerie Obenchain
★ 6.8k
0
votes
2
replies
687
views
Bioconductor newsletter: April 2014
Cancer
Cancer
updated 10.1 years ago by
Malcolm Cook
★ 1.6k • written 10.1 years ago by
Valerie Obenchain
★ 6.8k
0
votes
0
replies
1.1k
views
ensemblVEP, variant_effect_predictor versions and release schedule
Cancer
MLInterfaces
bridge
ensemblVEP
AnnotationHub
Cancer
MLInterfaces
bridge
ensemblVEP
10.4 years ago
Valerie Obenchain
★ 6.8k
0
votes
0
replies
1.3k
views
zero-row result breaks select() on PolyPhen.Hsapiens.* and SIFT.Hsapiens.*
VariantAnnotation
Annotation
PolyPhen
SIFT
annotate
VariantAnnotation
ensemblVEP
Annotation
10.5 years ago
Valerie Obenchain
★ 6.8k
0
votes
2
replies
1.1k
views
readVcf fails when ALT field contains breakends and no symbolic allele
VariantAnnotation
VariantAnnotation
VariantAnnotation
VariantAnnotation
updated 10.5 years ago by
Daniel Cameron
▴ 40 • written 10.5 years ago by
Valerie Obenchain
★ 6.8k
0
votes
1
reply
834
views
stranded intronic variants with VariantAnnotation::locateVariants()
Annotation
Annotation
updated 10.5 years ago by
Robert Castelo
★ 3.3k • written 10.5 years ago by
Valerie Obenchain
★ 6.8k
0
votes
0
replies
695
views
VariantAnnotation: Specifying 'seqinfo' at import with 'readVcf'
GenomicRanges
GenomicRanges
10.6 years ago
Valerie Obenchain
★ 6.8k
0
votes
2
replies
848
views
using a gtf file to map reads
GO
GenomicFeatures
DEXSeq
GO
GenomicFeatures
DEXSeq
updated 10.9 years ago by
Alejandro Reyes
★ 1.9k • written 10.9 years ago by
Valerie Obenchain
★ 6.8k
0
votes
0
replies
453
views
summarizeOverlaps: ambiguous method dispatch
GO
GO
10.9 years ago
Valerie Obenchain
★ 6.8k
0
votes
0
replies
978
views
[devteam-bioc] sort error in GRange
rtracklayer
GenomicRanges
rtracklayer
GenomicRanges
11.0 years ago
Valerie Obenchain
★ 6.8k
0
votes
1
reply
1.2k
views
summarizeOverlaps mode ignoring inter feature overlaps
GenomicRanges
Rsamtools
GenomicRanges
Rsamtools
updated 11.0 years ago by
Thomas Girke
★ 1.7k • written 11.0 years ago by
Valerie Obenchain
★ 6.8k
0
votes
0
replies
1.0k
views
Subsetting vcf file by subject
VariantAnnotation
Annotation
cycle
VariantAnnotation
VariantAnnotation
Annotation
cycle
11.1 years ago
Valerie Obenchain
★ 6.8k
1
vote
4
replies
5.6k
views
merging VCF files
VariantAnnotation
VariantAnnotation
VariantAnnotation
VariantAnnotation
written 11.3 years ago by
Valerie Obenchain
★ 6.8k
0
votes
0
replies
415
views
ExpressionSet Object
11.2 years ago
Valerie Obenchain
★ 6.8k
0
votes
1
reply
599
views
Why does a call to "unique" removes a DNAStringSet names?
updated 11.5 years ago by
Hervé Pagès
16k • written 11.5 years ago by
Valerie Obenchain
★ 6.8k
0
votes
0
replies
1.4k
views
Rle factors, table and empty levels
IRanges
IRanges
11.5 years ago
Valerie Obenchain
★ 6.8k
0
votes
1
reply
2.5k
views
Integer overflow when summing an 'integer' Rle
Coverage
GO
Cancer
convert
IRanges
Coverage
GO
Cancer
convert
IRanges
updated 11.7 years ago by
delhomme@embl.de
★ 1.2k • written 11.7 years ago by
Valerie Obenchain
★ 6.8k
0
votes
0
replies
1.4k
views
GenomicRanges: nearest() for GRanges not returning overlaps
IRanges
GenomicRanges
IRanges
GenomicRanges
11.7 years ago
Valerie Obenchain
★ 6.8k
0
votes
0
replies
722
views
Bioc2012 : July 24-25
Microarray
Microarray
11.9 years ago
Valerie Obenchain
★ 6.8k
0
votes
0
replies
519
views
BioC2012 deadlines
11.9 years ago
Valerie Obenchain
★ 6.8k
0
votes
0
replies
725
views
BioC 2012
12.0 years ago
Valerie Obenchain
★ 6.8k
0
votes
1
reply
922
views
Finding coding SNPs with predictCoding
SNP
Annotation
BSgenome
BSgenome
GenomicFeatures
cycle
genomes
SNP
Annotation
BSgenome
updated 12.0 years ago by
Thomas Girke
★ 1.7k • written 12.0 years ago by
Valerie Obenchain
★ 6.8k
0
votes
1
reply
1.1k
views
Question regarding COA plot generated by made4 package
made4
made4
updated 12.0 years ago by
Aedin Culhane
▴ 510 • written 12.0 years ago by
Valerie Obenchain
★ 6.8k
0
votes
7
replies
1.2k
views
distanceToNearest for GRanges?
Cancer
GenomicRanges
Cancer
GenomicRanges
updated 12.1 years ago by
Michael Muratet
▴ 420 • written 12.1 years ago by
Valerie Obenchain
★ 6.8k
0
votes
2
replies
1.2k
views
Finding coding SNPs with predictCoding
SNP
Annotation
BSgenome
ctc
BSgenome
cycle
genomes
SNP
Annotation
BSgenome
ctc
BSgenome
updated 12.1 years ago by
Thomas Girke
★ 1.7k • written 12.1 years ago by
Valerie Obenchain
★ 6.8k
0
votes
5
replies
1.4k
views
Finding coding SNPs with predictCoding
SNP
ctc
SNP
ctc
updated 12.2 years ago by
Thomas Girke
★ 1.7k • written 12.2 years ago by
Valerie Obenchain
★ 6.8k
0
votes
1
reply
796
views
countOverlaps within Mode Counting
Cancer
Cancer
updated 12.2 years ago by
Dario Strbenac
★ 1.5k • written 12.2 years ago by
Valerie Obenchain
★ 6.8k
0
votes
2
replies
1.2k
views
Help With RNA-seq
Annotation
Normalization
Kidney
edgeR
baySeq
Annotation
Normalization
Kidney
edgeR
baySeq
12.3 years ago
Valerie Obenchain
★ 6.8k
0
votes
0
replies
1.2k
views
[Rocky] - R code for PGSEA package to identify differentially expressed genes
GO
affy
limma
GLAD
PGSEA
GSEABase
GO
affy
limma
GLAD
PGSEA
GSEABase
12.3 years ago
Valerie Obenchain
★ 6.8k
0
votes
3
replies
2.4k
views
How to prepare Custom INPUT(DATA) files for GAGE Analysis and DO a BASIC GAGE analysis using those files
Microarray
GO
Cancer
Breast
gage
Microarray
GO
Cancer
Breast
gage
updated 12.3 years ago by
Javerjung Sandhu
▴ 200 • written 12.3 years ago by
Valerie Obenchain
★ 6.8k
0
votes
0
replies
800
views
countGenomicOverlaps output
GenomicRanges
GenomicRanges
12.6 years ago
Valerie Obenchain
★ 6.8k
0
votes
0
replies
953
views
rsamtools scanBcf segfault
VariantAnnotation
Rsamtools
VariantAnnotation
VariantAnnotation
Rsamtools
VariantAnnotation
12.7 years ago
Valerie Obenchain
★ 6.8k
0
votes
0
replies
1.1k
views
PGSEA and smcPlot
GO
hgu133plus2
PGSEA
GO
hgu133plus2
PGSEA
12.8 years ago
Valerie Obenchain
★ 6.8k
0
votes
0
replies
462
views
BioC2011 - lab preparation
12.8 years ago
Valerie Obenchain
★ 6.8k
0
votes
0
replies
597
views
BioC2011 - lab sign up
12.8 years ago
Valerie Obenchain
★ 6.8k
0
votes
0
replies
661
views
BioC2011 - registration reminder
12.9 years ago
Valerie Obenchain
★ 6.8k
0
votes
1
reply
1.9k
views
maSigPro and "subscript out of bounds"
Normalization
Regression
maSigPro
Normalization
Regression
maSigPro
updated 12.9 years ago by
Andrea Grilli
▴ 240 • written 12.9 years ago by
Valerie Obenchain
★ 6.8k
0
votes
0
replies
596
views
call for BioC2011 posters
13.0 years ago
Valerie Obenchain
★ 6.8k
0
votes
0
replies
1.2k
views
[maSigPro] Splitting data - how?
maSigPro
maSigPro
13.0 years ago
Valerie Obenchain
★ 6.8k
0
votes
0
replies
1.0k
views
Bioconductor
cdf
affy
affyPara
cdf
affy
affyPara
13.6 years ago
Valerie Obenchain
★ 6.8k
44 results • Page
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