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cnv
•
reset
1
vote
2
replies
1.4k
views
Difficulty dowloading hg38 cnv data in tcgabiolinks
TCGAbiolinks
cnv
3.2 years ago • updated 3.1 years ago
raf4
▴ 30
7
votes
9
replies
2.0k
views
QSEA : Internal CNV analysis and cancer type-specific TCGA 450K Human Methylation Calibration Dataset
MEDIP-seq
CNV
TCGA450KHumanMethylationCalibrationDataset
qsea
PRAD
3.6 years ago
rtrivedi1
▴ 10
0
votes
0
replies
708
views
Applying exomeCopy to call CNVs withouts controls considering batch effects
exomeCopy
CNV
WES
3.7 years ago
Cheng
• 0
4
votes
13
replies
3.9k
views
Gaia not returning results - load_cnv problem
gaia
cnv
updated 3.3 years ago by
juanmafernandezm86
• 0 • written 6.4 years ago by
rina
▴ 30
2
votes
4
replies
1.1k
views
CopywriteR job runs out of memory
copywriter
cnv
updated 4.7 years ago by
oscarkrijgsman
▴ 20 • written 4.7 years ago by
Ram
▴ 220
0
votes
1
reply
861
views
How to use panelcn.mops to detect CNVs from whole genome data by getting count windows from BED file?
cn.mops
panelcn.mops
CNV detection
CNV
4.8 years ago
metzgerlukas
• 0
0
votes
0
replies
615
views
cn.mops : undef chromsome using data matrix as input
CNV
cn.mops
undef
4.8 years ago
ankita.narang86
• 0
0
votes
0
replies
888
views
cn.MOPS output - mean/median of what?
cn.MOPS
CNV
copy number
4.9 years ago
liorglic
▴ 10
0
votes
1
reply
979
views
PureCN: Why is average coverage used for segmentation and not the denoised fragment counts?
PureCN
CNV
CNA
segmentation
calculateTangentNormal
updated 5.0 years ago by
markus.riester
▴ 130 • written 5.0 years ago by
sruddy17
• 0
0
votes
1
reply
932
views
CNV plot using cn.mops
cnv
R
plot visualization
cn.mops
software error
5.0 years ago
ari
• 0
0
votes
0
replies
746
views
ExomeDepth package- error with "select.reference.set" function
ExomeDepth
CNV
5.0 years ago
Bouzid.a
▴ 20
0
votes
1
reply
1.0k
views
Error using singlecn.mops for cnv detection in WGS data
cnv
cn.mops
singlecn.mops
updated 2.8 years ago by
SicilianSilicon
• 0 • written 5.1 years ago by
frez111
• 0
0
votes
2
replies
1.4k
views
CNV in Normal Samples?
PureCN
Germline
Normal
CNV
updated 6.3 years ago by
markus.riester
▴ 130 • written 6.3 years ago by
twtoal
▴ 10
0
votes
2
replies
2.9k
views
Error: vector memory exhausted (limit reached?)
tcgabiolinks
tcga
cnv
mac os x
gaia
updated 6.4 years ago by
rreck
▴ 20 • written 6.4 years ago by
rina
▴ 30
2
votes
3
replies
1.7k
views
Doubt about WL in cn.mops
dnacopy
dnaseq
genomic
cn.mops
cnv
updated 6.5 years ago by
Günter Klambauer
▴ 540 • written 6.5 years ago by
Cased
• 0
0
votes
0
replies
1.1k
views
Noise Analyses of CNV Data from TCGA
tcgabiolinks
tcga
cnv
noise
pruning
6.5 years ago
jrlarsen
▴ 10
0
votes
4
replies
1.4k
views
Does Greater Depth Allow Low Purity To Work Well?
PureCN
Purity
Low Purity
CNV
6.6 years ago
twtoal
▴ 10
3
votes
2
replies
1.1k
views
counting the sequencing reads in 10kb regions on a genome-wide scale
read counting
CNV
rsamtools
updated 6.8 years ago by
James W. MacDonald
67k • written 6.8 years ago by
Bogdan
▴ 670
0
votes
0
replies
1.2k
views
how to analyze "Beta-score" and get CNVdata using Comunee
conumee
CNV
450K
6.9 years ago
bird.of.clockwise
• 0
0
votes
0
replies
969
views
visualize CNV data based on WGS
CNV
7.0 years ago
Bogdan
▴ 670
0
votes
3
replies
1.2k
views
exomeCopy error with compileCopyCountSegments
exomecopy
cnv
7.0 years ago
ramakrishnas
• 0
0
votes
2
replies
1.7k
views
cn.MOPs issue with "Error in if (all(segMedianT == 0))"
cn.mops
cnv
updated 7.0 years ago by
Günter Klambauer
▴ 540 • written 7.0 years ago by
martyferr90
▴ 20
2
votes
2
replies
1.6k
views
detecting of CNV in WGS/WES data
CNV
WGS
WES
updated 7.4 years ago by
Haiying.Kong
▴ 110 • written 7.5 years ago by
Bogdan
▴ 670
0
votes
2
replies
1.1k
views
Filter CNVs if contain certain gene
cnv
genomic ranges
cnvs
7.5 years ago
julrodr80
▴ 30
2
votes
2
replies
1.2k
views
list fo genes by cnv
cnv
genes
genomic ranges
splitByOverlap
updated 7.7 years ago by
Martin Morgan
25k • written 7.7 years ago by
julrodr80
▴ 30
0
votes
0
replies
1.4k
views
DNA methylation 450k data - minfi - preprocessFunnorm - CNV cases vs non-CNV controls
CNV
minfi
preprocessing
dna methylation
7.8 years ago
Thomas
• 0
4
votes
9
replies
2.7k
views
How to use cn.mops to detect CNVs from Targeted DNA Sequencing data?
cn.mops
cnv
targeted sequencing
updated 8.0 years ago by
Günter Klambauer
▴ 540 • written 8.0 years ago by
Bouzid.a
▴ 20
0
votes
4
replies
1.5k
views
CNV caller software
CNV
8.3 years ago
Bogdan
▴ 670
0
votes
1
reply
1.1k
views
Union of GenomicRanges problem when one range is empty
genomicranges
R
cnv
8.4 years ago
WouterDeCoster
▴ 130
0
votes
0
replies
1.4k
views
crlmm: Does it support Illumina BeadChip platform HumanCore-24v1-0_A
cnv
cnvtools
crlmm
8.4 years ago
enriquev
• 0
0
votes
1
reply
1.8k
views
CopywriteR: CNV calling on normals samples / gaps in chromosomes
copynumber
cnvtools
cnv
copywriteR
updated 8.4 years ago by
t.kuilman
▴ 170 • written 8.4 years ago by
ahinsahr11
• 0
0
votes
1
reply
1.7k
views
ExomeDepth Package Error Messages
cnv
exome
8.8 years ago
Bio152
▴ 150
1
vote
5
replies
1.8k
views
Is there any way of exporting CNV data from Affymetrix SNP 6.0 arrays from Nexus Software for OncoScan?
cnv
nexus for oncoscan
Affymetrix 6.0
.BGR
8.9 years ago
IOM
▴ 20
1
vote
4
replies
1.8k
views
Detect CNVs in target sample
CNV
cn.mops
updated 9.0 years ago by
Günter Klambauer
▴ 540 • written 9.0 years ago by
ashkot09
• 0
2
votes
6
replies
2.0k
views
refSeqName issue in cn.MOPS
CNV
cn.mops
updated 9.0 years ago by
Günter Klambauer
▴ 540 • written 9.0 years ago by
ashkot09
• 0
0
votes
1
reply
1.4k
views
exomeCopy copy number setting
cnv
exomecopy
updated 9.1 years ago by
Michael Love
43k • written 9.1 years ago by
cafelumiere12
▴ 20
1
vote
3
replies
1.5k
views
Error: could not find function "readGVF"
GVF
CNV
cnvGSA
updated 9.2 years ago by
James W. MacDonald
67k • written 9.2 years ago by
Vinicius Henrique da Silva
▴ 40
0
votes
1
reply
1.3k
views
NGScopy package throwing error during installation
NGScopy
installation
CNV
9.4 years ago
JstRoRR
• 0
2
votes
2
replies
1.9k
views
Adjusting the defaults in the cn.MOPs Package
cn.mops
cnv
cnvtools
updated 9.5 years ago by
Günter Klambauer
▴ 540 • written 9.5 years ago by
voksdvoks
• 0
2
votes
8
replies
2.7k
views
Copy Number Variation in the cn.mops Package
cn.mops
cnv
cnvtools
updated 9.5 years ago by
Martin Morgan
25k • written 9.5 years ago by
bioconductor
• 0
0
votes
0
replies
1.4k
views
'GenomeInfoDb' error in the cn.MOPS Package
cnv
genomeinfodb
9.5 years ago
voksdvoks
• 0
0
votes
3
replies
1.7k
views
Mapping of two different regions to one gene symbol
TCGA
CNV
updated 9.6 years ago by
Marc Carlson
★ 7.2k • written 9.6 years ago by
NS
▴ 60
0
votes
4
replies
1.6k
views
Trouble following the first 5 lines of vanillaICE tutorial?
SNP6
crlmm
vanillaice
vanillaice crlmm
cnv
updated 9.6 years ago by
rscharpf
• 0 • written 9.6 years ago by
cafelumiere12
▴ 20
0
votes
2
replies
3.5k
views
Pipeline for analyzing CNV (SNP array) level 3 from TCGA
SNP
CNV
TCGA
9.7 years ago
NS
▴ 60
0
votes
0
replies
1.5k
views
DNAcopy default settings and SNP6.0 arrays
SNP
DNAcopy
SNP6.0
CNV
9.9 years ago
giovanni.dario
• 0
45 results • Page
1 of 1
Recent ...
Replies
Comment: Any tools to convert .gff to .gtf format
by
ControlF5
• 0
Yes, the Appsierra team recently built a tool to convert .gff to .gtf format. [ControlF5][1] is providing the best software testing service…
Comment: EuroBioC2024 abstract submission is open!
by
Alan Downey
• 0
EuroBioC2024 has opened its abstract submission process, presenting an exciting opportunity for researchers to contribute to groundbreaking…
Comment: ChAMP.DMR error - Error in makeGenomicRatioSetFromMatrix
by
O'Brien
• 0
Consult the ChAMP.DMR documentation for more information on supported array types and expected data formats: https://bioconductor.org/packa…
Answer: combining raw counts and estimated counts
by
O'Brien
• 0
It is possible to combine raw counts from TCGA and estimated counts from GEO datasets (Kalisto pseudoalignment) while mitigating batch effe…
Comment: Packages don't update, but no error or warning is thrown
by
neighsanlo
• 0
@[sandtrix][1] This is useful information. [1]: https://sandtrix.io
Votes
A: GWAS analysis with Illumina HumanOmni5-4 BeadChip - recommended software and wor
A: GWAS analysis with Illumina HumanOmni5-4 BeadChip - recommended software and wor
A: RNA-seq Normalisation - normalise all samples in experiment or only the ones use
Answer: Can DESeq2's design compensate for sequencing experimental design shortcomings?
Comment: Issues with seqlevelsStyle when making custom txdb objects for genomes/annotatio
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