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<prev • 435 results • page 1 of 15 • next >
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Which softwares do you suggest to analysis CNV with Human660W-Quad_v1_H sap array?
660w snp array cnv human660w-quad_v1_h written 11 hours ago by Peter • 0
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Merge CNVnator output of multiple samples
wgs tool cnv written 23 hours ago by zhang248 • 20
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155
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Merging CNVs from multiple tumor samples from the same patient
multiple samples ngs facets cnv metastasis written 1 day ago by sey • 0 • updated 1 day ago by markus.riester • 190
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154
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Normalization of NGS data to make CNV calls
reads R ngs cnv normalization written 6 days ago by caspase8mach • 0
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detecting overlapping CNV from 2 algorithms
bedtools intersect r-gada penncnv cnv written 6 days ago by Myosotis1979 • 10
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calling the CNV in tumor-only samples (WGS and WES)
cnv written 12 days ago by Bogdan • 260
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16 follow
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Best Copy Number Variation Tools
cnv written 4.8 years ago by William • 3.9k • updated 11 days ago by Biostar ♦♦ 20
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129
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Gene list from copy number variation data
gene cnv written 13 days ago by akij • 50
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211
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WGS human normal panel
normal panel cnv written 14 days ago by benjaminnguyen90 • 0 • updated 14 days ago by Emily_Ensembl ♦ 12k
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Why copy number variations of TCGA is so high
genome tcga cnv written 19 days ago by akij • 50
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how to write for getting set of gene in one line having each sample name
R cnv written 20 days ago by raya.girish • 20 • updated 20 days ago by Pierre Lindenbaum ♦ 96k
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136
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Designing CNV analysis assay on Digital PCR
mitochondrial dna dpcr cnv written 28 days ago by dominik.saburo • 0
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159
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Copy number variation and its impact on allele frequency
maf cnv alle written 4 weeks ago by MAPK • 990
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118
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Difference of CN probes and SNP probes on genotyping microchip arrays
array affymetrix snp cnv written 4 weeks ago by Jimbou • 560 • updated 4 weeks ago by Biostar ♦♦ 20
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What is the importance of probe no and segmentation mean in Copy Number Variation data
cnv sequencing written 4 weeks ago by akij • 50
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141
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Error ecountered while running conifer with demo data set
python numpy conifer cnv written 5 weeks ago by mruduka.patel • 10 • updated 4 weeks ago by Rodrigo • 90
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345
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In FACETS, what does the mafR value represent?
cnv written 12 months ago by sviatoslav.kendall • 420 • updated 5 weeks ago by bruce.moran • 240
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6 follow
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WES or WGS analysis of cancer samples with no matched germline
wgs wes snv cnv written 5 weeks ago by Bogdan • 260 • updated 5 weeks ago by markus.riester • 190
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153
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1
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Detecting CNV can't cover aneuploidy situation
next-gen sequence cnv written 5 weeks ago by CY • 30 • updated 5 weeks ago by WouterDeCoster ♦ 20k
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1
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135
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1
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Is there any tool can identify which copy of chromosome reads coming from?
alignment cnv sequencing written 5 weeks ago by qyang • 20 • updated 5 weeks ago by Brian Bushnell ♦ 13k
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1
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157
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1
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CNVkit GRCh38 tumor-normal pair
wes tcga grch38 cnv bed written 5 weeks ago by plink_9857 • 40 • updated 5 weeks ago by Eric T. • 1.8k
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5 follow
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CNV detection of single cell genome sequencing
cnvkit single cell genome sequencing cnv written 5 weeks ago by Tonny • 10 • updated 5 weeks ago by Eric T. • 1.8k
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Annotation for SV and CNV
sv annotation cnv written 14 months ago by always_learning • 780 • updated 6 weeks ago by fjpt.com • 0
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1
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173
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1
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CNVnator Compile issue
sv ngs cnvnator cnv written 6 weeks ago by gessthomsxavier7 • 10
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1
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158
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1
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Should unplaced scaffolds in reference genome be used to map newly sequenced genome
unplaced scaffolds reference based assembly cnv written 11 weeks ago by chevivien • 60 • updated 6 weeks ago by Vijay Lakhujani • 1.1k
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CNV tool for small sequences
tool cnv coverage written 7 weeks ago by jsgounot • 130 • updated 7 weeks ago by bdelolmo • 10
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246
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1
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Using cnvkit for targeted amplicon sequencing
cnvkit targeted amplicon sequencing reference cnv written 9 weeks ago by ingrid.schulman • 0 • updated 7 weeks ago by Eric T. • 1.8k
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193
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What is probe number and segmentation mean in copy number variation(CNV) data
probe cnv written 8 weeks ago by akij • 50 • updated 7 weeks ago by Eric T. • 1.8k
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151
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CNVkit - creating a reference panel from 'normal' parts of tumour bams
cnvkit sequencing cnv tumour written 7 weeks ago by ferenju • 0
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How generate mappbility and gcWinds files from Bam files of non human genome
genome cnv written 11 weeks ago by misbahabas • 30 • updated 8 weeks ago by Biostar ♦♦ 20
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