Showing: snvreset
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3
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115
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Will random hexamer priming introduce SNP / SNV detection bias?
next-gen snv snp written 2 days ago by CY30 • updated 2 days ago by Pierre Lindenbaum96k
7
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1
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176
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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 11 days ago by Bogdan260 • updated 11 days ago by markus.riester180
1
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0
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226
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2
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1
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268
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1
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Defining LoF mutations with Annovar
annovar snv written 5 months ago by QVINTVS_FABIVS_MAXIMVS1.9k • updated 5 months ago by mforde84700
4
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0
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348
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Software to identify SNV and report mutation type
assembly sequence snv snp alignment written 9 months ago by Zar0 • updated 6 months ago by Biostar ♦♦ 20
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278
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0
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313
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local de novo assembly and split-read alignment at known sites and output bams?
indel snv written 8 months ago by lyz10302012260 • updated 8 months ago by Devon Ryan69k
4
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1
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564
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1
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1
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1
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559
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TCGA Broad Institute curated variants
broad institute tcga snv rna-seq written 15 months ago by umn_bist220 • updated 15 months ago by Istvan Albert ♦♦ 73k
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423
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2
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660
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Broad Institute TCGA MAF procedure
maf tcga snv rna-seq written 15 months ago by umn_bist220
4
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2
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627
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2
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Allele specific reads
allele specific reads snv atac-seq written 16 months ago by prasoon.agarwal10 • updated 16 months ago by Goutham Atla7.2k
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507
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543
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How to make column for the number of TCGA cases when doing SNV analysis?
gene tcga ccle snv cases written 19 months ago by agicict80 • updated 17 months ago by Biostar ♦♦ 20
2
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1
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638
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1
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Cosmic mutation signature
cosmic mutation signature snv written 18 months ago by agicict80 • updated 18 months ago by trausch630
0
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1
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543
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1
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About Dream Challenge Somatic Mutation Calling Algorithms
dream somatic mutations snv written 18 months ago by morovatunc360 • updated 18 months ago by TriS2.9k
8
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2
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613
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2
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Is it correct to merge TCGA mutation data from multiple centers
tcga snv written 18 months ago by vakul.mohanty230 • updated 18 months ago by Chris Miller18k
1
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1
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561
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1
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Can something like this be done in IGV or other better browsers
exome ggbio snv coverage written 22 months ago by Saad Khan310 • updated 22 months ago by Dan D6.0k
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678
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6
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2
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868
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databases of variants
api dbsnp snv written 2.3 years ago by Richard490 • updated 2.3 years ago by dandan330
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89
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39 follow
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0
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755
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1
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sciClone error for two sample
cna sciclone snv written 2.7 years ago by Lisa20 • updated 2.7 years ago by Chris Miller18k
2
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2
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867
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2
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determine potential SNVs and link them to phenotype
snv phenotype written 3.0 years ago by J.F.Jiang640 • updated 3.0 years ago by Kizuna700
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716
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True or False, SNVs using bwa+gatk
gatk snv bwa written 3.0 years ago by J.F.Jiang640
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