Showing: snvreset
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Dataset preparation for driver/passenger gene discovery
gene tcga snv snp cancer written 9 weeks ago by mhasa00620 • updated 9 weeks ago by Kevin Blighe7.2k
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Tool to identify recurrent mutations directly from VCF
vcf recurrent mutation mutation snv written 10 weeks ago by ATPoint2.4k • updated 10 weeks ago by jared.andrews07290
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determine loss- or gain-of-function of specific mutation
mutation variant snv written 3 months ago by igor4.7k • updated 3 months ago by mforde841000
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Transcriptional strand bias on SNV from exome data
exome strand-bias snv written 3 months ago by Chirag Nepal1.9k • updated 3 months ago by Biostar ♦♦ 20
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Will random hexamer priming introduce SNP / SNV detection bias?
next-gen snv snp written 4 months ago by CY40 • updated 4 months ago by Pierre Lindenbaum101k
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WES or WGS analysis of cancer samples with no matched germline
wgs wes snv cnv written 4 months ago by Bogdan300 • updated 4 months ago by markus.riester210
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Defining LoF mutations with Annovar
annovar snv written 9 months ago by QVINTVS_FABIVS_MAXIMVS2.0k • updated 9 months ago by mforde841000
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Software to identify SNV and report mutation type
assembly sequence snv snp alignment written 13 months ago by Zar0 • updated 10 months ago by Biostar ♦♦ 20
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local de novo assembly and split-read alignment at known sites and output bams?
indel snv written 12 months ago by lyz10302012260 • updated 12 months ago by Devon Ryan73k
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TCGA Broad Institute curated variants
broad institute tcga snv rna-seq written 19 months ago by umn_bist260 • updated 18 months ago by Istvan Albert ♦♦ 74k
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Broad Institute TCGA MAF procedure
maf tcga snv rna-seq written 19 months ago by umn_bist260
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Allele specific reads
allele specific reads snv atac-seq written 20 months ago by prasoon.agarwal10 • updated 20 months ago by geek_y8.1k
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How to make column for the number of TCGA cases when doing SNV analysis?
gene tcga ccle snv cases written 23 months ago by agicict110 • updated 21 months ago by Biostar ♦♦ 20
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Cosmic mutation signature
cosmic mutation signature snv written 22 months ago by agicict110 • updated 22 months ago by trausch760
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About Dream Challenge Somatic Mutation Calling Algorithms
dream somatic mutations snv written 22 months ago by morovatunc360 • updated 22 months ago by TriS3.1k
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Is it correct to merge TCGA mutation data from multiple centers
tcga snv written 22 months ago by vakul.mohanty230 • updated 22 months ago by Chris Miller19k
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Can something like this be done in IGV or other better browsers
exome ggbio snv coverage written 2.2 years ago by Saad Khan310 • updated 2.2 years ago by Dan D6.2k
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databases of variants
api dbsnp snv written 2.6 years ago by Richard500 • updated 2.6 years ago by dandan330
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