Showing: varscanreset
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Copy number variation detection
varscan copy number variation snp written 1 day ago by v2710 • updated 21 hours ago by d-cameron1.7k
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SNP/indel annotation in Arabidopsis
indel varscan arabidopsis snp written 4 weeks ago by Federico Giorgi370 • updated 4 weeks ago by finswimmer2.0k
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identifying TP53 germline mutations which are also in tumor cells.
somatic germline tp53 mutect varscan written 3 months ago by lait80 • updated 3 months ago by Noushin N520
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Work With Dnacopy (Bioconductor) And Varscan Copynumber Results
varscan bioconductor copynumber written 6.8 years ago by Mdeng510 • updated 5 months ago by 321bixin0
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varscan copy number error
varscan cnv written 5 months ago by mittu1602140
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Why CNV calling using VarScan need two steps of fragments merging?
varscan copy number variant cnv written 5 months ago by CY130 • updated 5 months ago by arta450
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Variant Calling in Low-Complexity Regions
indel low-complexity variants snp varscan written 7 months ago by ATpoint3.8k • updated 6 months ago by Biostar ♦♦ 20
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Running THetA2 with Varscan input?
varscan theta tumorpurity written 11 months ago by hshah20 • updated 7 months ago by j.p.albrecht30
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VarScan2 Parsing Error
varscan java written 8 months ago by ATpoint3.8k
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Tool: Varscan: Variant Detection In Massively Parallel Sequencing Data
indel varscan tool snp written 6.1 years ago by Istvan Albert ♦♦ 76k • updated 9 months ago by AcademicDialysis60
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SciClone on WES data
dnacopy varscan clonality wes sciclone written 12 months ago by mar.ark.parr30 • updated 11 months ago by Chris Miller19k
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varscan v2.3.9 filter Parse exception
varscan written 24 months ago by cafelumiere1270 • updated 12 months ago by jlx02480
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How to exclude noisy CNV from study?
dnacopy varscan copy number variation cnv wes written 14 months ago by rmateos.110 • updated 13 months ago by vchris_ngs4.5k
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Problems After Loading Varscan 2 Output Into Bioconductor.Dnacopy
exome varscan copynumber cnv sequencing written 5.2 years ago by sousuffer20 • updated 13 months ago by Biostar ♦♦ 20
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How to interpret tandem SNP in
varscan ngs dna-seq variants written 14 months ago by Paul1.1k
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varscan2 mpileup2snp output contains indels
vcf indels mpileup2snp varscan written 2.2 years ago by AW350 • updated 15 months ago by Biostar ♦♦ 20
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What allele frequency threshold do you recommend?
varscan written 17 months ago by agata88660 • updated 15 months ago by Biostar ♦♦ 20
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Exome-seq; Which tools to predict significantly muated genes .
varscan music cnv written 19 months ago by Chirag Nepal2.0k • updated 18 months ago by Biostar ♦♦ 20
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Gold Standard for Human cancer exome sequencing
somatic wes varscan mutect cancer written 18 months ago by Jerome Lin20 • updated 18 months ago by harold.smith.tarheel4.1k
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