Showing: snpreset
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13
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Pfb File For Cnv Analysis Using Illumina 610 Quad V1 Arrays
illumina bioconductor cnv snp written 8.2 years ago by Neilfws48k • updated 8 days ago by Ram17k
5
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2
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Annovar result explanation
annotation next-gen snp annovar written 13 months ago by anu014150 • updated 9 days ago by tannerkoomar20
4
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1
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138
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1
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How to retrieve Gene name from SNP ID using biomaRt
gene R biomart rsid snp written 11 days ago by johnS0 • updated 11 days ago by Kevin Blighe28k
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3
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How to add custom fields to the VCF files?
vcf annotation phasing snp manipulation written 2.1 years ago by kirannbishwa01850 • updated 11 days ago by sm.hashemin60
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How To Detect And Query Poly-Allelic Snps?
biomart allele dbsnp snp written 8.5 years ago by Michael Dondrup44k • updated 12 days ago by Ram17k
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SNP filtering from specific regions
snp written 12 days ago by ashaneev070
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what is the conventional apporach to calculate depth of coverage?
wgs dnaseq coverage snp depth written 12 days ago by serpalma.v10 • updated 12 days ago by finswimmer5.3k
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Association Analysis with Plink error
plink2 association plink snp written 2.5 years ago by mmukhame32130 • updated 12 days ago by zx87544.9k
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estimate dN/dS ratio for multiple genes
snp written 8 weeks ago by paraskevopou10 • updated 12 days ago by Biostar ♦♦ 20
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5
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177
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6 follow
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how to count variants par sample per chromosome in a vcf file?
snp written 13 days ago by nagarsaggi0 • updated 13 days ago by chrchang5233.9k
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0
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109
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Adjusting SNP frequency
snp written 13 days ago by anthony.nash0
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1
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149
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1
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PRSice: Imputation and clumping
prsice gwas polygenic risk score snp written 5 weeks ago by muraved0 • updated 13 days ago by Sam2.1k
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3
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83
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Cross validation error Admixture
software error snp written 3.5 years ago by benhalimayossra0 • updated 14 days ago by Biostar ♦♦ 20
2
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1
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129
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5 follow
1
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Handling manhattan plots in vector graphics editors
R snp written 14 days ago by yury.barbitoff20 • updated 14 days ago by Pierre Lindenbaum112k
3
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1
answer
94
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1
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Flanking sequences around cancer variants
genome cancer_variants snp written 14 days ago by banerjeeshayantan70 • updated 14 days ago by jared.andrews071.2k
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GISTIC input parameters.
gistic snp cnv written 14 days ago by rin20 • updated 14 days ago by EagleEye5.6k
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5
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How to identify Homozygous or Heterozygous variants from the annotation file ?
next-gen snp written 3.3 years ago by deepue110 • updated 14 days ago by Kevin Blighe28k
1
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1
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107
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1
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Cox Regression and Linkage Disequilibrium
R cox survival snp linkage disequilbrium written 16 days ago by krc30040 • updated 15 days ago by Kevin Blighe28k
12
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257
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7 follow
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what is the difference between polymorphism and mutation and variant?
gene genome snp written 16 days ago by nabiyari10 • updated 15 days ago by Michael Dondrup44k
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827
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VCF file period symbol in the genotype
vcf variant snp written 18 months ago by bharata1803290 • updated 15 days ago by Ram17k
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