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Comment:
C: Whole Genome Dna Amplification Before Applying Wgs
11.1 years ago by
Thomas
▴ 760
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0
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3.4k
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Comment:
C: Calling Of Rare Variant From The Illumina Human Exome Array
11.8 years ago by
Thomas
▴ 760
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0
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3.4k
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Comment:
C: Calling Of Rare Variant From The Illumina Human Exome Array
11.8 years ago by
Thomas
▴ 760
0
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0
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4.9k
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Comment:
C: User Friendly Tools For Genetic Association Studies
12.1 years ago by
Thomas
▴ 760
0
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0
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2.9k
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Comment:
C: Annovar And String Problems
12.3 years ago by
Thomas
▴ 760
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0
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8.7k
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Comment:
C: Conditional Analysis Of Snps (Ex From Gwas)
12.7 years ago by
Thomas
▴ 760
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0
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8.7k
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Comment:
C: Conditional Analysis Of Snps (Ex From Gwas)
12.7 years ago by
Thomas
▴ 760
1
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0
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3.8k
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Comment:
C: Identifying Snps Contributed By 1000Genomes Project
12.7 years ago by
Thomas
▴ 760
0
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0
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12k
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Comment:
C: Rare Variant Association Analysis
12.8 years ago by
Thomas
▴ 760
0
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0
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4.8k
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Comment:
C: Visualise Ld Plots On Whole Chromosome
12.8 years ago by
Thomas
▴ 760
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0
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4.8k
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Comment:
C: Visualise Ld Plots On Whole Chromosome
12.8 years ago by
Thomas
▴ 760
1
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4.8k
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Comment:
C: Visualise Ld Plots On Whole Chromosome
12.8 years ago by
Thomas
▴ 760
0
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0
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2.9k
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Comment:
C: Annovar And String Problems
12.8 years ago by
Thomas
▴ 760
0
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0
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7.9k
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Comment:
C: Tagsnps: Is There An Easy Way To Select Tagsnps From The 1000 Genomes Project?
12.8 years ago by
Thomas
▴ 760
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4.4k
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Comment:
C: Low-Coverage-Sequencing Combined With Array-Based Genotyping To Identify Allele-
13.0 years ago by
Thomas
▴ 760
0
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0
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4.4k
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Comment:
C: Low-Coverage-Sequencing Combined With Array-Based Genotyping To Identify Allele-
13.0 years ago by
Thomas
▴ 760
0
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4.3k
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Comment:
Comment: Deep Exome Sequencing And Alignment To Hg18 Or Hg19?
updated 3.0 years ago by
Ram
43k • written 13.0 years ago by
Thomas
▴ 760
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4.8k
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Comment:
C: Criteria For Calling Genotypes With High Certainty
13.1 years ago by
Thomas
▴ 760
0
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0
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4.8k
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Comment:
C: Criteria For Calling Genotypes With High Certainty
13.1 years ago by
Thomas
▴ 760
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