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Genomestrip 2.0 CNV pipeline
CNV genomestrip SGE
7.3 years ago by willgilks ▴ 360
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4.0k
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Answer: A: Genomestrip 2.0 CNV pipeline
7.3 years ago by willgilks ▴ 360
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3.2k
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Window and step size for LD-independent SNPs
r2 ld plink SNP snp
7.8 years ago by willgilks ▴ 360
6
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1
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16k
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Answer: A: Subsetting individuals with Plink. Error: Line 1 of --keep file has fewer tokens
7.9 years ago by willgilks ▴ 360
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3.4k
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Answer: A: Load BED file on UCSC
8.1 years ago by willgilks ▴ 360
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3.8k
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Answer: A: Best visual and interactive genotype matrix (VCF) exploration tool
8.1 years ago by willgilks ▴ 360
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2.5k
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Answer: A: Genetic measures calculation in vcf files
8.1 years ago by willgilks ▴ 360
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4.5k
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Answer: A: How to conduct pathway analysis from VCF file?
8.1 years ago by willgilks ▴ 360
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8.9k
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Answer: A: How to overlay qq plots
8.1 years ago by willgilks ▴ 360
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4.5k
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Answer: A: How to conduct pathway analysis from VCF file?
8.1 years ago by willgilks ▴ 360
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3.3k
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Answer: A: How to predict amino acid sequence after a framshift deletion in the gene
8.1 years ago by willgilks ▴ 360
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1
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2.1k
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Answer: A: Problems with converting data
8.1 years ago by willgilks ▴ 360
2
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1
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3.9k
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Answer: A: which R package to use to do Quality control for SNPs data
8.1 years ago by willgilks ▴ 360
2
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0
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3.7k
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Answer: A: GWAS analysis on PLINK
8.1 years ago by willgilks ▴ 360
2
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1
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4.5k
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Answer: A: Linkage disequilibrium decay sanity check
8.1 years ago by willgilks ▴ 360
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3.2k
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Answer: A: Filreing vcf files not giving any results
8.1 years ago by willgilks ▴ 360
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5.4k
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Answer: A: Replace vcf in-house variant IDs with dnSNP variant IDs
8.1 years ago by willgilks ▴ 360
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1
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3.2k
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Answer: A: How to rotate dotchart for gene expression profile?
8.1 years ago by willgilks ▴ 360
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1
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3.2k
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Answer: A: Filreing vcf files not giving any results
8.1 years ago by willgilks ▴ 360
6
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6
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5.4k
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Replace vcf in-house variant IDs with dnSNP variant IDs
vcf SNP genome next-gen-sequencing
updated 2.6 years ago by 45k • written 9.5 years ago by ▴ 360
5
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4.0k
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Answer: A: Box plot using ggplot2
8.2 years ago by willgilks ▴ 360
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1
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5.4k
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Comment: A: Replace vcf in-house variant IDs with dnSNP variant IDs
8.2 years ago by willgilks ▴ 360
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2.5k
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Answer: A: Format VCF for dbSNP upload
8.2 years ago by willgilks ▴ 360
2
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1
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2.5k
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Format VCF for dbSNP upload
formatting vcf gatk dbSNP SNPeff
updated 2.6 years ago by 45k • written 9.4 years ago by ▴ 360
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7.2k
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Answer: A: Genotype And Snp Calling Review Papers
8.2 years ago by willgilks ▴ 360
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1.8k
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Answer: A: Infer CNVs from SNP variant allele fractions
8.2 years ago by willgilks ▴ 360
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1
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2.6k
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Answer: A: aneuploidy detection in DNA sequencing
8.2 years ago by willgilks ▴ 360
4
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53k
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Answer: A: Convert plink files to VCF: Reference allele file
8.6 years ago by willgilks ▴ 360
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1.9k
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Answer: A: Genomestrip Generate Haploid CNV Genotypes
8.9 years ago by willgilks ▴ 360
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1
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1.9k
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Genomestrip Generate Haploid CNV Genotypes
cnv genomestrip generatehaploidcnvgenotypes
8.9 years ago by willgilks ▴ 360
2
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2.6k
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Answer: A: heatmap in R software or any software
9.0 years ago by willgilks ▴ 360
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4.9k
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Answer: Answer: GWAS dataset: SNPs with association p-value
updated 3.0 years ago by 45k • written 10.2 years ago by ▴ 360
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