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Comment: Comment: Allele frequency for genes
2.6 years ago by German.M.Demidov ★ 2.9k
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Comment: Comment: Allele frequency for genes
2.6 years ago by German.M.Demidov ★ 2.9k
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4.0k
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Comment: Comment: How to estimate polygenic risk score (PRSs) using the scoring files from PGSCata
2.6 years ago by German.M.Demidov ★ 2.9k
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821
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Comment: Comment: Variant Allele Frequency
2.6 years ago by German.M.Demidov ★ 2.9k
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562
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Comment: Comment: How is better perform the analyze the somatic mutations? (the mutations of my in
2.6 years ago by German.M.Demidov ★ 2.9k
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1.3k
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Comment: Comment: Rare variant association analysis (SKAT-O) - Power calculation
2.7 years ago by German.M.Demidov ★ 2.9k
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1
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1.3k
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Comment: Comment: Rare variant association analysis (SKAT-O) - Power calculation
2.7 years ago by German.M.Demidov ★ 2.9k
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0
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839
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Comment: Comment: Germline Cancer Mutations
2.7 years ago by German.M.Demidov ★ 2.9k
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1
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3.1k
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Comment: Comment: Dealing with P value inflation of SNPs identified by qqplot
2.7 years ago by German.M.Demidov ★ 2.9k
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1
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721
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Comment: Comment: Regarding p53 (tumour suppressor gene) mutation and overexpression relation with
2.7 years ago by German.M.Demidov ★ 2.9k
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1
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3.1k
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Comment: Comment: Dealing with P value inflation of SNPs identified by qqplot
2.7 years ago by German.M.Demidov ★ 2.9k
0
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1
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2.0k
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Comment: Comment: Dante vs Nebula indexcov
2.7 years ago by German.M.Demidov ★ 2.9k
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1
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2.0k
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Comment: Comment: Dante vs Nebula indexcov
2.7 years ago by German.M.Demidov ★ 2.9k
1
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0
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679
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Answer: Answer: Effect of unequal sample sizes on p-value
2.7 years ago by German.M.Demidov ★ 2.9k
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1
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2.2k
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Comment: Comment: very low coverage when mappin genomic DNA
2.7 years ago by German.M.Demidov ★ 2.9k
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0
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2.2k
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Comment: Comment: very low coverage when mappin genomic DNA
2.7 years ago by German.M.Demidov ★ 2.9k
1
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0
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752
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Comment: Comment: How to merge multiple patient's vcf files (indel and snv) with different IDs?
2.7 years ago by German.M.Demidov ★ 2.9k
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2
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2.2k
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Comment: Comment: very low coverage when mappin genomic DNA
2.7 years ago by German.M.Demidov ★ 2.9k
1
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1
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1.1k
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Comment: Comment: Need suggestions about pathogenicity prediction of gdc level 3 SNV file
2.7 years ago by German.M.Demidov ★ 2.9k
1
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1
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1.1k
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Comment: Comment: Need suggestions about pathogenicity prediction of gdc level 3 SNV file
2.7 years ago by German.M.Demidov ★ 2.9k
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1
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2.5k
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Comment: Comment: gender determination and chrX CN calls
2.7 years ago by German.M.Demidov ★ 2.9k
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1
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2.5k
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Comment: Comment: gender determination and chrX CN calls
2.7 years ago by German.M.Demidov ★ 2.9k
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1
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2.5k
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Comment: Comment: gender determination and chrX CN calls
2.7 years ago by German.M.Demidov ★ 2.9k
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0
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2.4k
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Comment: Comment: Default CNV call thresholds for haplotype chromosome s
2.7 years ago by German.M.Demidov ★ 2.9k
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1
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1.9k
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Answer: Answer: Inferring CNVs from BAM files with SAMTools depth
2.7 years ago by German.M.Demidov ★ 2.9k
1
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0
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1.9k
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Comment: Comment: Inferring CNVs from BAM files with SAMTools depth
2.7 years ago by German.M.Demidov ★ 2.9k
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1
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1.9k
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Comment: Comment: Inferring CNVs from BAM files with SAMTools depth
2.7 years ago by German.M.Demidov ★ 2.9k
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0
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635
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KING struggle: Relatedness
king relatedness
2.7 years ago by German.M.Demidov ★ 2.9k
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1
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2.4k
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Comment: Comment: Default CNV call thresholds for haplotype chromosome s
2.7 years ago by German.M.Demidov ★ 2.9k
0
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1
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2.4k
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Comment: Comment: Default CNV call thresholds for haplotype chromosome s
2.7 years ago by German.M.Demidov ★ 2.9k
0
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1
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2.4k
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Comment: Comment: Default CNV call thresholds for haplotype chromosome s
2.7 years ago by German.M.Demidov ★ 2.9k
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0
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1.3k
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Comment: Comment: Where do I get a WES dataset of size <1GB
2.7 years ago by German.M.Demidov ★ 2.9k
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1
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1.3k
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Comment: Comment: Where do I get a WES dataset of size <1GB
2.7 years ago by German.M.Demidov ★ 2.9k
0
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1
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2.4k
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Comment: Comment: Default CNV call thresholds for haplotype chromosome s
2.7 years ago by German.M.Demidov ★ 2.9k
0
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1
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748
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Comment: Comment: Genotyping variants from BAM (human)
2.7 years ago by German.M.Demidov ★ 2.9k
2
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3
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748
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Genotyping variants from BAM (human)
genotyping
updated 2.7 years ago by 142k • written 2.7 years ago by ★ 2.9k
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2.4k
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Comment: Comment: Default CNV call thresholds for haplotype chromosome s
2.7 years ago by German.M.Demidov ★ 2.9k
0
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1
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2.4k
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Comment: Comment: Default CNV call thresholds for haplotype chromosome s
2.7 years ago by German.M.Demidov ★ 2.9k
3
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0
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763
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Comment: Comment: Is reclustering of a cluster obtained from hierarchical clustering "allowed"?
2.7 years ago by German.M.Demidov ★ 2.9k
1
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0
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2.5k
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Comment: Comment: Why is WGS/WES depth of Y chromosome highly variable?
2.8 years ago by German.M.Demidov ★ 2.9k
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1
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2.5k
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Comment: Comment: Why is WGS/WES depth of Y chromosome highly variable?
2.8 years ago by German.M.Demidov ★ 2.9k
0
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1
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652
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Comment: Comment: Should I run GISTIC2.0 for cases/controls separately?
2.8 years ago by German.M.Demidov ★ 2.9k
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1
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2.5k
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Comment: Comment: Why is WGS/WES depth of Y chromosome highly variable?
2.8 years ago by German.M.Demidov ★ 2.9k
0
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1
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2.5k
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Comment: Comment: Why is WGS/WES depth of Y chromosome highly variable?
2.8 years ago by German.M.Demidov ★ 2.9k
0
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0
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1.2k
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Comment: Comment: Considering the multiple test correction for the analysis of polygenic risk scor
2.8 years ago by German.M.Demidov ★ 2.9k
0
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1
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1.2k
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Comment: Comment: Considering the multiple test correction for the analysis of polygenic risk scor
2.8 years ago by German.M.Demidov ★ 2.9k
0
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1
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1.2k
views
Comment: Comment: Considering the multiple test correction for the analysis of polygenic risk scor
2.8 years ago by German.M.Demidov ★ 2.9k
0
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1
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2.5k
views
Comment: Comment: Why is WGS/WES depth of Y chromosome highly variable?
2.8 years ago by German.M.Demidov ★ 2.9k
1
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1
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1.8k
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Comment: Comment: Collect COV file by BedCoverage
2.8 years ago by German.M.Demidov ★ 2.9k
0
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1
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708
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Comment: Comment: Linear versus affine gap cost
2.8 years ago by German.M.Demidov ★ 2.9k
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