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Comment: Comment: Allele frequency for genes
3.8 years ago by German.M.Demidov ★ 3.0k
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1.4k
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Comment: Comment: Allele frequency for genes
3.8 years ago by German.M.Demidov ★ 3.0k
1
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0
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5.5k
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Comment: Comment: How to estimate polygenic risk score (PRSs) using the scoring files from PGSCata
3.8 years ago by German.M.Demidov ★ 3.0k
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1.2k
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Comment: Comment: Variant Allele Frequency
3.8 years ago by German.M.Demidov ★ 3.0k
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0
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772
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Comment: Comment: How is better perform the analyze the somatic mutations? (the mutations of my in
3.8 years ago by German.M.Demidov ★ 3.0k
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1
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1.9k
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Comment: Comment: Rare variant association analysis (SKAT-O) - Power calculation
3.8 years ago by German.M.Demidov ★ 3.0k
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1
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1.9k
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Comment: Comment: Rare variant association analysis (SKAT-O) - Power calculation
3.8 years ago by German.M.Demidov ★ 3.0k
1
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0
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1.2k
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Comment: Comment: Germline Cancer Mutations
3.8 years ago by German.M.Demidov ★ 3.0k
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1
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4.3k
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Comment: Comment: Dealing with P value inflation of SNPs identified by qqplot
3.8 years ago by German.M.Demidov ★ 3.0k
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1
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957
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Comment: Comment: Regarding p53 (tumour suppressor gene) mutation and overexpression relation with
3.8 years ago by German.M.Demidov ★ 3.0k
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1
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4.3k
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Comment: Comment: Dealing with P value inflation of SNPs identified by qqplot
3.8 years ago by German.M.Demidov ★ 3.0k
0
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1
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2.6k
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Comment: Comment: Dante vs Nebula indexcov
3.8 years ago by German.M.Demidov ★ 3.0k
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1
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2.6k
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Comment: Comment: Dante vs Nebula indexcov
3.8 years ago by German.M.Demidov ★ 3.0k
1
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0
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998
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Answer: Answer: Effect of unequal sample sizes on p-value
3.8 years ago by German.M.Demidov ★ 3.0k
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1
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3.2k
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Comment: Comment: very low coverage when mappin genomic DNA
3.8 years ago by German.M.Demidov ★ 3.0k
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0
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3.2k
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Comment: Comment: very low coverage when mappin genomic DNA
3.8 years ago by German.M.Demidov ★ 3.0k
1
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0
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1.0k
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Comment: Comment: How to merge multiple patient's vcf files (indel and snv) with different IDs?
3.8 years ago by German.M.Demidov ★ 3.0k
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2
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3.2k
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Comment: Comment: very low coverage when mappin genomic DNA
3.8 years ago by German.M.Demidov ★ 3.0k
1
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1
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1.5k
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Comment: Comment: Need suggestions about pathogenicity prediction of gdc level 3 SNV file
3.8 years ago by German.M.Demidov ★ 3.0k
1
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1
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1.5k
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Comment: Comment: Need suggestions about pathogenicity prediction of gdc level 3 SNV file
3.8 years ago by German.M.Demidov ★ 3.0k
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1
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3.4k
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Comment: Comment: gender determination and chrX CN calls
3.8 years ago by German.M.Demidov ★ 3.0k
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1
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3.4k
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Comment: Comment: gender determination and chrX CN calls
3.8 years ago by German.M.Demidov ★ 3.0k
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1
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3.4k
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Comment: Comment: gender determination and chrX CN calls
3.8 years ago by German.M.Demidov ★ 3.0k
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0
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3.2k
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Comment: Comment: Default CNV call thresholds for haplotype chromosome s
3.8 years ago by German.M.Demidov ★ 3.0k
2
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1
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2.6k
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Answer: Answer: Inferring CNVs from BAM files with SAMTools depth
3.8 years ago by German.M.Demidov ★ 3.0k
1
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0
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2.6k
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Comment: Comment: Inferring CNVs from BAM files with SAMTools depth
3.8 years ago by German.M.Demidov ★ 3.0k
0
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1
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2.6k
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Comment: Comment: Inferring CNVs from BAM files with SAMTools depth
3.8 years ago by German.M.Demidov ★ 3.0k
0
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0
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837
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KING struggle: Relatedness
king relatedness
3.8 years ago by German.M.Demidov ★ 3.0k
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1
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3.2k
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Comment: Comment: Default CNV call thresholds for haplotype chromosome s
3.8 years ago by German.M.Demidov ★ 3.0k
0
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1
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3.2k
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Comment: Comment: Default CNV call thresholds for haplotype chromosome s
3.8 years ago by German.M.Demidov ★ 3.0k
0
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1
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3.2k
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Comment: Comment: Default CNV call thresholds for haplotype chromosome s
3.8 years ago by German.M.Demidov ★ 3.0k
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0
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1.8k
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Comment: Comment: Where do I get a WES dataset of size <1GB
3.8 years ago by German.M.Demidov ★ 3.0k
0
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1
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1.8k
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Comment: Comment: Where do I get a WES dataset of size <1GB
3.8 years ago by German.M.Demidov ★ 3.0k
0
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1
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3.2k
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Comment: Comment: Default CNV call thresholds for haplotype chromosome s
3.9 years ago by German.M.Demidov ★ 3.0k
0
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1
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1.0k
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Comment: Comment: Genotyping variants from BAM (human)
3.9 years ago by German.M.Demidov ★ 3.0k
2
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3
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1.0k
views
Genotyping variants from BAM (human)
genotyping
updated 3.9 years ago by 151k • written 3.9 years ago by ★ 3.0k
0
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1
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3.2k
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Comment: Comment: Default CNV call thresholds for haplotype chromosome s
3.9 years ago by German.M.Demidov ★ 3.0k
0
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1
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3.2k
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Comment: Comment: Default CNV call thresholds for haplotype chromosome s
3.9 years ago by German.M.Demidov ★ 3.0k
3
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0
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981
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Comment: Comment: Is reclustering of a cluster obtained from hierarchical clustering "allowed"?
3.9 years ago by German.M.Demidov ★ 3.0k
1
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0
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3.6k
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Comment: Comment: Why is WGS/WES depth of Y chromosome highly variable?
3.9 years ago by German.M.Demidov ★ 3.0k
0
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1
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3.6k
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Comment: Comment: Why is WGS/WES depth of Y chromosome highly variable?
3.9 years ago by German.M.Demidov ★ 3.0k
0
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1
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912
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Comment: Comment: Should I run GISTIC2.0 for cases/controls separately?
3.9 years ago by German.M.Demidov ★ 3.0k
0
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1
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3.6k
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Comment: Comment: Why is WGS/WES depth of Y chromosome highly variable?
3.9 years ago by German.M.Demidov ★ 3.0k
0
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1
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3.6k
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Comment: Comment: Why is WGS/WES depth of Y chromosome highly variable?
3.9 years ago by German.M.Demidov ★ 3.0k
0
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0
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1.7k
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Comment: Comment: Considering the multiple test correction for the analysis of polygenic risk scor
3.9 years ago by German.M.Demidov ★ 3.0k
0
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1
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1.7k
views
Comment: Comment: Considering the multiple test correction for the analysis of polygenic risk scor
3.9 years ago by German.M.Demidov ★ 3.0k
0
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1
reply
1.7k
views
Comment: Comment: Considering the multiple test correction for the analysis of polygenic risk scor
3.9 years ago by German.M.Demidov ★ 3.0k
0
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1
reply
3.6k
views
Comment: Comment: Why is WGS/WES depth of Y chromosome highly variable?
3.9 years ago by German.M.Demidov ★ 3.0k
1
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1
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2.6k
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Comment: Comment: Collect COV file by BedCoverage
3.9 years ago by German.M.Demidov ★ 3.0k
0
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1
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999
views
Comment: Comment: Linear versus affine gap cost
3.9 years ago by German.M.Demidov ★ 3.0k
656 results • Page 3 of 14
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