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Comment: Comment: Filtering long indels from VCF
4.1 years ago by German.M.Demidov ★ 3.0k
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1
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1.6k
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Comment: Comment: Allele frequency for genes
4.1 years ago by German.M.Demidov ★ 3.0k
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1
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1.6k
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Comment: Comment: Allele frequency for genes
4.1 years ago by German.M.Demidov ★ 3.0k
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6.8k
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Comment: Comment: How to estimate polygenic risk score (PRSs) using the scoring files from PGSCata
4.1 years ago by German.M.Demidov ★ 3.0k
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1.3k
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Comment: Comment: Variant Allele Frequency
4.1 years ago by German.M.Demidov ★ 3.0k
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904
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Comment: Comment: How is better perform the analyze the somatic mutations? (the mutations of my in
4.1 years ago by German.M.Demidov ★ 3.0k
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1
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2.1k
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Comment: Comment: Rare variant association analysis (SKAT-O) - Power calculation
4.1 years ago by German.M.Demidov ★ 3.0k
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1
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2.1k
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Comment: Comment: Rare variant association analysis (SKAT-O) - Power calculation
4.1 years ago by German.M.Demidov ★ 3.0k
1
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0
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1.4k
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Comment: Comment: Germline Cancer Mutations
4.1 years ago by German.M.Demidov ★ 3.0k
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1
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4.6k
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Comment: Comment: Dealing with P value inflation of SNPs identified by qqplot
4.1 years ago by German.M.Demidov ★ 3.0k
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1
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1.1k
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Comment: Comment: Regarding p53 (tumour suppressor gene) mutation and overexpression relation with
4.2 years ago by German.M.Demidov ★ 3.0k
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1
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4.6k
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Comment: Comment: Dealing with P value inflation of SNPs identified by qqplot
4.2 years ago by German.M.Demidov ★ 3.0k
0
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1
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2.9k
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Comment: Comment: Dante vs Nebula indexcov
4.2 years ago by German.M.Demidov ★ 3.0k
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1
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2.9k
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Comment: Comment: Dante vs Nebula indexcov
4.2 years ago by German.M.Demidov ★ 3.0k
1
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1.1k
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Answer: Answer: Effect of unequal sample sizes on p-value
4.2 years ago by German.M.Demidov ★ 3.0k
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1
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3.6k
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Comment: Comment: very low coverage when mappin genomic DNA
4.2 years ago by German.M.Demidov ★ 3.0k
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0
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3.6k
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Comment: Comment: very low coverage when mappin genomic DNA
4.2 years ago by German.M.Demidov ★ 3.0k
1
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0
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1.1k
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Comment: Comment: How to merge multiple patient's vcf files (indel and snv) with different IDs?
4.2 years ago by German.M.Demidov ★ 3.0k
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2
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3.6k
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Comment: Comment: very low coverage when mappin genomic DNA
4.2 years ago by German.M.Demidov ★ 3.0k
1
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1
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1.6k
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Comment: Comment: Need suggestions about pathogenicity prediction of gdc level 3 SNV file
4.2 years ago by German.M.Demidov ★ 3.0k
1
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1
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1.6k
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Comment: Comment: Need suggestions about pathogenicity prediction of gdc level 3 SNV file
4.2 years ago by German.M.Demidov ★ 3.0k
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1
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4.0k
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Comment: Comment: gender determination and chrX CN calls
4.2 years ago by German.M.Demidov ★ 3.0k
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1
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4.0k
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Comment: Comment: gender determination and chrX CN calls
4.2 years ago by German.M.Demidov ★ 3.0k
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1
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4.0k
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Comment: Comment: gender determination and chrX CN calls
4.2 years ago by German.M.Demidov ★ 3.0k
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0
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3.6k
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Comment: Comment: Default CNV call thresholds for haplotype chromosome s
4.2 years ago by German.M.Demidov ★ 3.0k
2
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1
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3.0k
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Answer: Answer: Inferring CNVs from BAM files with SAMTools depth
4.2 years ago by German.M.Demidov ★ 3.0k
1
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0
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3.0k
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Comment: Comment: Inferring CNVs from BAM files with SAMTools depth
4.2 years ago by German.M.Demidov ★ 3.0k
0
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1
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3.0k
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Comment: Comment: Inferring CNVs from BAM files with SAMTools depth
4.2 years ago by German.M.Demidov ★ 3.0k
0
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0
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916
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KING struggle: Relatedness
king relatedness
4.2 years ago by German.M.Demidov ★ 3.0k
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1
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3.6k
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Comment: Comment: Default CNV call thresholds for haplotype chromosome s
4.2 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: Default CNV call thresholds for haplotype chromosome s
4.2 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: Default CNV call thresholds for haplotype chromosome s
4.2 years ago by German.M.Demidov ★ 3.0k
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0
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2.1k
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Comment: Comment: Where do I get a WES dataset of size <1GB
4.2 years ago by German.M.Demidov ★ 3.0k
0
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1
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2.1k
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Comment: Comment: Where do I get a WES dataset of size <1GB
4.2 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: Default CNV call thresholds for haplotype chromosome s
4.2 years ago by German.M.Demidov ★ 3.0k
0
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1
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1.2k
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Comment: Comment: Genotyping variants from BAM (human)
4.2 years ago by German.M.Demidov ★ 3.0k
2
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3
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1.2k
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Genotyping variants from BAM (human)
genotyping
updated 4.2 years ago by 154k • written 4.2 years ago by ★ 3.0k
0
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1
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3.6k
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Comment: Comment: Default CNV call thresholds for haplotype chromosome s
4.2 years ago by German.M.Demidov ★ 3.0k
0
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1
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3.6k
views
Comment: Comment: Default CNV call thresholds for haplotype chromosome s
4.2 years ago by German.M.Demidov ★ 3.0k
3
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0
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1.1k
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Comment: Comment: Is reclustering of a cluster obtained from hierarchical clustering "allowed"?
4.2 years ago by German.M.Demidov ★ 3.0k
1
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0
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4.1k
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Comment: Comment: Why is WGS/WES depth of Y chromosome highly variable?
4.2 years ago by German.M.Demidov ★ 3.0k
0
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1
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4.1k
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Comment: Comment: Why is WGS/WES depth of Y chromosome highly variable?
4.2 years ago by German.M.Demidov ★ 3.0k
0
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1
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1.1k
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Comment: Comment: Should I run GISTIC2.0 for cases/controls separately?
4.2 years ago by German.M.Demidov ★ 3.0k
0
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1
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4.1k
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Comment: Comment: Why is WGS/WES depth of Y chromosome highly variable?
4.2 years ago by German.M.Demidov ★ 3.0k
0
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1
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4.1k
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Comment: Comment: Why is WGS/WES depth of Y chromosome highly variable?
4.2 years ago by German.M.Demidov ★ 3.0k
0
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0
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1.9k
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Comment: Comment: Considering the multiple test correction for the analysis of polygenic risk scor
4.2 years ago by German.M.Demidov ★ 3.0k
0
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1
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1.9k
views
Comment: Comment: Considering the multiple test correction for the analysis of polygenic risk scor
4.3 years ago by German.M.Demidov ★ 3.0k
0
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1
reply
1.9k
views
Comment: Comment: Considering the multiple test correction for the analysis of polygenic risk scor
4.3 years ago by German.M.Demidov ★ 3.0k
0
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1
reply
4.1k
views
Comment: Comment: Why is WGS/WES depth of Y chromosome highly variable?
4.3 years ago by German.M.Demidov ★ 3.0k
1
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2
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3.1k
views
Answer: Answer: Collect COV file by BedCoverage
4.3 years ago by German.M.Demidov ★ 3.0k
657 results • Page 3 of 14
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