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Array variant to reference-standard way
genotyping
9 days ago by German.M.Demidov ★ 2.5k
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244
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Comment: Comment: Isolate a Region in a Vcf File to make a Smaller Vcf File
28 days ago by German.M.Demidov ★ 2.5k
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316
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Comment: Comment: Problem with viewing BAM files in IGV
28 days ago by German.M.Demidov ★ 2.5k
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316
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Comment: Comment: Problem with viewing BAM files in IGV
28 days ago by German.M.Demidov ★ 2.5k
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1
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316
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Comment: Comment: Problem with viewing BAM files in IGV
28 days ago by German.M.Demidov ★ 2.5k
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520
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Comment: Comment: Why some SNP's are not assigned to any gene?
4 weeks ago by German.M.Demidov ★ 2.5k
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355
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Comment: Comment: Dealing with P value inflation of SNPs identified by qqplot
4 weeks ago by German.M.Demidov ★ 2.5k
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1
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520
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Comment: Comment: Why some SNP's are not assigned to any gene?
4 weeks ago by German.M.Demidov ★ 2.5k
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248
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Comment: Comment: Dragen-gatk pipeline information ?
5 weeks ago by German.M.Demidov ★ 2.5k
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1
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248
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Comment: Comment: Dragen-gatk pipeline information ?
5 weeks ago by German.M.Demidov ★ 2.5k
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1
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196
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Comment: Comment: custom reference panel
5 weeks ago by German.M.Demidov ★ 2.5k
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192
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Comment: Comment: Filtering long indels from VCF
5 weeks ago by German.M.Demidov ★ 2.5k
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3
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192
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Filtering long indels from VCF
VCF
5 weeks ago by German.M.Demidov ★ 2.5k
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1
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281
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Comment: Comment: Allele frequency for genes
5 weeks ago by German.M.Demidov ★ 2.5k
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1
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281
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Comment: Comment: Allele frequency for genes
5 weeks ago by German.M.Demidov ★ 2.5k
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112
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Comment: Comment: What are the classifications of Molecular Pathology Services?
5 weeks ago by German.M.Demidov ★ 2.5k
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847
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Comment: Comment: How to estimate polygenic risk score (PRSs) using the scoring files from PGSCata
5 weeks ago by German.M.Demidov ★ 2.5k
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223
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Comment: Comment: Variant Allele Frequency
5 weeks ago by German.M.Demidov ★ 2.5k
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124
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Comment: Comment: How is better perform the analyze the somatic mutations? (the mutations of my in
5 weeks ago by German.M.Demidov ★ 2.5k
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1
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240
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Comment: Comment: Rare variant association analysis (SKAT-O) - Power calculation
6 weeks ago by German.M.Demidov ★ 2.5k
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1
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240
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Comment: Comment: Rare variant association analysis (SKAT-O) - Power calculation
6 weeks ago by German.M.Demidov ★ 2.5k
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0
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215
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Comment: Comment: Germline Cancer Mutations
6 weeks ago by German.M.Demidov ★ 2.5k
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1
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355
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Comment: Comment: Dealing with P value inflation of SNPs identified by qqplot
6 weeks ago by German.M.Demidov ★ 2.5k
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1
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314
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Comment: Comment: Regarding p53 (tumour suppressor gene) mutation and overexpression relation with
6 weeks ago by German.M.Demidov ★ 2.5k
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1
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355
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Comment: Comment: Dealing with P value inflation of SNPs identified by qqplot
6 weeks ago by German.M.Demidov ★ 2.5k
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1
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558
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Comment: Comment: Dante vs Nebula indexcov
7 weeks ago by German.M.Demidov ★ 2.5k
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1
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558
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Comment: Comment: Dante vs Nebula indexcov
8 weeks ago by German.M.Demidov ★ 2.5k
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0
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129
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Answer: Answer: Effect of unequal sample sizes on p-value
8 weeks ago by German.M.Demidov ★ 2.5k
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1
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692
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Comment: Comment: very low coverage when mappin genomic DNA
8 weeks ago by German.M.Demidov ★ 2.5k
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0
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692
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Comment: Comment: very low coverage when mappin genomic DNA
8 weeks ago by German.M.Demidov ★ 2.5k
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0
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143
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Comment: Comment: How to merge multiple patient's vcf files (indel and snv) with different IDs?
8 weeks ago by German.M.Demidov ★ 2.5k
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2
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692
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Comment: Comment: very low coverage when mappin genomic DNA
8 weeks ago by German.M.Demidov ★ 2.5k
1
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1
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350
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Comment: Comment: Need suggestions about pathogenicity prediction of gdc level 3 SNV file
8 weeks ago by German.M.Demidov ★ 2.5k
1
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1
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350
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Comment: Comment: Need suggestions about pathogenicity prediction of gdc level 3 SNV file
8 weeks ago by German.M.Demidov ★ 2.5k
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1
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730
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Comment: Comment: gender determination and chrX CN calls
8 weeks ago by German.M.Demidov ★ 2.5k
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1
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730
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Comment: Comment: gender determination and chrX CN calls
8 weeks ago by German.M.Demidov ★ 2.5k
0
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1
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730
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Comment: Comment: gender determination and chrX CN calls
9 weeks ago by German.M.Demidov ★ 2.5k
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0
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716
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Comment: Comment: Default CNV call thresholds for haplotype chromosome s
9 weeks ago by German.M.Demidov ★ 2.5k
1
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1
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424
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Answer: Answer: Inferring CNVs from BAM files with SAMTools depth
9 weeks ago by German.M.Demidov ★ 2.5k
1
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0
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424
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Comment: Comment: Inferring CNVs from BAM files with SAMTools depth
9 weeks ago by German.M.Demidov ★ 2.5k
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1
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424
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Comment: Comment: Inferring CNVs from BAM files with SAMTools depth
9 weeks ago by German.M.Demidov ★ 2.5k
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0
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119
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KING struggle: Relatedness
king relatedness
9 weeks ago by German.M.Demidov ★ 2.5k
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1
reply
716
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Comment: Comment: Default CNV call thresholds for haplotype chromosome s
9 weeks ago by German.M.Demidov ★ 2.5k
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1
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716
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Comment: Comment: Default CNV call thresholds for haplotype chromosome s
10 weeks ago by German.M.Demidov ★ 2.5k
0
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1
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716
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Comment: Comment: Default CNV call thresholds for haplotype chromosome s
10 weeks ago by German.M.Demidov ★ 2.5k
0
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0
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381
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Comment: Comment: Where do I get a WES dataset of size <1GB
10 weeks ago by German.M.Demidov ★ 2.5k
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1
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381
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Comment: Comment: Where do I get a WES dataset of size <1GB
10 weeks ago by German.M.Demidov ★ 2.5k
0
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1
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716
views
Comment: Comment: Default CNV call thresholds for haplotype chromosome s
10 weeks ago by German.M.Demidov ★ 2.5k
0
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1
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228
views
Comment: Comment: Genotyping variants from BAM (human)
10 weeks ago by German.M.Demidov ★ 2.5k
2
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3
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228
views
Genotyping variants from BAM (human)
genotyping
updated 10 weeks ago by 107k • written 10 weeks ago by ★ 2.5k
577 results • Page 1 of 12
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