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Comment: Comment: Very high variant similarity between a couple
10 months ago by German.M.Demidov ★ 2.8k
0
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0
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732
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Comment: Comment: SNPs significant in all Plink tests
10 months ago by German.M.Demidov ★ 2.8k
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1
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732
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Comment: Comment: SNPs significant in all Plink tests
10 months ago by German.M.Demidov ★ 2.8k
1
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1
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732
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Comment: Comment: SNPs significant in all Plink tests
10 months ago by German.M.Demidov ★ 2.8k
0
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1
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732
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Comment: Comment: SNPs significant in all Plink tests
10 months ago by German.M.Demidov ★ 2.8k
1
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1
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534
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Comment: Comment: Meaning of allele frequency
10 months ago by German.M.Demidov ★ 2.8k
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0
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264
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Comment: Comment: low coverage genome compare to the exome with respect to the level of coverage a
10 months ago by German.M.Demidov ★ 2.8k
3
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1
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468
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Comment: Comment: 60X coverage_genomic coverage vary
10 months ago by German.M.Demidov ★ 2.8k
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0
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400
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Comment: Comment: How to edit a VCF file in python
10 months ago by German.M.Demidov ★ 2.8k
1
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1
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608
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Comment: Comment: CNV detection for amplicon sequence datas without bed file
10 months ago by German.M.Demidov ★ 2.8k
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0
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362
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Comment: Comment: CNV calling, copy number calling, using ONLY Log2R values (with segmentation
10 months ago by German.M.Demidov ★ 2.8k
1
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0
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310
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Comment: Comment: Fisher test in R to compare percentages of three databases
10 months ago by German.M.Demidov ★ 2.8k
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0
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262
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Comment: Comment: Reference material for distinguishing focal CNV and chromosome CNV
11 months ago by German.M.Demidov ★ 2.8k
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0
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3.9k
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Comment: Comment: Copy Number Variation Tools
11 months ago by German.M.Demidov ★ 2.8k
1
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0
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415
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Comment: Comment: How to get copy number of gene from WGS data?
11 months ago by German.M.Demidov ★ 2.8k
1
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1
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536
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Comment: Comment: HPO Terms using OMIM IDs
12 months ago by German.M.Demidov ★ 2.8k
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0
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256
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Array variant to reference-standard way
genotyping
13 months ago by German.M.Demidov ★ 2.8k
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1
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652
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Comment: Comment: Isolate a Region in a Vcf File to make a Smaller Vcf File
14 months ago by German.M.Demidov ★ 2.8k
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0
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1.2k
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Comment: Comment: Problem with viewing BAM files in IGV
14 months ago by German.M.Demidov ★ 2.8k
1
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1
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1.2k
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Comment: Comment: Problem with viewing BAM files in IGV
14 months ago by German.M.Demidov ★ 2.8k
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1
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1.2k
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Comment: Comment: Problem with viewing BAM files in IGV
14 months ago by German.M.Demidov ★ 2.8k
1
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0
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963
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Comment: Comment: Why some SNP's are not assigned to any gene?
14 months ago by German.M.Demidov ★ 2.8k
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0
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1.6k
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Comment: Comment: Dealing with P value inflation of SNPs identified by qqplot
14 months ago by German.M.Demidov ★ 2.8k
2
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1
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963
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Comment: Comment: Why some SNP's are not assigned to any gene?
14 months ago by German.M.Demidov ★ 2.8k
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0
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717
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Comment: Comment: Dragen-gatk pipeline information ?
14 months ago by German.M.Demidov ★ 2.8k
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1
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717
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Comment: Comment: Dragen-gatk pipeline information ?
14 months ago by German.M.Demidov ★ 2.8k
1
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1
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468
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Comment: Comment: custom reference panel
14 months ago by German.M.Demidov ★ 2.8k
0
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0
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702
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Comment: Comment: Filtering long indels from VCF
14 months ago by German.M.Demidov ★ 2.8k
2
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3
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702
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Filtering long indels from VCF
VCF
14 months ago by German.M.Demidov ★ 2.8k
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1
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671
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Comment: Comment: Allele frequency for genes
14 months ago by German.M.Demidov ★ 2.8k
0
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1
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671
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Comment: Comment: Allele frequency for genes
14 months ago by German.M.Demidov ★ 2.8k
1
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0
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2.3k
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Comment: Comment: How to estimate polygenic risk score (PRSs) using the scoring files from PGSCata
14 months ago by German.M.Demidov ★ 2.8k
0
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0
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530
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Comment: Comment: Variant Allele Frequency
14 months ago by German.M.Demidov ★ 2.8k
0
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0
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354
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Comment: Comment: How is better perform the analyze the somatic mutations? (the mutations of my in
14 months ago by German.M.Demidov ★ 2.8k
0
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1
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730
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Comment: Comment: Rare variant association analysis (SKAT-O) - Power calculation
15 months ago by German.M.Demidov ★ 2.8k
0
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1
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730
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Comment: Comment: Rare variant association analysis (SKAT-O) - Power calculation
15 months ago by German.M.Demidov ★ 2.8k
1
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0
replies
535
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Comment: Comment: Germline Cancer Mutations
15 months ago by German.M.Demidov ★ 2.8k
0
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1
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1.6k
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Comment: Comment: Dealing with P value inflation of SNPs identified by qqplot
15 months ago by German.M.Demidov ★ 2.8k
0
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1
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503
views
Comment: Comment: Regarding p53 (tumour suppressor gene) mutation and overexpression relation with
15 months ago by German.M.Demidov ★ 2.8k
0
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1
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1.6k
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Comment: Comment: Dealing with P value inflation of SNPs identified by qqplot
15 months ago by German.M.Demidov ★ 2.8k
0
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1
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1.4k
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Comment: Comment: Dante vs Nebula indexcov
15 months ago by German.M.Demidov ★ 2.8k
0
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1
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1.4k
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Comment: Comment: Dante vs Nebula indexcov
15 months ago by German.M.Demidov ★ 2.8k
1
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0
replies
403
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Answer: Answer: Effect of unequal sample sizes on p-value
15 months ago by German.M.Demidov ★ 2.8k
0
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1
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1.4k
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Comment: Comment: very low coverage when mappin genomic DNA
15 months ago by German.M.Demidov ★ 2.8k
0
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0
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1.4k
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Comment: Comment: very low coverage when mappin genomic DNA
15 months ago by German.M.Demidov ★ 2.8k
1
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0
replies
400
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Comment: Comment: How to merge multiple patient's vcf files (indel and snv) with different IDs?
15 months ago by German.M.Demidov ★ 2.8k
0
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2
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1.4k
views
Comment: Comment: very low coverage when mappin genomic DNA
15 months ago by German.M.Demidov ★ 2.8k
1
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1
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757
views
Comment: Comment: Need suggestions about pathogenicity prediction of gdc level 3 SNV file
15 months ago by German.M.Demidov ★ 2.8k
1
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1
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757
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Comment: Comment: Need suggestions about pathogenicity prediction of gdc level 3 SNV file
15 months ago by German.M.Demidov ★ 2.8k
0
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1
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1.5k
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Comment: Comment: gender determination and chrX CN calls
15 months ago by German.M.Demidov ★ 2.8k
640 results • Page 2 of 13
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