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Comment: Comment: How to interpret arcs in the Sashimi plots (IGV)?
2.3 years ago by German.M.Demidov ★ 2.9k
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1.3k
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Comment: Comment: How to interpret arcs in the Sashimi plots (IGV)?
2.3 years ago by German.M.Demidov ★ 2.9k
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1
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726
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Comment: Comment: RNA-Seq, mutation , copy numnber
2.3 years ago by German.M.Demidov ★ 2.9k
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1
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695
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Comment: Comment: Extract allelic depths in a BAM
2.3 years ago by German.M.Demidov ★ 2.9k
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974
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Comment: Comment: Very high variant similarity between a couple
2.3 years ago by German.M.Demidov ★ 2.9k
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1
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974
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Comment: Comment: Very high variant similarity between a couple
2.3 years ago by German.M.Demidov ★ 2.9k
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1.2k
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Comment: Comment: SNPs significant in all Plink tests
2.3 years ago by German.M.Demidov ★ 2.9k
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1
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1.2k
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Comment: Comment: SNPs significant in all Plink tests
2.3 years ago by German.M.Demidov ★ 2.9k
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1
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1.2k
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Comment: Comment: SNPs significant in all Plink tests
2.3 years ago by German.M.Demidov ★ 2.9k
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1
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1.2k
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Comment: Comment: SNPs significant in all Plink tests
2.3 years ago by German.M.Demidov ★ 2.9k
1
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1
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919
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Comment: Comment: Meaning of allele frequency
2.3 years ago by German.M.Demidov ★ 2.9k
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472
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Comment: Comment: low coverage genome compare to the exome with respect to the level of coverage a
2.3 years ago by German.M.Demidov ★ 2.9k
3
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1
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827
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Comment: Comment: 60X coverage_genomic coverage vary
2.3 years ago by German.M.Demidov ★ 2.9k
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0
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691
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Comment: Comment: How to edit a VCF file in python
2.3 years ago by German.M.Demidov ★ 2.9k
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1
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1.1k
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Comment: Comment: CNV detection for amplicon sequence datas without bed file
2.3 years ago by German.M.Demidov ★ 2.9k
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0
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704
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Comment: Comment: CNV calling, copy number calling, using ONLY Log2R values (with segmentation
2.3 years ago by German.M.Demidov ★ 2.9k
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549
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Comment: Comment: Fisher test in R to compare percentages of three databases
2.4 years ago by German.M.Demidov ★ 2.9k
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0
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510
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Comment: Comment: Reference material for distinguishing focal CNV and chromosome CNV
2.4 years ago by German.M.Demidov ★ 2.9k
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4.7k
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Comment: Comment: Copy Number Variation Tools
2.4 years ago by German.M.Demidov ★ 2.9k
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0
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663
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Comment: Comment: How to get copy number of gene from WGS data?
2.4 years ago by German.M.Demidov ★ 2.9k
1
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1
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895
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Comment: Comment: HPO Terms using OMIM IDs
2.5 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: Isolate a Region in a Vcf File to make a Smaller Vcf File
2.7 years ago by German.M.Demidov ★ 2.9k
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3.4k
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Comment: Comment: Problem with viewing BAM files in IGV
2.7 years ago by German.M.Demidov ★ 2.9k
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1
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3.4k
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Comment: Comment: Problem with viewing BAM files in IGV
2.7 years ago by German.M.Demidov ★ 2.9k
0
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1
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3.4k
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Comment: Comment: Problem with viewing BAM files in IGV
2.7 years ago by German.M.Demidov ★ 2.9k
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0
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1.4k
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Comment: Comment: Why some SNP's are not assigned to any gene?
2.7 years ago by German.M.Demidov ★ 2.9k
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0
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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
2
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1
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1.4k
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Comment: Comment: Why some SNP's are not assigned to any gene?
2.7 years ago by German.M.Demidov ★ 2.9k
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0
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1.2k
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Comment: Comment: Dragen-gatk pipeline information ?
2.7 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: Dragen-gatk pipeline information ?
2.7 years ago by German.M.Demidov ★ 2.9k
1
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1
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731
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Comment: Comment: custom reference panel
2.7 years ago by German.M.Demidov ★ 2.9k
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2.4k
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Comment: Comment: Filtering long indels from VCF
2.7 years ago by German.M.Demidov ★ 2.9k
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1
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1.0k
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Comment: Comment: Allele frequency for genes
2.7 years ago by German.M.Demidov ★ 2.9k
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1
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1.0k
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Comment: Comment: Allele frequency for genes
2.7 years ago by German.M.Demidov ★ 2.9k
1
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0
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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
2.7 years ago by German.M.Demidov ★ 2.9k
0
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0
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828
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Comment: Comment: Variant Allele Frequency
2.7 years ago by German.M.Demidov ★ 2.9k
0
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0
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564
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Comment: Comment: How is better perform the analyze the somatic mutations? (the mutations of my in
2.7 years ago by German.M.Demidov ★ 2.9k
0
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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
0
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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
1
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0
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850
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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
0
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1
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726
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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
0
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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
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
0
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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
0
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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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755
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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
0
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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
565 results • Page 2 of 12
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