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Comment: Comment: How to interpret arcs in the Sashimi plots (IGV)?
2.7 years ago by German.M.Demidov ★ 2.9k
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1.5k
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Comment: Comment: How to interpret arcs in the Sashimi plots (IGV)?
2.7 years ago by German.M.Demidov ★ 2.9k
1
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1
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805
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Comment: Comment: RNA-Seq, mutation , copy numnber
2.7 years ago by German.M.Demidov ★ 2.9k
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1
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770
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Comment: Comment: Extract allelic depths in a BAM
2.7 years ago by German.M.Demidov ★ 2.9k
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1.1k
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Comment: Comment: Very high variant similarity between a couple
2.7 years ago by German.M.Demidov ★ 2.9k
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1.1k
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Comment: Comment: Very high variant similarity between a couple
2.7 years ago by German.M.Demidov ★ 2.9k
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1.4k
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Comment: Comment: SNPs significant in all Plink tests
2.7 years ago by German.M.Demidov ★ 2.9k
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1
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1.4k
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Comment: Comment: SNPs significant in all Plink tests
2.7 years ago by German.M.Demidov ★ 2.9k
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1.4k
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Comment: Comment: SNPs significant in all Plink tests
2.7 years ago by German.M.Demidov ★ 2.9k
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1
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1.4k
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Comment: Comment: SNPs significant in all Plink tests
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: Meaning of allele frequency
2.7 years ago by German.M.Demidov ★ 2.9k
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533
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Comment: Comment: low coverage genome compare to the exome with respect to the level of coverage a
2.7 years ago by German.M.Demidov ★ 2.9k
3
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1
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928
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Comment: Comment: 60X coverage_genomic coverage vary
2.7 years ago by German.M.Demidov ★ 2.9k
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0
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773
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Comment: Comment: How to edit a VCF file in python
2.7 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: CNV detection for amplicon sequence datas without bed file
2.7 years ago by German.M.Demidov ★ 2.9k
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834
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Comment: Comment: CNV calling, copy number calling, using ONLY Log2R values (with segmentation
2.7 years ago by German.M.Demidov ★ 2.9k
1
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623
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Comment: Comment: Fisher test in R to compare percentages of three databases
2.8 years ago by German.M.Demidov ★ 2.9k
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0
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581
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Comment: Comment: Reference material for distinguishing focal CNV and chromosome CNV
2.8 years ago by German.M.Demidov ★ 2.9k
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5.0k
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Comment: Comment: Copy Number Variation Tools
2.8 years ago by German.M.Demidov ★ 2.9k
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0
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730
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Comment: Comment: How to get copy number of gene from WGS data?
2.8 years ago by German.M.Demidov ★ 2.9k
1
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1
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988
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Comment: Comment: HPO Terms using OMIM IDs
2.9 years ago by German.M.Demidov ★ 2.9k
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1
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1.5k
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Comment: Comment: Isolate a Region in a Vcf File to make a Smaller Vcf File
3.1 years ago by German.M.Demidov ★ 2.9k
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0
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4.3k
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Comment: Comment: Problem with viewing BAM files in IGV
3.1 years ago by German.M.Demidov ★ 2.9k
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1
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4.3k
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Comment: Comment: Problem with viewing BAM files in IGV
3.1 years ago by German.M.Demidov ★ 2.9k
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1
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4.3k
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Comment: Comment: Problem with viewing BAM files in IGV
3.1 years ago by German.M.Demidov ★ 2.9k
1
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0
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1.6k
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Comment: Comment: Why some SNP's are not assigned to any gene?
3.1 years ago by German.M.Demidov ★ 2.9k
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0
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3.4k
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Comment: Comment: Dealing with P value inflation of SNPs identified by qqplot
3.1 years ago by German.M.Demidov ★ 2.9k
2
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1
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1.6k
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Comment: Comment: Why some SNP's are not assigned to any gene?
3.1 years ago by German.M.Demidov ★ 2.9k
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0
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1.3k
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Comment: Comment: Dragen-gatk pipeline information ?
3.1 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: Dragen-gatk pipeline information ?
3.1 years ago by German.M.Demidov ★ 2.9k
1
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1
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817
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Comment: Comment: custom reference panel
3.1 years ago by German.M.Demidov ★ 2.9k
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0
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3.0k
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Comment: Comment: Filtering long indels from VCF
3.1 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: Allele frequency for genes
3.1 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: Allele frequency for genes
3.1 years ago by German.M.Demidov ★ 2.9k
1
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0
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4.5k
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Comment: Comment: How to estimate polygenic risk score (PRSs) using the scoring files from PGSCata
3.1 years ago by German.M.Demidov ★ 2.9k
0
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0
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915
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Comment: Comment: Variant Allele Frequency
3.1 years ago by German.M.Demidov ★ 2.9k
0
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0
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626
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Comment: Comment: How is better perform the analyze the somatic mutations? (the mutations of my in
3.1 years ago by German.M.Demidov ★ 2.9k
0
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1
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1.5k
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Comment: Comment: Rare variant association analysis (SKAT-O) - Power calculation
3.1 years ago by German.M.Demidov ★ 2.9k
0
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1
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1.5k
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Comment: Comment: Rare variant association analysis (SKAT-O) - Power calculation
3.1 years ago by German.M.Demidov ★ 2.9k
1
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0
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958
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Comment: Comment: Germline Cancer Mutations
3.1 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: Dealing with P value inflation of SNPs identified by qqplot
3.1 years ago by German.M.Demidov ★ 2.9k
0
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1
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806
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Comment: Comment: Regarding p53 (tumour suppressor gene) mutation and overexpression relation with
3.1 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: Dealing with P value inflation of SNPs identified by qqplot
3.1 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: Dante vs Nebula indexcov
3.1 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: Dante vs Nebula indexcov
3.1 years ago by German.M.Demidov ★ 2.9k
0
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1
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2.5k
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Comment: Comment: very low coverage when mappin genomic DNA
3.1 years ago by German.M.Demidov ★ 2.9k
0
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0
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2.5k
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Comment: Comment: very low coverage when mappin genomic DNA
3.1 years ago by German.M.Demidov ★ 2.9k
1
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0
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844
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Comment: Comment: How to merge multiple patient's vcf files (indel and snv) with different IDs?
3.1 years ago by German.M.Demidov ★ 2.9k
0
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2
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2.5k
views
Comment: Comment: very low coverage when mappin genomic DNA
3.1 years ago by German.M.Demidov ★ 2.9k
1
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1
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1.2k
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Comment: Comment: Need suggestions about pathogenicity prediction of gdc level 3 SNV file
3.1 years ago by German.M.Demidov ★ 2.9k
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