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Comment: Comment: Allele count of 2 for homoplasmic MT variants in VCF
6 months ago by Arton ▴ 20
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Comment: Comment: Filtering VCF files based on VAF giving incorrect results
6 months ago by Arton ▴ 20
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Comment: Comment: Using VEP annotation output as the input for a second VEP annotation
6 months ago by Arton ▴ 20
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Comment: Comment: How to calculate coverage of Nanopore long read data?
6 months ago by Arton ▴ 20
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558
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Comment: Comment: I can't add VAF from population for all of my variants from VCF file
8 months ago by Arton ▴ 20
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Comment: Comment: index fasta file for HaplotypeCaller
8 months ago by Arton ▴ 20
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Comment: Comment: How to merge VCF files from multiple samples and remove individual level informa
8 months ago by Arton ▴ 20
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620
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Comment: Comment: How to merge VCF files from multiple samples and remove individual level informa
9 months ago by Arton ▴ 20
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2.3k
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Comment: Comment: How to calculate coverage of Nanopore long read data?
10 months ago by Arton ▴ 20
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974
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Comment: Comment: Using VEP annotation output as the input for a second VEP annotation
10 months ago by Arton ▴ 20
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974
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Comment: Comment: Using VEP annotation output as the input for a second VEP annotation
10 months ago by Arton ▴ 20
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974
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Comment: Comment: Using VEP annotation output as the input for a second VEP annotation
updated 10 months ago by 44k • written 10 months ago by ▴ 20
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Comment: Comment: How to calculate coverage of Nanopore long read data?
23 months ago by Arton ▴ 20
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1.1k
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Comment: Comment: NCBI reported coverage from long and short reads
23 months ago by Arton ▴ 20
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4.4k
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Comment: Comment: Where To Get The Genetic Map For The Haplotype Reference Consortium to phase the
3.0 years ago by Arton ▴ 20
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