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Answer: Answer: ANNOVAR doesn't recognize multiple variants at single locus
3.1 years ago by desouzareis.r ▴ 280
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Answer: Answer: Is Human_G1K_V37.Fasta Hg19?
3.1 years ago by desouzareis.r ▴ 280
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Answer: Comment: genotype matrix
3.1 years ago by desouzareis.r ▴ 280
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Answer: Comment: What is the difference between breakends and breakpoints?
3.1 years ago by desouzareis.r ▴ 280
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Answer: Comment: Selecting genotypes for a specific chromosome belonging to a specific patient fr
3.1 years ago by desouzareis.r ▴ 280
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Answer: C: Effect of removing secondary/supplementary alignments from BAM file?
3.1 years ago by desouzareis.r ▴ 280
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Answer: A: Can't create tabix index of the bed file
3.1 years ago by desouzareis.r ▴ 280
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Answer: A: Annotation of pLI scores by using ANNOVAR
3.2 years ago by desouzareis.r ▴ 280
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Answer: A: HPV genes visualization on IGV
3.2 years ago by desouzareis.r ▴ 280
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Answer: A: ANNOVAR. How to prepare the database with RefSeq.hg38.gff?
3.2 years ago by desouzareis.r ▴ 280
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