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Comment: C: Understanding TCGA somatic mutation files
4.0 years ago by j.lunger18 ▴ 30
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Comment: C: bcftools merge single-sample vcf files
4.0 years ago by j.lunger18 ▴ 30
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Comment: C: gnomAD reports variants with "NA" allele count and allele frequency
4.0 years ago by j.lunger18 ▴ 30
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1.2k
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Comment: C: snpEff killed while reading genome version
4.0 years ago by j.lunger18 ▴ 30
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3.4k
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Comment: C: Fix or remove format tag in .vcf file
4.0 years ago by j.lunger18 ▴ 30
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1.8k
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Comment: C: Merge vcf files with bcftools
4.0 years ago by j.lunger18 ▴ 30
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958
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Comment: C: MD5 not the same between contig and reference; both Unified Genotyper and Haplot
4.1 years ago by j.lunger18 ▴ 30
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1.6k
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Comment: C: R Package for Visualizing SNVs from "sites only" VCF (population variants)
4.1 years ago by j.lunger18 ▴ 30
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1.6k
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Comment: C: R Package for Visualizing SNVs from "sites only" VCF (population variants)
4.1 years ago by j.lunger18 ▴ 30
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1.6k
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Comment: C: R Package for Visualizing SNVs from "sites only" VCF (population variants)
4.1 years ago by j.lunger18 ▴ 30
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1
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1.6k
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Comment: C: R Package for Visualizing SNVs from "sites only" VCF (population variants)
4.1 years ago by j.lunger18 ▴ 30
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967
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Comment: C: GENCODE and untranslated regions
4.4 years ago by j.lunger18 ▴ 30
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1.8k
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Comment: C: Extract variants from genomic range from gnomAD GRCh38
4.5 years ago by j.lunger18 ▴ 30
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2.8k
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Comment: C: extracting info field from VCF using vcfr
4.5 years ago by j.lunger18 ▴ 30
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