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1. WES WES Public

   Whole Exome Sequencing Workflow

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2. SequencingDepth SequencingDepth Public

   For a better interpretation of variants, evidence-based databases, such as ClinVar, compile data on the presumed relationships between variants and phenotypes. In this study, we aimed to analyze th…

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3. 1000GenomesComp 1000GenomesComp Public

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4. picard picard Public

   Forked from broadinstitute/picard

   A set of tools (in Java) for working with next generation sequencing data in the BAM (http://samtools.github.io/hts-specs) format.

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5. DepthVariation DepthVariation Public

   Scripst used in the article

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6. mahalanobisDist mahalanobisDist Public

   Mahalanobis distance between two groups

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