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nhansen/README.md

I'm a staff scientist at the National Institutes of Health working to learn more about variation in the human genome. Pronouns: She/her

Popular repositories

  1. SVanalyzer SVanalyzer Public

    Tools for the analysis of structural variation in genomes

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    Shimmer is a software package for the characterization of genetic differences between two very similar samples, e.g., a tumor sample and its matched normal tissue sample.

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    Software for calling variants from next-generation sequence data.

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  4. MMBVariantCalling MMBVariantCalling Public

    Scripts and updates for running the variant pipeline described in "Variant Calling From Next Generation Sequence Data" by Nancy F. Hansen

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