Wang Genomics Lab

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1. doc-ANNOVAR doc-ANNOVAR Public

   Documentation for the ANNOVAR software

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2. InterVar InterVar Public

   A bioinformatics software tool for clinical interpretation of genetic variants by the 2015 ACMG-AMP guideline

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3. dragonstar2019 dragonstar2019 Public

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4. NanoCaller NanoCaller Public

   Variant calling tool for long-read sequencing data

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5. DeepMod DeepMod Public

   DeepMod: a deep-learning tool for genomic-scale, strand-sensitive and single-nucleotide based detection of DNA modifications

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6. PennCNV PennCNV Public

   Copy number vaiation detection from SNP arrays

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