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NovoGraph: building whole genome graphs from long-read-based de novo assemblies
R package for visualizing complex and multi-track 1D and 2D genomic data in GenomicRanges framework
MIP based joint inference of copy number and rearrangement state in cancer whole genome sequence data.
Utility functions to extend and optimize GenomicRanges functionality.
Simulation of Tumor Genomes -- Initiated at the 2017 NYGC-NCBI Hackathon
R-based genomics workflow management
2,562 contributions in the last year
in private repositories
Nov 1 – Nov 19
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