BC Cancer Canada's Michael Smith Genome Sciences Centre

:microscope: Assemble large genomes using short reads

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Nanopore sequence read simulator

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Fast hash function for DNA/RNA sequences

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🌈Scaffold genome sequence assemblies using linked or long read sequencing data

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⛓ Long Interval Nucleotide K-mer Scaffolder

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✏️ Genome assembly polishing & SNV detection

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Merging, Annotation, Validation, and Illustration of Structural variants

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Estimating k-mer coverage histogram of genomics data

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:hibiscus: reference-free transcriptome assembly for short and long reads

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Create Bloom filters for a given reference and then use it to categorize sequences

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