BC Cancer Canada's Michael Smith Genome Sciences Centre
- Vancouver, BC, Canada
- http://www.bcgsc.ca/
- rwarren@bcgsc.ca
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Pinned repositories
Repositories
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tigmint
⛓ Correct misassemblies using linked AND long reads -
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pori_ipr_python
Python adapter for generating reports uploaded to IPR using the PORI platform
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xmatchview
🗻 Visualization of genome/gene sequence synteny -
LINKS
⛓ Long Interval Nucleotide K-mer Scaffolder -
RAILS
🚝 RAILS and👞 🔨 Cobbler: Assembly Improvement by Long Sequence Scaffolding/Gap-filling -
HLAminer
⛏ HLA predictions from NGS shotgun data -
SSAKE
🍶 Genome assembly with short sequence reads -
ntEdit
✏️ ultra fast and scalable genome assembly polishing -
physlr
⛓️ Construct a Physical Map from Linked Reads -
mavis
Merging, Annotation, Validation, and Illustration of Structural variants
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RNA-Bloom
🌺 lightweight transcriptome assembly for short reads and nanopore reads -
btl
🔬 Bioinformatics Technology Lab, Genome Sciences Centre -
RNA-Scoop
interactive visualization of single-cell transcriptomes
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ntHash
ntHash: recursive nucleotide hashing
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GapPredict
Character-level language model for draft genome assembly gap-filling
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abyss
🔬 Assemble large genomes using short reads -
NanoSim
Nanopore sequence read simulator
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biobloom
Create Bloom filters for a given reference and then use it to categorize sequences
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btl_bloomfilter
The BTL C/C++ Common bloom filters for bioinformatics projects, as well as any APIs created for other programming languages.
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pavfinder
🔍 Post Assembly Variants Finder -
ntJoin
🔗 Genome assembly scaffolder using minimizer graphs -
arcs
🌈 Scaffold genome sequence assemblies using linked read sequencing data -
qupath-annotation-exchange
An extension for QuPath for importing JSON annotations made in a GSC internal application
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kollector
de novo targeted gene assembly
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ntCard
Estimating k-mer coverage histogram of genomics data
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AMPlify
Attentive deep learning model for antimicrobial peptide prediction
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Terminitor
Deep Neural Network model that predicts polyadenylation sites
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ntHits
Identifying repeats in high-throughput sequencing data