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mpl-interactionsSliders to control matplotlib and other interactive goodies. Works in any interactive backend and even uses ipywidgets when in a Jupyter notebook
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awesome-small-molecule-mlA curated list of resources for machine learning for small-molecule drug discovery
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sr graphA simple, one-file, header-only, C++ utility for graphs, curves and histograms.
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catchA package for designing compact and comprehensive capture probe sets.
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BridgeDbThe BridgeDb Library source code
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biolink-apiAPI for linked biological knowledge
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gnparserGNparser normalises scientific names and extracts their semantic elements.
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atroposAn NGS read trimming tool that is specific, sensitive, and speedy. (production)
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unimapA EXPERIMENTAL fork of minimap2 optimized for assembly-to-reference alignment
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ntHashFast hash function for DNA sequences
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CANDOComputational Analysis of Novel Drug Opportunities
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bystroBystro genetic analysis (annotation, filtering, statistics)
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ensembl-comparaThe Ensembl Compara Perl API and SQL schema
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faster lmm dA faster lmm for GWAS. Supports GPU backend.
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ngstoolsMy own tools code for NGS data analysis (Next Generation Sequencing)
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open-cravatA modular annotation tool for genomic variants
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biskitA Python platform for Structural Bioinformatics
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trameTrame let you weave various components and technologies into a Web Application solely written in Python.
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svg plotPlot data in SVG format using C++ (header only) library .
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plasmidtronAssembling the cause of phenotypes and genotypes from NGS data
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FluentDNAFluentDNA allows you to browse sequence data of any size using a zooming visualization similar to Google Maps. You can use FluentDNA as a standalone program or as a python module for your own bioinformatics projects.
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go4bioGolang for Bioinformatics
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trase📊 A lightweight plotting library
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