Sorting reads to references with high identity

This page summarizes the projects mentioned and recommended in the original post on /r/bioinformatics

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  • snippy

    :scissors: :zap: Rapid haploid variant calling and core genome alignment

  • I would use snippy for this if there references are haploid genomes https://github.com/tseemann/snippy

  • awesome-CRISPR

    List of software/websites/databases/other stuff for genome engineering

  • That's helpful to know, actually. I recommend looking through the abundant tools for analysis of CRISPR experiments. I would guess someone out there has a tool for assessing cut efficacy from NGS/amplicon reads. https://github.com/davidliwei/awesome-CRISPR is a good place to start, and if you don't find what you need, make your own and publish it. ;)

  • InfluxDB

    Power Real-Time Data Analytics at Scale. Get real-time insights from all types of time series data with InfluxDB. Ingest, query, and analyze billions of data points in real-time with unbounded cardinality.

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NOTE: The number of mentions on this list indicates mentions on common posts plus user suggested alternatives. Hence, a higher number means a more popular project.

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