NHI Genome Studies: Mexico Govt Sept 12 Congressional hearing

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

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  1. fastp

    An ultra-fast all-in-one FASTQ preprocessor (QC/adapters/trimming/filtering/splitting/merging...)

    1) QC the data with fastp. This'll trim out adapters and toss reads that are poor quality.

  2. SaaSHub

    SaaSHub - Software Alternatives and Reviews. SaaSHub helps you find the best software and product alternatives

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  3. bowtie2

    A fast and sensitive gapped read aligner

    2) Use bowtie2 to align reads against CHM13. This will let you separate human from nonhuman (important, as human sequences are a common contaminant in many nonhuman genomes).

  4. CHM13

    The complete sequence of a human genome

    2) Use bowtie2 to align reads against CHM13. This will let you separate human from nonhuman (important, as human sequences are a common contaminant in many nonhuman genomes).

  5. kraken2

    The second version of the Kraken taxonomic sequence classification system

    3) Use Kraken2 to classify remaining reads. I'd start with the standard database.

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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