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q2-phylogenomics's Issues

Misc TODO

Running list of miscellaneous to-do items (current list is from review of #7, edit or add new comment for additional items)

  • make dict of default params for each method

  • remove commented-out code blocks

  • add single-end mode for map reads etc

  • dereplicate redundant code between map_reads and filter

  • add unit tests for all _assemble.py methods (see #12)

  • revisit feature table construction method in consensus_sequence

  • add validation for PileUpTSVFormat, GenBankFormat

  • move Bowtie2IndexDirFmt -> DNAFASTAFormat transformer to q2-types

  • add support for GenBank format (see note in plugin_setup.py)

  • ceil_coefficient description could be clearer; maybe specify that this is the max number of non-ACGT characters as a fraction of read length.

  • ceil_coefficient should have a range specified

  • refactor test_assemble.py code to reduce duplication where possible (e.g., the consensus sequence tests)

  • determine if it makes sense to allow overlapping sample ids in the consensus sequence step (i.e., one sample giving rise to multiple different genomes) - currently this is explicitly disallowed

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