A program to write standardized tab-delimited files of tRNA-seq seed coverage and modification results.
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This program generates tabular files of tRNA-seq seed coverage and modification data that are easily manipulable by the user.
anvi-tabulate-trnaseq is part of the trnaseq-workflow, and is run following the finalization of tRNA seeds by anvi-merge-trnaseq.
This program generates a table, seeds-specific-txt, containing the specific coverage of each nucleotide position in each seed in every sample. If a nonspecific trnaseq-profile-db is also provided, this program generates a table of nonspecific coverages, seeds-non-specific-txt. The distinction between specific and nonspecific coverage is explained in the trnaseq-profile-db artifact. These coverage tables have one row per seed per sample. They have three header rows for different ways of describing tRNA nucleotide positions: canonical position name (e.g., “discriminator_1”), canonical position (e.g., “73”), and “ordinal” position relative to all the other possible positions (e.g., “95”).
anvi-tabulate-trnaseq also generates a table, modifications-txt, containing information on each predicted modification position in each seed, with one row per modification per seed per sample. This table includes four columns of position coverage counts of the four nucleotides.
All tables include taxonomic annotations of the seeds; annotations are added to the trnaseq-contigs-db by anvi-run-trna-taxonomy.
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Are you aware of resources that may help users better understand the utility of this program? Please feel free to edit this file on GitHub. If you are not sure how to do that, find the
__resources__ tag in this file to see an example.