A DB-type anvi’o artifact. This artifact is typically generated, used, and/or exported by anvi’o (and not provided by the user)..
🔙 To the main page of anvi’o programs and artifacts.
Required or used by
A tRNA-seq profile database is a profile-db variant containing tRNA seed coverage information from one or more samples.
Specific and nonspecific coverage
The coverage of tRNA seeds by tRNA-seq reads is determined differently than the coverage of contigs by metagenomic reads. Metagenomic contigs are constructed by an assembly tool and reads are assigned to contigs by a mapping tool. Reads that map to multiple contigs are randomly assigned to one contig. tRNA-seq seeds and coverages are found simultaneously by anvi-trnaseq and anvi-merge-trnaseq. Two types of coverage are tracked: specific coverage of reads unique to seeds and nonspecific coverage of reads in multiple seeds. tRNA-seq reads are often short fragments found in numerous tRNAs; random assignment of these reads would distort tRNA abundances and coverage patterns.
Separate tRNA-seq profile databases are produced for specific and nonspecific coverages. A “combined” database containing both sets of data is produced by default for convenience, allowing specific and nonspecific coverages to be compared side-by-side in the anvi-interactive interface. A “summed” database of specific + nonspecific coverage can optionally be produced. The
--nonspecific-output option of anvi-merge-trnaseq controls the production of nonspecific, combined, and summed databases.
Modifications versus SNVs
The other significant difference between a tRNA-seq profile database and a normal profile-db is that variable nucleotides are restricted to tRNA modification positions predicted from mutation signatures. Single nucleotide variants are purposefully excluded, though they can be mistaken for modifications, especially with permissive parameterization of anvi-merge-trnaseq (see that artifact for more information).
Edit this file to update this information.