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Mapping Bacterial Functional Networks and Pathways in Escherichia Coli using Synthetic Genetic Arrays
Published on: November 12, 2012
The widespread misuse of StringTie's gene identifier tags as de facto gene symbols does not allow consistent gene
Liana Alves de Oliveira1, Gabriela Canalli Kretzschmar2, Sara Cristina Lobo-Alves1
1Pelé Pequeno Príncipe Research Institute - Av. Silva Jardim, 1632 - Água Verde, Curitiba, PR 80250-060, Brazil.
Abstract:
Current RNA sequencing techniques allow the characterization of novel genes and transcript isoforms, with StringTie being an effective and widely used tool for transcript assembly. In merge mode, StringTie assigns identifiers to putative genes, prefixed with "MSTRG" by default. These tags are sometimes used by authors as the designated name for genes or transcripts of high relevance in their work, even though they are unique and unambiguous only within the context of one analysis. In addition, when such identifiers are used, detailed genomic information is essential to identify the genes of interest clearly. In this report, we examined 161 studies that referred to a gene or transcript by its StringTie identifier in their title or abstract. Of these, only 41% provided sufficient information to clearly identify the gene(s) of interest and allow the reproducibility of the results and their comparison to further independent research. In light of this, we offer recommendations to address this issue and improve reporting standards.
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