The study of the human microbiome has dramatically expanded our understanding of the role that microbes play in health and disease. These studies have been facilitated by the development of next-generation sequencing (NGS) technologies, which are capable of generating enough sequences to cover most of the diversity present in a sample. However, capturing the full composition is still a challenge, even when estimated by the distribution of 16S rDNA sequences (Ni et al., 2013; Tamames et al., 2012). The study of transcriptomes of whole microbial communities, or metatranscriptomics, has increased exponentially in the last few years (Shakya et al., 2019; Zhang et al., 2019), and trying to analyze these kind of data has produced a new set of challenges. Thus, García-Ortega