Abstract
AbstractNanopore sequencing enables the efficient and unbiased measurement of transcriptomes. Current methods for transcript identification and quantification rely on mapping reads to a reference genome, which precludes the study of species with a partial or missing reference or the identification of disease-specific transcripts not readily identifiable from a reference. We present RATTLE, a tool to perform reference-free reconstruction and quantification of transcripts using only Nanopore reads. Using simulated data and experimental data from isoform spike-ins, human tissues, and cell lines, we show that RATTLE accurately determines transcript sequences and their abundances, and shows good scalability with the number of transcripts.
Funder
Agencia Estatal de Investigación
Ministerio de Ciencia, Innovación y Universidades
Agència de Gestió d'Ajuts Universitaris i de Recerca
Australian Research Council
Publisher
Springer Science and Business Media LLC
Cited by
28 articles.
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