Fig. 4: Assembly quality evaluation of spike-in control datasets.
From: Reference-free assembly of long-read transcriptome sequencing data with RNA-Bloom2
a Recall, b false discovery rates, c F1 scores, and d redundancy were evaluated for each assembly method on spike-in control data generated from three sequencing technologies: ONT direct RNA, ONT cDNA, and PacBio CCS. The spike-in control data were extracted from a mouse dataset from the LRGASP Consortium. Source data are provided as a Source Data file.
