Most amniote genomes are diploid and moderate in size (∼1-6 Gbp) and contain a large proportion of repetitive sequences. The development of next-generation sequencing technology, especially the emergence of high-fidelity (HiFi) long-read data, has made it feasible to resolve high-quality genome assembly for nonmodel species efficiently. However, reference genomes for squamate reptiles have lagged behind other amniote lineages. Here, we de novo assembled the first genome from the Chameleonidae family, the panther chameleon (Furcifer pardalis). We obtained telomere-to-telomere contigs using only HiFi data, reaching a contig N50 of 158.72 Mbp. The final chromosome-level assembly is 1.61 Gbp in size, and 100% of primary contigs were placed to pseudochromosomes using Hi-C interaction data. We also found that sequencing depth > 30 folds can ensure both the integrity and accuracy of the genome, whereas insufficient depth led to false increase in genome size and proportion of duplicated genes. We provide a high-quality reference genome valuable for evolutionary and ecological studies in chameleons as well as provide comparative genomic resources for squamate reptiles.
Keywords: Furcifer pardalis; chameleon genome; de novo assembly; reference genome.
© The Author(s) 2023. Published by Oxford University Press on behalf of Society for Molecular Biology and Evolution.