Table 1.

Details on each of the assemblies used in this study

NameVersionRegionLineage nameBreedingLengthScaffold N50AT-richnessGenesBUSCO scoreTechnologyLevelBioSampleReference
OkinawaOKI2018_I69_1.0Okinawa, Ryūkyū archipelagoOkinawaLaboratory64,281,56517,092,47659%17,29164%Nanopore + Illumina + HiCChromosomalSAMEA7282646Bliznina et al. 2021
KumeKUM-M3-7fKume, Ryūkyū archipelagoOkinawaWild64,653,5742,969,71959%16,85266%NanoporeScaffoldSAMEA111279290This paper
OsakaOSKA2016v1.9Honshū, Japan inland seaOsakaLaboratory56,625,16215,521,22758%15,72063%PacBio + IlluminaChromosomalSAMD00227923Wang et al. 2020a; this paper
AomoriAOM-5-5fHonshū, Japan, northeast Pacific coastOsakaWild56,753,7846,419,76359%15,22465%NanoporeScaffoldSAMEA111279288This paper
BarcelonaBar2_p4Spain, Mediterranean sea coastBarcelonaLaboratory55,793,43713,545,85760%14,27264%Nanopore + Illumina + HiCChromosomalSAMEA111279286This paper
BergenOdB3Norway, north Atlantic coastBarcelonaLaboratory70,471,451395,38757%17,11360%SangerScaffoldSAMEA2272014Denoeud et al. 2010

[i] (Name) Name of the genome reflecting provenance; (version) character string uniquely identifying the used version of the assembly file; (region) where the animal or the founders of its laboratory line was isolated; (breeding) wild isolate or laboratory culture line; (length) assembly sequence length in base pairs; (scaffold N50) half of the genome is covered by scaffolds of at least this length; (AT richness) a percentage of A's and T's in the sequence; (genes) number of genes in the annotation used in this study; (BUSCO score) detected percentage of the metazoan set of Benchmark Unique Single-Copy Orthologs; (technology) sequencing and assembly technologies used; (level) chromosomal or scaffold; (BioSample) identifier in the DDBJ, EBI, and NCBI databases; and (reference) peer-reviewed manuscripts describing the already published genome sequences.