Whole-genome sequence of the planarian Dugesia japonica combining Illumina and PacBio data

Advances in stem cell biology have posed the challenges in revealing the mechanistic themes underlying whole tissues and organs formation during regeneration. The planarian Dugesia japonica is an ideal model organism for the study of regeneration and stem cell biology. However, the genome resources...

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Veröffentlicht in:Genomics (San Diego, Calif.) Calif.), 2022-03, Vol.114 (2), p.110293-110293, Article 110293
Hauptverfasser: Tian, Qingnan, Guo, Qi, Guo, Yanan, Luo, Longhai, Kristiansen, Karsten, Han, Zujing, Fang, Huimin, Zhang, Shoutao
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Sprache:eng
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Zusammenfassung:Advances in stem cell biology have posed the challenges in revealing the mechanistic themes underlying whole tissues and organs formation during regeneration. The planarian Dugesia japonica is an ideal model organism for the study of regeneration and stem cell biology. However, the genome resources for this species are still limited. Here, we combined single-molecule real-time DNA sequencing platform Pacific Biosciences (PacBio) sequencing, Illumina paired-end sequencing and 10× Genomics linked reads data to obtain the whole-genome sequence of the planarian D. japonica. The final assembled D. japonica genome is 1.13G with contig N50 of 248.44 kb, and scaffold N50 of 652.52 kb. Repeat elements account for 64.92% of the genome, and 12,031 protein coding genes were annotated, of which 10,114 genes had at least one functional annotation, representing 84.07% of the total genes. We present a highly contiguous genome assembly of D. japonica. The D. japonica genome assembly, together with gene annotation and transcriptome data provide a valuable resource to investigate molecular mechanism of planarian and stem cell research. •The whole-genome sequence of the planarian D. japonica was obtained.•The final assembled D. japonica genome is 1.13G with contig N50 of 248.44 kb, and scaffold N50 of 652.52 kb.•Repeat elements account for 64.92% of the genome, and 12,031 protein coding genes were annotated.
ISSN:0888-7543
1089-8646
DOI:10.1016/j.ygeno.2022.110293