AI Article Synopsis

  • Contiguous genome assemblies are crucial for understanding the genetic makeup of organisms, but creating them in molluscs is tough due to large genomes, genetic variation, and repetitive DNA.
  • The first genome assembly for a threatened species of freshwater mussel was produced but was fragmented because it used short-read sequencing.
  • An improved genome assembly was achieved by combining long-read and short-read sequencing, resulting in a comprehensive assembly with over 48,000 predicted protein-coding genes, aiding in the study and conservation of this species.

Article Abstract

Contiguous assemblies are fundamental to deciphering the composition of extant genomes. In molluscs, this is considerably challenging owing to the large size of their genomes, heterozygosity, and widespread repetitive content. Consequently, long-read sequencing technologies are fundamental for high contiguity and quality. The first genome assembly of (Linnaeus, 1758) (Mollusca: Bivalvia: Unionida), a culturally relevant, widespread, and highly threatened species of freshwater mussels, was recently generated. However, the resulting genome is highly fragmented since the assembly relied on short-read approaches. Here, an improved reference genome assembly was generated using a combination of PacBio CLR long reads and Illumina paired-end short reads. This genome assembly is 2.4 Gb long, organized into 1,700 scaffolds with a contig N50 length of 3.4 Mbp. The gene prediction resulted in 48,314 protein-coding genes. Our new assembly is a substantial improvement and an essential resource for studying this species' unique biological and evolutionary features, helping promote its conservation.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10189783PMC
http://dx.doi.org/10.46471/gigabyte.81DOI Listing

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