Masaomi Hatakeyama, Aluri, Sirisha, Balachadran, Mathi Thumilan, Sivarajan, Sajeevan Radha, Patrignani, Andrea, Grüter, Simon, Poveda, Lucy, Rie Shimizu-Inatsugi, Baeten, John, Francoijs, Kees-Jan, Nataraja, Karaba N., Reddy, Yellodu A. Nanja, Phadnis, Shamprasad, Ravikumar, Ramapura L., Schlapbach, Ralph, Sreeman, Sheshshayee M., and Shimizu, Kentaro K.
Finger millet (Eleusine coracana (L.) Gaertn) is an important crop for food security because of its tolerance to drought, which is expected to be exacerbated by global climate changes. Nevertheless, it is often classified as an orphan/underutilized crop because of the paucity of scientific attention. Among several small millets, finger millet is considered as an excellent source of essential nutrient elements, such as iron and zinc; hence, it has potential as an alternate coarse cereal. However, high-quality genome sequence data of finger millet are currently not available. One of the major problems encountered in the genome assembly of this species was its polyploidy, which hampers genome assembly compared with a diploid genome. To overcome this problem, we sequenced its genome using diverse technologies with sufficient coverage and assembled it via a novel multiple hybrid assembly workflow that combines nextgeneration with single-molecule sequencing, followed by whole-genome optical mapping using the Bionano IrysVR system. The total number of scaffolds was 1,897 with an N50 length>2.6Mb and detection of 96% of the universal single-copy orthologs. The majority of the homeologs were assembled separately. This indicates that the proposed workflow is applicable to the assembly of other allotetraploid genomes. [ABSTRACT FROM AUTHOR]