P035
A Chromosomal Genomics Approach to Assess and Validate the Desi and Kabuli Draft Chickpea Genome Assemblies

Date: Monday, January 13, 2014
Room: Grand Exhibit Hall
Pradeep Ruperao , University of Western Australia, Brisbane, Australia
Philipp Emanuel Bayer , University of Queensland, Brisbane, Australia
Kenneth Chan , University of Queensland, Brisbane, Australia
Sarwar Azam , ICRISAT, Hyderabad, India
Miroslava Havránková , Institute of Experimental Botany, Olomouc, Czech Republic
Satomi Hayashi , University of Queensland, Brisbane, Australia
Jana Cizkova , Institute of Experimental Botany, Olomouc, Czech Republic
Rachit K Saxena , ICRISAT, Patancheru, India
Hana Simkova , Institute of Experimental Botany, Olomouc, Czech Republic
Chi Song , BGI, China
Jan Vrana , Institute of Experimental Botany, Olomouc, Czech Republic
Annapurna Chitikineni , ICRISAT, Hyderabad, India
Pooran M. Gaur , ICRISAT, Hyderabad, India
Teresa Millan , University of Cordoba, Cordoba, Spain
Karam Singh , The University of Western Australia, CRAWLEY, Australia
Bunyamin Taran , University of Saskatchewan, Saskatoon, SK, Canada
Jun Wang , BGI, Shenzhen, China
Jacqueline Batley , University of Queensland, Brisbane, Australia
Jaroslav Doležel , Institute of Experimental Botany, Olomouc, Czech Republic
Rajeev Varshney , ICRISAT, Hyderabad, India
David Edwards , University of Queensland, Brisbane, Australia
The ability to isolate individual chromosomes combined with next generation sequencing permits the validation of genome assemblies at the chromosome level. We demonstrate this approach by the assessment of the recently published chickpea kabuli and desi genomes. While previous genetic analysis suggests that these genomes should be very similar, a comparison of their published assemblies highlights significant differences. Our chromosomal genomics analysis highlights regions that appear to have been mis-assembled in the kabuli genome and identifies large scale mis-assembly in the draft desi genome. The integration of chromosomal genomics with skimGBS based genome assembly tools has the potential to significantly improve genome assemblies. The approach could be applied both for new genome assemblies as well as published assemblies, and complements currently applied genome assembly strategies.
Handouts
  • PAG_poster_Chickpea_v4_PE.pdf (504.0 kB)