Difference between revisions of "IC4R009-Genome-2014-24578372"

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(The Background of This Project)
(The Background of This Project)
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==The Background of This Project==
 
==The Background of This Project==
 
*The researchers describe deep whole-genome sequencing of the aus rice cultivar Kasalath by using the advanced next-generation sequencing (NGS) technologies to gain a better understanding of the sequence and structural changes among highly differentiated cultivars.
 
*The researchers describe deep whole-genome sequencing of the aus rice cultivar Kasalath by using the advanced next-generation sequencing (NGS) technologies to gain a better understanding of the sequence and structural changes among highly differentiated cultivars.
 +
*the reference Nipponbare sequence is particularly useful for evolutionary and functional studies, its use for extensive analysis of genome diversity remains limited because of considerable inter- and intra-species and even intrasubspecies chromosomal rearrangements, such as insertionsanddeletions,duplications,inversions,translocations, and transpositions.
  
 
==Plant Culture & Treatment==
 
==Plant Culture & Treatment==

Revision as of 15:51, 26 June 2016

Project Title

  • Construction of Pseudomolecule Sequences of the aus Rice Cultivar Kasalath for Comparative Genomics of Asian Cultivated Rice


The Background of This Project

  • The researchers describe deep whole-genome sequencing of the aus rice cultivar Kasalath by using the advanced next-generation sequencing (NGS) technologies to gain a better understanding of the sequence and structural changes among highly differentiated cultivars.
  • the reference Nipponbare sequence is particularly useful for evolutionary and functional studies, its use for extensive analysis of genome diversity remains limited because of considerable inter- and intra-species and even intrasubspecies chromosomal rearrangements, such as insertionsanddeletions,duplications,inversions,translocations, and transpositions.

Plant Culture & Treatment

  • Total genomic DNA of Kasalath was extracted from young leaves of a singleplant by using the cetyltrimethylammonium bromide method
  • The researchers constructed DNA libraries with insert sizes of 800–1500 bp according to standard manufacturer’s protocols (http://www.454.com/; Basel, Switzerland) to generate long-read sequencesbyusing Roche454 pyrosequencing technology (GS-FLX Titanium and GS-FLXþ platforms) as described previously.
  • The researchers also constructed libraries with insert sizes of 250–400 bp according to the manufacturer’s instructions (Illumina, San Diego, CA, USA) to produce short single or paired-end reads on the Illumina GAIIx or HiSeq 2000 platforms.

Research Findings

Labs working on this Project

  • Agrogenomics Research Center, National Institute of Agrobiological Sciences, 2-1-2 Kannondai, Tsukuba, Ibaraki 305-8602, Japan *Genome Research Center, NODAI Research Institute, Tokyo University of Agriculture, 1-1-1 Sakuragaoka, Setagaya, Tokyo 156-8502, Japan
  • Department of Bioscience, Faculty of Applied Bioscience,Tokyo University of Agriculture, 1-1-1 Sakuragaoka, Setagaya, Tokyo 156-8502, Japan.


Corresponding Author

  • jzwu@affrc.go.jp
  • Tel. þ81 29-838-6148. Fax. þ81 29-838-6028.