RIKEN Integrated Sequence Analysis (RISA) System—384-Format Sequencing Pipeline with 384 Multicapillary Sequencer
Kazuhiro Shibata,Masayoshi Itoh,Katsunori Aizawa,Sumiharu Nagaoka,N Sasaki,Piero Carninci,Hideaki Konno,Jun-ichi Akiyama,K Nishi,Tokuji Kitsunai,H Tashiro,N Sumi,Yoshiyuki Ishii,S Nakamura,M Hazama,T Nishine,A Harada,R Yamamoto,H Matsumoto,Shimon Sakaguchi,T Ikegami,K Kashiwagi,S Fujiwake,K Inoue,Y Togawa +24 more
TL;DR: The RIKen high-throughput 384-format sequencing pipeline including a 384-multicapillary sequencer (the so-called RISA sequencer) was developed for the RIKEN mouse encyclopedia project and one haploid genome shotgun sequence of a higher organism can be revealed by seven RISA systems within one month.
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Abstract: The RIKEN high-throughput 384-format sequencing pipeline (RISA system) including a 384-multicapillary sequencer (the so-called RISA sequencer) was developed for the RIKEN mouse encyclopedia project. The RISA system consists of colony picking, template preparation, sequencing reaction, and the sequencing process. A novel high-throughput 384-format capillary sequencer system (RISA sequencer system) was developed for the sequencing process. This system consists of a 384-multicapillary auto sequencer (RISA sequencer), a 384-multicapillary array assembler (CAS), and a 384-multicapillary casting device. The RISA sequencer can simultaneously analyze 384 independent sequencing products. The optical system is a scanning system chosen after careful comparison with an image detection system for the simultaneous detection of the 384-capillary array. This scanning system can be used with any fluorescent-labeled sequencing reaction (chain termination reaction), including transcriptional sequencing based on RNA polymerase, which was originally developed by us, and cycle sequencing based on thermostable DNA polymerase. For long-read sequencing, 380 out of 384 sequences (99.2%) were successfully analyzed and the average read length, with more than 99% accuracy, was 654.4 bp. A single RISA sequencer can analyze 216 kb with >99% accuracy in 2.7 h (90 kb/h). For short-read sequencing to cluster the 3' end and 5' end sequencing by reading 350 bp, 384 samples can be analyzed in 1.5 h. We have also developed a RISA inoculator, RISA filtrator and densitometer, RISA plasmid preparator which can handle throughput of 40,000 samples in 17.5 h, and a high-throughput RISA thermal cycler which has four 384-well sites. The combination of these technologies allowed us to construct the RISA system consisting of 16 RISA sequencers, which can process 50,000 DNA samples per day. One haploid genome shotgun sequence of a higher organism, such as human, mouse, rat, domestic animals, and plants, can be revealed by seven RISA systems within one month.
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High Efficiency Selection of Full-length cDNA by Improved Biotinylated Cap Trapper
Piero Carninci,Arthur N. Westover,Yoko Nishiyama,Tomoya Ohsumi,Masayoshi Itoh,Sumiharu Nagaoka,Nobuya Sasaki,Yasushi Okazaki,Masami Muramatsu,Claudio Schneider,Yoshihide Hayashizaki +10 more
TL;DR: The efficiency and specificity of the new version of the protocol for cap structure biotinylation and capture of full-length cDNA is reported, which allows long cDNAs to be cloned more efficiently.
RIKEN Integrated Sequence Analysis (RISA) System—384-Format Sequencing Pipeline with 384 Multicapillary Sequencer
Kazuhiro Shibata,Masayoshi Itoh,Katsunori Aizawa,Sumiharu Nagaoka,N Sasaki,Piero Carninci,Hideaki Konno,Jun-ichi Akiyama,K Nishi,Tokuji Kitsunai,H Tashiro,N Sumi,Yoshiyuki Ishii,S Nakamura,M Hazama,T Nishine,A Harada,R Yamamoto,H Matsumoto,Shimon Sakaguchi,T Ikegami,K Kashiwagi,S Fujiwake,K Inoue,Y Togawa +24 more
TL;DR: The RIKen high-throughput 384-format sequencing pipeline including a 384-multicapillary sequencer (the so-called RISA sequencer) was developed for the RIKEN mouse encyclopedia project and one haploid genome shotgun sequence of a higher organism can be revealed by seven RISA systems within one month.
Transcriptional sequencing: A method for DNA sequencing using RNA polymerase
Nobuya Sasaki,Masaki Izawa,Masanori Watahiki,Kaori Ozawa,Takumi Tanaka,Yuko Yoneda,Shuji Matsu'ura,Piero Carninci,Masami Muramatsu,Yasushi Okazaki,Yoshihide Hayashizaki +10 more
TL;DR: This method enables us to conduct a rapid isothermal sequencing reaction in <30 min, to reduce the amount of template required, and to do PCR direct sequencing without the elimination of primers and 2'-dNTP, which disturbs the Sanger sequencing reaction.
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