RIKEN integrated sequence analysis (RISA) system-384-format sequencing pipeline with 384 multicapillary sequencer

被引:50
作者
Shibata, K
Itoh, M
Aizawa, K
Nagaoka, S
Sasaki, N
Carninci, P
Konno, H
Akiyama, J
Nishi, K
Kitsunai, T
Tashiro, H
Itoh, M
Sumi, N
Ishii, Y
Nakamura, S
Hazama, M
Nishine, T
Harada, A
Yamamoto, R
Matsumoto, H
Sakaguchi, S
Ikegami, T
Kashiwagi, K
Fujiwake, S
Inoue, K
Togawa, Y
Izawa, M
Ohara, E
Watahiki, M
Yoneda, Y
Ishikawa, T
Ozawa, K
Tanaka, T
Matsuura, S
Kawai, J
Okazaki, Y
Muramatsu, M
Inoue, Y
Kira, A
Hayashizaki, Y [1 ]
机构
[1] RIKEN, Genome Explorat Res Grp, Tsukuba, Ibaraki 3000074, Japan
[2] RIKEN, GSC, Tsukuba, Ibaraki 3000074, Japan
[3] RIKEN, Genome Sci Lab, Tsukuba, Ibaraki 3000074, Japan
[4] Japan Sci & Technol Corp, CREST, Tsukuba Inst, Tsukuba, Ibaraki 3000074, Japan
[5] RIKEN, Adv Engn Ctr, Wako, Saitama 35110198, Japan
[6] Univ Tsukuba, Sch Med, Tsukuba, Ibaraki 3058575, Japan
[7] Nippon Gene Co Ltd, Res & Dev, Toyama 9300834, Japan
[8] Wako Pure Chem Ind Ltd, Osaka Res Labs, Amagasaki, Hyogo 6610963, Japan
[9] RIKEN, Harima Inst, Sayo, Hyougo 6795148, Japan
[10] RIKEN, Wako, Saitama 3510198, Japan
关键词
D O I
10.1101/gr.152600
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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.
引用
收藏
页码:1757 / 1771
页数:15
相关论文
共 16 条
[1]  
Carninci P, 1999, METHOD ENZYMOL, V303, P19
[2]   Thermostabilization and thermoactivation of thermolabile enzymes by trehalose and its application for the synthesis of full length cDNA [J].
Carninci, P ;
Nishiyama, Y ;
Westover, A ;
Itoh, M ;
Nagaoka, S ;
Sasaki, N ;
Okazaki, Y ;
Muramatsu, M ;
Hayashizaki, Y .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (02) :520-524
[3]   High-efficiency full-length cDNA cloning by biotinylated CAP trapper [J].
Carninci, P ;
Kvam, C ;
Kitamura, A ;
Ohsumi, T ;
Okazaki, Y ;
Itoh, M ;
Kamiya, M ;
Shibata, K ;
Sasaki, N ;
Izawa, M ;
Muramatsu, M ;
Hayashizaki, Y ;
Schneider, C .
GENOMICS, 1996, 37 (03) :327-336
[4]  
Carninci P, 1997, DNA Res, V4, P61, DOI 10.1093/dnares/4.1.61
[5]  
Itoh M, 1999, GENOME RES, V9, P463
[6]   Simple and rapid preparation of plasmid template by a filtration method using microtiter filter plates [J].
Itoh, M ;
Carninci, P ;
Nagaoka, S ;
Sasaki, N ;
Okazaki, Y ;
Ohsumi, T ;
Muramatsu, M ;
Hayashizaki, Y .
NUCLEIC ACIDS RESEARCH, 1997, 25 (06) :1315-1316
[7]   Recognition sites of 3′-OH group by T7 RNA polymerase and its application to transcriptional sequencing [J].
Izawa, M ;
Sasaki, N ;
Watahiki, M ;
Ohara, E ;
Yoneda, Y ;
Muramatsu, M ;
Okazaki, Y ;
Hayashizaki, Y .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (23) :14242-14246
[8]   MULTIPLE-SHEATHFLOW CAPILLARY ARRAY DNA ANALYZER [J].
KAMBARA, H ;
TAKAHASHI, S .
NATURE, 1993, 361 (6412) :565-566
[9]   CAPILLARY ARRAY ELECTROPHORESIS - AN APPROACH TO HIGH-SPEED, HIGH-THROUGHPUT DNA SEQUENCING [J].
MATHIES, RA ;
HUANG, XC .
NATURE, 1992, 359 (6391) :167-169
[10]   Transcriptional sequencing: A method for DNA sequencing using RNA polymerase [J].
Sasaki, N ;
Izawa, M ;
Watahiki, M ;
Ozawa, K ;
Tanaka, T ;
Yoneda, Y ;
Matsuura, S ;
Carninci, P ;
Muramatsu, M ;
Okazaki, Y ;
Hayashizaki, Y .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (07) :3455-3460