Tohoku University Graduate School of Medicine briefing session (December 6, 2014)

Tohoku University Graduate School of Medicine briefing session will be held on December 6th.

For the information for the entrance exams, please click here

・Date/Time: December 6(Sat) 10:30‐12:00 (The room will be available from 10:00)
・Venue: Lecture Room 1, Building #1, Tohoku University School of Medicine

Briefing session is for those who are planning to major in Medical Science, Disability Science, Health Science, and Public Health or applying for graduate programs for next year onward.
Contents:Messages from Dean, Graduate School of Medicine, introductions of each major, presentations by graduate students (Medical Science, Disability Science, Health Science, and Public Health), financial aid, and points of attention concerning application, and Q&As.

・The time for visiting a laboratory is allocated after the end of the session.
・Please be advised that you should make a direct contact with the field you hope to visit in advance.
・Neither prior application nor participation fee is necessary.
・Since parking lot is not available, visitors are encouraged to use public transportation.

Prof. Nagasaki gives a presentation at Karolinska-Tohoku Joint Symposium on Medical Sciences. (November 8, 2014)

Title: Data management and bioinformatics of thousands Japanese whole-genome project
Symposium Name: Karolinska-Tohoku Joint Symposium on Medical Sciences
Date: 2014/Nov/8 (Sat) 15:05-15:30
Location: Tohoku Mediacl Megabank Building Meeting Room Tohoku University
Presenter: Prof. Masao Nagasaki
URL: http://www.megabank.tohoku.ac.jp/english/news/detail.php?id=829&c1=3

The 50th In Silico Megabank Research Seminar(September 26, 2014)

The 50th In Silico Megabank Research Seminar will be held on Friday, September 26.
This Time, we will be welcoming Dr. Kitano, Ibaraki University as our lecturer, and he will be speaking on “Evolution of Blood Group Genes”.

・Date/Time: September 26(Fri.) 17:00‐18:30
・Venue : Small Conference Room 2(3rd Floor), Tohoku Medical Megabank Building
・Title: Evolution of Blood Group Genes
・Lecturer: Takashi Kitano (Department of Biomolecular Functional Engineering,
College of Engineering, Ibaraki University)

*This lecture is transferable as a class in the medical research-related lecture course.

・Abstract :. Small variance in the structure of erythrocyte cell surface is categorized into groups based on the antigen-antibody reaction, and this is what we call blood groups. The antigens of ABO type blood groups are sugar chains. The base is the sugar chain of type O. The sugar chain comprised of the base with a terminal N-Acetylgalactosamine is type A and with a terminal galactose is type B. ABO type blood group genes are ones that code glycosyltransferase to link those terminal sugars. The difference in 2 amino acids above exon 7 creates the difference in the sugar attached, which in turn forms the sugar chain of type A or type B. Also, the frame shift due to single base deletion above exon 6 causes inhibition of the production of functional glycosyltransfrase, and as a consequence neither terminal sugar is attached. This is the sugar chain of type O. On the other hand, RH blood group genes are the ones that code proteins for transporters with 12 transmembrane domains, and the different types of the amino acids placed outer-membrane of these proteins are categorized in this group.
In this lecture, molecular basis and evolution of ABO and RH blood group genes are introduced.

・Organizer : Yosuke Kawai, Masao Nagasaki

Recruiting Researchers to utilize genome information from Tohoku University’s Tohoku Medical Megabank (August 8th 2014)

On August 8th 2014, we, Tohoku University’s Medical Megabank, published an allele frequency of more than 5% on known variants in order to advance the validation of our Genome Reference Panel Draft. Though variant information of more than 1% will be sold in the future, we aim to improve the verification and accuracy of our draft version. Therefore, we are proud to announce that we are accepting research proposals aimed at achieving an allele frequency of less than 1% within variants.

1.)     Joint Research related to single nucleotide polymorphism with in the
ToMMo Genome Reference Panel Draft.
2.)     Joint Research related to deleting, inserting, and copying within the
ToMMo Genome Reference Panel Draft.
3.)     Joint Research contrasting the ToMMo Genome Reference Panel Draft to
healthy people.
4.)     Joint Research involving a case-compare study on an SNP array used on
Japanese people.

For more information click on the link below:
http://www.megabank.tohoku.ac.jp/news/5710

Professor Masao Nagasaki will be giving a guest lecture at Kyushu University. (September 16,2014)

Symposium Name: in Japanese: Sin-Seimei-Kagaku Bunya Kaitaku to Super Computer “Kei”
Title:Supercomputer system and large scale cohort in Tohoku Medical Megabank Organization (in Japanese: Tohoku Medical Megabank Kikou no daikibo genome cohort to keisan inhura)
Date: 16/Sep/2014 (Tue), 14:25 to 15:10
Location: Kyushu University’s Medical facility’s Hundred Year Auditorium
Presenter: Prof. Nagasaki
Presentation Language: Japanese
URL: Official website (only in Japanese)

The 49th In Silico Megabank Research Seminar(September 12, 2014)

The 49th In Silico Megabank Research Seminar will be held on Friday, September 12.

This Time, we will be welcoming Dr. Kohda, Saitama Medical University as our lecturer, and he will be speaking on “Comprehensive Genomic Analysis on Mitochondrial Respiratory Chain Disorder”.
・Date/Time : September 12(Friday) 17:00‐18:30
・Venue : Small Conference Room 2(3rd Floor), Tohoku Medical Megabank Building
・Title : Comprehensive Genomic Analysis on Mitochondrial Respiratory Chain Disorder
・Lecturer : Masakazu Kohda(Research Center for Genomic Medicine, Saitama Medical University)

*This lecture is transferable as a class in the medical research-related lecture course.

・Abstract : Mitochondrial respiratory chain disorder (MRCD) is one of the intractable diseases and is an inborn error of metabolism with frequent incidence of 6.2 in 100,000 infants. Abnormality of various protein involved in respiratory chain complex has been revealed as a cause of MRCD; until now approximately 150 causative genes have been found. However, some part of causative genes and the mechanism of the development still remain unknown. In the research, 6 mitochondria-related genes were successfully found as new causative genes through comprehensive genomic analysis on MRCE. Furthermore, multiple genes with unknown direct relationship with MRCD were identified as causative genes for the occurrence of phenotype in patients. Data obtained in this research can contribute to the development of the foundation of genomic analysis for MRCD; thus, high usability of the findings from the data on the understanding of genes, which have been yet remained unknown, is expected.

・Organizer : Masao Nagasaki

An article of quality control software for ultra-high-throughput DNA data was published and marked as “highly accessed” article of the journal.

An article of quality control software for ultra-high-throughput DNA data was published and marked as “highly accessed” article of the journal.

Title: SUGAR: graphical user interface-based data refiner for high-throughput DNA sequencing
BMC Genomics. 2014, 15: 664 (doi: 10.1186/1471-2164-15-664)
PMID:25103311