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:: Genomic Medicine Institute :: Seoul National University, College of Medicine ::

TIARA: a database for accurate analysis of multiple personal genomes based on cross-technology (NAR 2010). Reference-unbiased copy number variant analysis using CGH microarrays (NAR 2010). Discovery of common Asian copy number variants using integrated high-resolution array CGH and massively parallel DNA sequencing (NATURE Genet. 2010). A highly annotated whole-genome sequence of a Korean individual (NATURE 2009). AK1 - whole-genome sequence data. AK2 - whole-genome sequence data.

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:: Genomic Medicine Institute :: Seoul National University, College of Medicine :: | gmi.ac.kr Reviews
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TIARA: a database for accurate analysis of multiple personal genomes based on cross-technology (NAR 2010). Reference-unbiased copy number variant analysis using CGH microarrays (NAR 2010). Discovery of common Asian copy number variants using integrated high-resolution array CGH and massively parallel DNA sequencing (NATURE Genet. 2010). A highly annotated whole-genome sequence of a Korean individual (NATURE 2009). AK1 - whole-genome sequence data. AK2 - whole-genome sequence data.
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1 publications
2 download
3 informatics
4 analysis
5 asiangenomecenter
6 gendiscan
7 genome data download
8 psoma
9 acpm
10 all rights reserved
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:: Genomic Medicine Institute :: Seoul National University, College of Medicine :: | gmi.ac.kr Reviews

https://gmi.ac.kr

TIARA: a database for accurate analysis of multiple personal genomes based on cross-technology (NAR 2010). Reference-unbiased copy number variant analysis using CGH microarrays (NAR 2010). Discovery of common Asian copy number variants using integrated high-resolution array CGH and massively parallel DNA sequencing (NATURE Genet. 2010). A highly annotated whole-genome sequence of a Korean individual (NATURE 2009). AK1 - whole-genome sequence data. AK2 - whole-genome sequence data.

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:: FX - Variants caller on Cloud ::

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:: Genome Browser in GMI Database ::

Rray cgh data and high-throughput sequencing R. Human genome database on Genomic Medicine Institute ( GMI. Seoul National University College of Medicine. In this update, the variants based on human genome reference (hg19) are added. The genome browser of TIARA facilitates comparison of the genome and transcriptome sequencing results for individual humans, as well as simultaneous and efficient viewing of genomic variants from other high-throughput genome technologies. Of high-resolution CGH array data in ...

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1

:: Genomic Medicine Institute :: Seoul National University, College of Medicine ::

http://gmi.ac.kr/download/ak2_gene

Use of the data for any purpose requires approval from GMI prior to its use. Anyone who pursue using of the data should contact GMI at jeongsun@snu.ac.kr. I accept these terms and conditions. Genome and other data. AK1 - whole-genome sequence data. AK2 - whole-genome sequence data. NA10851 - whole-genome sequence data. AsianCNV - Agilent 24M aCGH data.

2

:: Genomic Medicine Institute :: Seoul National University, College of Medicine ::

http://gmi.ac.kr/publication/view/5

Dongwan Hong, Sung-Soo Park, Young Seok Ju, Sheehyun Kim, Jong-Yeon Shin, Sujung Kim, Saet-Byeol Yu, Won-Chul Lee, Seungbok Lee, Hansoo Park, Jong-Il Kim, and Jeong-Sun Seo. Genome and other data download. AK1 - whole-genome sequence data.

3

:: Genomic Medicine Institute :: Seoul National University, College of Medicine ::

http://gmi.ac.kr/about/professor

Jeong-Sun SEO M.D., Ph.D. Genomic Medicine Institute Department of Biochemistry and Molecular Biology Seoul National University College of Medicine 28 Yongon-dong, Chongno-gu, Seoul 110-799, Korea. Seoul National University College of Medicine (M.D.). Seoul National University, Biochemistry and Molecular Biology (Ph.D.). Professor, Seoul National University, Korea. Visiting Scientist, Department of Molecular Genetics, NIH, USA. Chief, Division of Molecular Medicine, Cancer Research Center, SNU, Korea.

4

:: Genomic Medicine Institute :: Seoul National University, College of Medicine ::

http://gmi.ac.kr/download

Genome and other data. AK1 - whole-genome sequence data. AK2 - whole-genome sequence data. NA10851 - whole-genome sequence data. AsianCNV - Agilent 24M aCGH data.

5

:: Genomic Medicine Institute :: Seoul National University, College of Medicine ::

http://gmi.ac.kr/download/ak1_gene

Alignment software: GSNAP, Reference sequnce: NCBI Build 36.3. SNPs: GMIAK1SNP.gff3 - Download. Indels: GMIAK1Indel.gff3 - Download. Structural Variantions: GMIAK1CNV.gff3 - Download. Genome and other data. AK1 - whole-genome sequence data. AK2 - whole-genome sequence data. NA10851 - whole-genome sequence data. AsianCNV - Agilent 24M aCGH data.

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References - Whijae Roh

http://www.whijaeroh.com/references

Andrew Futreal, Ph.D. Professor, Dept. of Genomic Medicine. The University of Texas MD Anderson Cancer Center. The University of Texas MD Anderson Cancer Center. 1901 East Road, Houston, Texas 77054. Michelle Barton, Ph.D. Professor, Dept. of Biochemistry and Molecular Biology. Dean, University of Texas Graduate School of Biomedical Sciences at Houston. Co-Director, Center for Stem Cell and Developmental Biology. The University of Texas MD Anderson Cancer Center. 6767 Bertner St. Houston, TX 77030. The U...

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http://www.stemformatics.org/project_grandiose

No in-page help for this page. Create Gene List Tutorial. Gene List View Tutorial. Gene Expression Graph Tutorial. Rohart Msc Test Tutorial. General Help and FAQ. Project Grandiose defines two reprogramming trajectories, which arrive at distinct pluripotent states: the "F-class" and embryonic stem cell (ESC)-like iPSCs. The F-class state represents reprogramming factor dependent cells, whilst the (ESC)-like iPSCs state represent reprogramming factor independent cells. Hussein, S. M. I., Puri,...Genome-wi...

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:: Genomic Medicine Institute :: Seoul National University, College of Medicine ::

TIARA: a database for accurate analysis of multiple personal genomes based on cross-technology (NAR 2010). Reference-unbiased copy number variant analysis using CGH microarrays (NAR 2010). Discovery of common Asian copy number variants using integrated high-resolution array CGH and massively parallel DNA sequencing (NATURE Genet. 2010). A highly annotated whole-genome sequence of a Korean individual (NATURE 2009). AK1 - whole-genome sequence data. AK2 - whole-genome sequence data.

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