Singapore Database for Copy Number Variants. Singapore Genome Variation Project. Singapore Sequencing Malay Project. Singapore Sequencing Indian Project. From discovery, to functional validation, to clinical translation. Last updated 06 May 2014.
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Home | StatGen | statgen.nus.edu.sg Reviews
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Singapore Database for Copy Number Variants. Singapore Genome Variation Project. Singapore Sequencing Malay Project. Singapore Sequencing Indian Project. From discovery, to functional validation, to clinical translation. Last updated 06 May 2014.
statgen.nus.edu.sg
HapFinder
http://www.statgen.nus.edu.sg/~SGVP/software/hapfinder.html
Singapore Genome Variation Project. HapFinder: Finding common haplotype blocks in a database. There are currently three main types of program execution-. Can be used to identify the longest haplotype block of a pre-defined frequency that carries a specific allele at a focal snp. An example will be to find the longest haplotype block for allele A of the sickle cell locus (rs334) in the Hapmap YRI population. Please refer to the README for program instructions. Example Type 1 Program Execution. Java -jar h...
SSMP | StatGen
http://www.statgen.nus.edu.sg/~SSMP
Singapore Database for Copy Number Variants. Singapore Genome Variation Project. Singapore Sequencing Malay Project. Singapore Sequencing Indian Project. Attribution: Yana Harmila Haron. Target coverage of 30-fold. 100 base-pairs (bp) read length. Target insert size of between 300 and 400bp. 100 subjects (50 males and 50 females) from the Singapore Population Health Study. Please cite the following publication(s) if you are using the data in any publication:. Last updated 10 May 2012.
[Illuminus] Statisitcal Genetics Software
http://www.statgen.nus.edu.sg/~software/illuminus.html
Illuminus: A genotype calling algorithm. A zipped file containing the main codes and example dataset can be downloaded here: illuminus.tar.gz. Please refer to README in the zip file for program instructions. Please cite the following publication(s) if you are using the program in any publication. Teo YY, Inouye M, Small KS, Gwilliam R, Deloukas P, Kwiatkowski DP and Clark TG. (2007) A genotype calling algorithm for the Illumina BeadArray platform. Bioinformatics (Oxford, England).
TMRCA | StatGen
http://www.statgen.nus.edu.sg/~tmrca/tmrca.html
Singapore Database for Copy Number Variants. Singapore Genome Variation Project. Singapore Sequencing Malay Project. Singapore Sequencing Indian Project. Estimating time to the most recent common ancestor (TMRCA): comparison and application of eight methods. The supplementary document gives the command line we used for this study and can be downloaded here: Supplementary Document - TMRCA.docx. The simulated data we used can be downloaded here: simulated data.tar. Jin Zhou, Yik-Ying Teo.
SSIP | StatGen
http://www.statgen.nus.edu.sg/~SSIP
Singapore Database for Copy Number Variants. Singapore Genome Variation Project. Singapore Sequencing Malay Project. Singapore Sequencing Indian Project. Attribution: Yana Harmila Haron. Target coverage of 30-fold. 100 base-pairs (bp) read length. Target insert size of between 300 and 400bp. 38 subjects ( 12 males and 26 females) from the Singapore Population Health Study. Please cite the following publication(s) if you are using the data in any publication:. Last updated 06 May 2014.
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STAT resources for stat geeks in social sciences
STAT resources for stat geeks in social sciences. An example of using syntax highlighter:? On Monday, July 7, 2014. An example of using syntax highlighter:. Php $example = range(0, 9); foreach ($example as $value) { echo $value; }. Tutorial for installing this in Blogger. Syntax Comments in SPSS. On Sunday, November 3, 2013. There two way to write comments in SPSS: the non executed line and the in-line comment. The first, the non executed line. It1 = 1) dummy = 1 . It1 = 2) dummy = 0 . It1 = 1) dummy = 1 .
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ownCloud
OwnCloud will be updated to version 8.0.4. Please make sure that the database, the config folder and the data folder have been backed up before proceeding. To avoid timeouts with larger installations, you can instead run the following command from your installation directory:. Web services under your control.
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Center of Statistical Genetics - University of Pisa (Italy)
Via San Zeno 31. 56127 Pisa, Italy.
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Singapore Database for Copy Number Variants. Singapore Genome Variation Project. Singapore Sequencing Malay Project. Singapore Sequencing Indian Project. From discovery, to functional validation, to clinical translation. Last updated 06 May 2014.
StatGen
StatGen - Statistical Genetics Research Group at the Montreal Heart Institute and Université de Montréal. Our group is interested in the development and application of statistical genetics in the field of cardiovascular diseases and pharmacogenomics. We work in close collaboration with scientists at the Beaulieu-Saucier Pharmacogenomics Center at the Montreal Heart Institute. We also participate in productive collaborative efforts with clinicians and scientists at the Montreal Heart Institute, at the...
Center for Statistical Genetics at PSU
Nabla; About Us. News from ScienceDaily: New Tool for Improving Switchgrass. Center for Statistical Genetics has officially been approved by Pennsylvania State University Board of Trustees. Special Issue for Statistical Genomics in Clinical Trials was edited by Dr. Rongling Wu and Dr. Min Lin at Duke University in Journal of Biopharmaceutical Statistics, Volume 20. Inaugurating Symposium of the Center for Computational Biology will be held on July 19 (Monday), 2010. For a schedule, please CLICK HERE.
Center for Statistical Genetics
Center for Statistical Genetics. Nobody is logged in. From Center for Statistical Genetics. Members of the Center for Statistical Genetics. Genetic Meetings of Interest. We are a group of dedicated statistical geneticists led by Dr. Suzanne M. Leal at Baylor College of Medicine, Houston, Texas. Please visit the BCM website. To read about our research! Members of the Center for Statistical Genetics. Genetic Meetings of Interest. Identifying Genes for Mendelian Traits using Next Generation Sequence Data.
Department of Psychiatry
Psychiatric and Statistical Genetics. Psychiatric and Statistical Genetics. The completions of the Human Genome Project, and more recently the International HapMap Project, have laid the ground for revolutionary developments in human and medical genetics in the 21. Allen GUI Hongsheng 桂宏胜. Jonson YING Ding Ge. Juilian YEUNG Ming Yiu.
Statistical Genetics: Home
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