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  • fiona0302
    Junior Member
    • May 2011
    • 1

    Hello to everybody

    Hi everyone, we are from BGI of China. A brief introduction of BGI as following:

    BGI (formerly known as Beijing Genomics Institute) was founded in Beijing on Sept 9th, 1999, with the mission of supporting the development of science and technology, building strong research teams, and promoting the development of commercial scientific services.

    With a goal of excellence, high efficiency, and accuracy, BGI has successfully completed a large numerous projects. These include sequencing 1% of the human genome for the International Human Genome Project; contributing 10% to the International Human HapMap Project; carrying out research to combat SARS; being a key player in the Sino-British Chicken Genome Project; and completely sequencing the rice genome, the silkworm genome; the first Asian diploid genome, the giant panda genome, and many more. Much of this research has been published in the top international academic journals Nature and Science. In conjunction with carrying out these projects, BGI has established its own technical platforms based on large-scale genomic sequencing, efficient bioinformatics analyses and innovative genetic health care initiatives. In the course of attaining these goals, BGI has undergone a historic breakthrough from a small sequencing center in 1999 to the largest genomics institute in Asia in 2009, and become one of the leading genomics institutes in the world. At present, BGI devotes itself to applying the results of its molecular biology and genetic research to clinical practice, as well as developing their useful molecular breeding applications.


    For more information please visit: http://www.genomics.cn/en/index.php

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  • GATTACAT
    Reply to Nine Things a Sample Prep Scientist Thinks About Before Sequencing
    by GATTACAT
    Love this - good data definitely starts from good input, and poor input can only give relatively poor data. I particularly like the mention of Nanodrop/absorbance based methods for quantification. It's such a toss up if you'll get an accurate reading or what amounts to a randomly generated number, and a lot of library/sequencing related issues can be traced back to poor quant.
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  • SEQadmin2
    Nine Things a Sample Prep Scientist Thinks About Before Sequencing
    by SEQadmin2


    I’m not a sequencing expert. I’m a purification scientist who uses NGS to evaluate workflows my group develops. With this perspective, we think about the sample first and the NGS workflow second. The sequencer is an exceptionally honest reporter, but it can only report on what you give it, so whether you get clean, interpretable data from an NGS workflow is largely determined before you begin.

    Here are nine questions we think about, in roughly the order they matter, before...
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