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  1. Article

    Open Access

    Rare coding variants in CHRNB2 reduce the likelihood of smoking

    Human genetic studies of smoking behavior have been thus far largely limited to common variants. Studying rare coding variants has the potential to identify drug targets. We performed an exome-wide association...

    Veera M. Rajagopal, Kyoko Watanabe, Joelle Mbatchou, Ariane Ayer… in Nature Genetics (2023)

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  2. No Access

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    Short Read Map** for Exome Sequencing

    Map** short reads to the reference genome is very often the prerequisite for applications utilizing the next-generation sequencing technologies. A dozen of software tools developed for this purpose have been...

    Xueya Zhou, Suying Bao, Binbin Wang, Xuegong Zhang… in Deep Sequencing Data Analysis (2013)

  3. No Access

    Article

    Evaluation of next-generation sequencing software in map** and assembly

    Next-generation high-throughput DNA sequencing technologies have advanced progressively in sequence-based genomic research and novel biological applications with the promise of sequencing DNA at unprecedented ...

    SuYing Bao, Rui Jiang, WingKeung Kwan, BinBin Wang, Xu Ma… in Journal of Human Genetics (2011)