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Our company, as a contract research organization, undertakes clinical trial PGx analysis to enhance the efficiency of drug development and improve efficacy and safety. We provide support at all stages of analysis, including sample size estimation through power simulation based on genetic statistics, preparation of statistical analysis plans and figure layouts, and creation of informed consent forms and documents for participants. Additionally, we are well-versed in the ethics, laws, enforcement orders, regulations, and guidelines related to clinical trial PGx analysis. Based on established standard operating procedures, our experts with over 10 years of analytical experience serve as statistical analysis leaders to deliver high-quality analytical results. Please feel free to contact us if you have any requests. *For more details, please download the PDF or feel free to reach out to us.*
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Free membership registrationIn recent years, our company has focused on cancer genome data analysis, supporting customers in various ways, from basic analyses such as SNV/indel mutation detection and annotation to advanced analyses including copy number variation analysis, structural variation analysis, mutational signature analysis, neoantigen discovery, and driver mutation exploration. We have also prepared analysis pipelines and standard operating procedures for the exploration of therapeutic targets and biomarkers through cancer genome analysis, and we provide support for clinical trial operations using NGS data for pharmaceutical companies. Please feel free to contact us if you have any requests. [Analysis and Development Content] ■ Basic Analysis ■ Environmental Setup and Research Investigation ■ Copy Number Variation Analysis, etc. *For more details, please download the PDF or feel free to contact us.
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Free membership registrationWe offer online lectures on genetic statistics. Due to the online format, there is a high degree of flexibility in scheduling, and since the lectures are conducted live rather than recorded, you can ask the instructor questions on the spot, which deepens your understanding. We provide two types of sessions: a "lecture" type for listening and a "workshop" type for hands-on exercises using simulation data. Please feel free to contact us if you have any requests. 【What you can learn】 ■ You will be able to pick up keywords in genome research. ■ You will understand how to utilize the Biobank Japan Database. ■ You will be able to plan genome research. *For more details, please download the PDF or feel free to contact us.
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