计算机科学
数据挖掘
缺少数据
大数据
数据分析
杠杆(统计)
生物制造
数据科学
机器学习
生物
遗传学
作者
Stephen Goldrick,Viktor Sandner,Matthew Cheeks,Richard Turner,Suzanne S. Farid,Graham A. McCreath,Jarka Glassey
标识
DOI:10.1002/biot.201800684
摘要
Multivariate data analysis (MVDA) is a highly valuable and significantly underutilized resource in biomanufacturing. It offers the opportunity to enhance understanding and leverage useful information from complex high-dimensional data sets, recorded throughout all stages of therapeutic drug manufacture. To help standardize the application and promote this resource within the biopharmaceutical industry, this paper outlines a novel MVDA methodology describing the necessary steps for efficient and effective data analysis. The MVDA methodology is followed to solve two case studies: a "small data" and a "big data" challenge. In the "small data" example, a large-scale data set is compared to data from a scale-down model. This methodology enables a new quantitative metric for equivalence to be established by combining a two one-sided test with principal component analysis. In the "big data" example, this methodology enables accurate predictions of critical missing data essential to a cloning study performed in the ambr15 system. These predictions are generated by exploiting the underlying relationship between the off-line missing values and the on-line measurements through the generation of a partial least squares model. In summary, the proposed MVDA methodology highlights the importance of data pre-processing, restructuring, and visualization during data analytics to solve complex biopharmaceutical challenges.
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