Coble M D, Buckleton J, Butler J M, Egeland T, Fimmers R, Gill P, Gusmão L, Guttman B, Krawczak M, Morling N, Parson W, Pinto N, Schneider P M, Sherry S T, Willuweit S, Prinz M
National Institute of Standards and Technology, Applied Genetics Group, Gaithersburg, MD, USA.
ESR, Private Bag 92021, Auckland 1142, New Zealand; National Institute of Standards and Technology, Statistical Engineering Division (Guest Researcher), Gaithersburg, MD, USA.
Forensic Sci Int Genet. 2016 Nov;25:191-197. doi: 10.1016/j.fsigen.2016.09.002. Epub 2016 Sep 4.
The use of biostatistical software programs to assist in data interpretation and calculate likelihood ratios is essential to forensic geneticists and part of the daily case work flow for both kinship and DNA identification laboratories. Previous recommendations issued by the DNA Commission of the International Society for Forensic Genetics (ISFG) covered the application of bio-statistical evaluations for STR typing results in identification and kinship cases, and this is now being expanded to provide best practices regarding validation and verification of the software required for these calculations. With larger multiplexes, more complex mixtures, and increasing requests for extended family testing, laboratories are relying more than ever on specific software solutions and sufficient validation, training and extensive documentation are of upmost importance. Here, we present recommendations for the minimum requirements to validate bio-statistical software to be used in forensic genetics. We distinguish between developmental validation and the responsibilities of the software developer or provider, and the internal validation studies to be performed by the end user. Recommendations for the software provider address, for example, the documentation of the underlying models used by the software, validation data expectations, version control, implementation and training support, as well as continuity and user notifications. For the internal validations the recommendations include: creating a validation plan, requirements for the range of samples to be tested, Standard Operating Procedure development, and internal laboratory training and education. To ensure that all laboratories have access to a wide range of samples for validation and training purposes the ISFG DNA commission encourages collaborative studies and public repositories of STR typing results.
使用生物统计软件程序协助数据解读和计算似然比,对于法医遗传学家至关重要,也是亲缘关系鉴定实验室和DNA鉴定实验室日常案件工作流程的一部分。国际法医遗传学学会(ISFG)DNA委员会此前发布的建议涵盖了生物统计学评估在鉴定和亲缘关系案件中STR分型结果的应用,目前这一范围正在扩大,以提供有关这些计算所需软件的验证和核查的最佳实践。随着更大的复合扩增、更复杂的混合样本以及对大家庭检测的需求不断增加,实验室比以往任何时候都更依赖特定的软件解决方案,充分的验证、培训和详尽的文档记录至关重要。在此,我们提出法医遗传学中用于验证生物统计软件的最低要求建议。我们区分了开发验证以及软件开发人员或供应商的职责,以及最终用户要进行的内部验证研究。针对软件供应商的建议涉及,例如,软件所使用基础模型的文档记录、验证数据期望、版本控制、实施和培训支持,以及连续性和用户通知。对于内部验证,建议包括:制定验证计划、待测试样本范围的要求、标准操作规程的制定,以及内部实验室培训和教育。为确保所有实验室都能获取用于验证和培训目的的广泛样本,ISFG DNA委员会鼓励开展合作研究以及建立STR分型结果的公共数据库。