An inconclusive digital audio authenticity examination: a unique case

This case report sets forth an authenticity examination of 35 encrypted, proprietary-format digital audio files containing recorded telephone conversations between two codefendants in a criminal matter. The codefendant who recorded the conversations did so on a recording system he developed; additionally, he was both a forensic audio authenticity examiner, who had published and presented in the field, and was the head of a professional audio society's writing group for authenticity standards. The authors conducted the examination of the recordings following nine laboratory steps of the peer-reviewed and published 11-step digital audio authenticity protocol. Based considerably on the codefendant's direct involvement with the development of the encrypted audio format, his experience in the field of forensic audio authenticity analysis, and the ease with which the audio files could be accessed, converted, edited in the gap areas, and reconstructed in such a way that the processes were undetected, the authors concluded that the recordings could not be scientifically authenticated through accepted forensic practices.     

激光显微切割技术与低体系扩增方法的法医学应用探索

目的建立减少DNA低体积扩增过程中产生气泡的方法。方法采用激光显微切割技术、PALM系统收集目标细胞,并在1μL～1.5μL低体积扩增样本,加入扩增液0.7μL～0.8μL。结果低体积扩增反应中的失败位点比例为2.3%,比常规反应位点时常会产生气泡导致该位点样本扩增失败且达30%以上的比例显著降低。结论低体积扩增方法可以减少或克服扩增过程中气泡的产生,提高扩增成功率。     

以太网网络接口卡MAC永久地址与MAC当前地址的检验方法综述

本文综述了检验以太网网络接口卡MAC永久地址和MAC当前地址的方法,针对不同的检验客体提出了可行的检验方法。并提出了MAC在先检验的发展方向。     

Internal Validation of Human Mitochondrial DNA Quantification Using Real‐Time PCR

The quantity of mitochondrial DNA (mtDNA) template added for amplification and subsequent dye terminator reactions is critical for obtaining quality sequence data. Validation of a human mtDNA real‐time quantitative PCR (qPCR) assay demonstrated its high degree of reproducibility and precision as well as an extremely sensitive threshold of detection (0.0001 pg/μL or approximately six human mtDNA copies/μL). A study of 35 nonprobative bone and teeth evidence samples revealed that 20 pg of mtDNA template is recommended for successful HV1 and HV2 sequence analysis; however, as little as 0.013 pg can generate a full mtDNA profile when using enhanced amplification reactions. The assay can also detect PCR inhibition and is useful for identifying samples that may benefit from re‐purification. Overall, the assay is an excellent method to quantify mtDNA and is useful for determining the best analytical approach for successful sequencing.     

实时荧光定量PCR检测羊肉制品中鼠源性成分

目的建立基于实时荧光PCR技术的肉制品中鼠源性成分的快速检测方法。方法以羊和鼠的细胞色素b基因序列设计特异性引物和Taqman荧光探针,通过特异性、灵敏性及模拟混合肉样检测实验,建立羊肉制品中鼠源性成分实时荧光定量PCR检测方法。结果该检测方法具有良好的特异性和灵敏度,在50mg羊肉和鼠肉的混合样品检测中,鼠源性成分检测限可低至1%。结论所建立的鼠源性成分检测的实时荧光定量PCR方法,为肉制品质量控制提供了有效的技术手段,弥补了利用RTi-PCR检测肉制品中鼠源性成分的技术空白。     

A Comparison Between Digital Radiography,Computed Tomography,and Magnetic Resonance in the Detection of Gunshot Residues in Burnt Tissues and Bone

The radiological search for GSR is crucial in burnt material although it has been rarely tested. In this study, thirty‐one bovine ribs were shot at near‐contact range and burnt to calcination in an oven simulating a real combustion. Computed tomography (CT) and magnetic resonance (MR) were performed before and after carbonization and compared with former analyses with DR (digital radiography); thus comparing the assistance, the radiological methods can provide in the search for GSR in fresh and burnt bone. DR demonstrated the greatest ability in the detection of metallic residues, CT showed lower abilities, while MR showed a high sensitivity only in soft tissues. Thus, DR can be considered as the most sensitive method in the detection of GSR in charred bones, whereas CT and MR demonstrated much less reliability. Nonetheless, the MR ameliorates the analysis of gunshot wounds in other types of remains with large quantities of soft tissues.     

微滴式数字PCR技术用于生物样品种属鉴定和绝对定量

目的 运用微滴式数字PCR技术进行生物样品的种属鉴定和绝对定量.方法 选择人mtDNA两个编码基因ND4和16S rRNA,设计特异性引物与探针,用人来源及常见动物样本验证种属特异性,再用重组质粒和2组共16份人来源生物检材,倍比稀释.使用微滴式数字PCR技术进行种属检验和绝对定量,验证其灵敏度和稳定性.结果 人重组质粒FAM （ND4）可进行人来源样品的检测,其检测结果与各级稀释梯度基本吻合,微滴式数字PCR技术可以检测出反应体系中低至单拷贝的DNA.结论 微滴式数字PCR技术可以进行生物样品的种属鉴定和绝对定量,并具有很高的灵敏度和特异性,可应用于日常法医物证检验.     

针对进程用户空间的电子数据取证方法研究

进程用户空间中的信息往往与特定用户的特定操作行为直接关联,对于证据链的建立意义重大.从数目繁多的用户空间数据结构中筛选出最重要的三种：进程环境块、线程环境块与虚拟地址描述符,说明其定位方法,并重点讨论其结构格式的电子数据取证特性,为内存空间电子数据取证提供了新的思路与方法.实例分析部分,则以目前广泛使用的Windows 7操作系统为应用背景,说明了所述方法的具体应用.     

数字录音真实性司法鉴定研究现状

随着数字录音设备的普及,以及音频编辑技术的大众化趋势,传统的检验方法和技术在当前数字录音真实性司法鉴定实践中面临着极大的挑战。模式识别和人工智能等领域的最新进展为数字录音真实性鉴定提供了有效的检验角度。通过分析和总结当前机器学习和模式识别等研究领域在数字录音真实性研究方面的前沿探索性成果,结合对当前录音真实性司法鉴定实践应用中的关键技术和方法的论述,分析和探讨数字录音真实性司法鉴定领域研究所面临的问题、挑战及未来发展趋势。指出专家经验判断分析技术和统计量化检验方法的协作并存是数字录音真实性鉴定的必然趋势和高效解决方案。     

Windows Surface RT tablet forensics

Small scale digital device forensics is particularly critical as a result of the mobility of these devices, leading to closer proximity to crimes as they occur when compared to computers. The Windows Surface tablet is one such device, combining tablet mobility with familiar Microsoft Windows productivity tools. This research considers the acquisition and forensic analysis of the Windows Surface RT tablet. We discuss the artifacts of both the Windows RT operating system and third-party applications. The contribution of this research is to provide a road map for the digital forensic examination of Windows Surface RT tablets.