During the Joseon Dynasty of Korea, a reasonable investigation of the dead was well developed even before the introduction of modern forensic techniques from Western countries. Various reviews have been attempted on those investigation records currently stored in the Gyujanggak library, but an in-depth analysis has not been conducted on the extent to which the evidence mobilized at the time is valid from the perspective of modern forensic science. Therefore, we conducted a full-scale forensic review of the Gyujanggak record as an interdisciplinary study between forensic science and humanities. The case of Park Bong-Un which occurred in 1902 was investigated by Korean Empire officials who concluded that the deceased was killed by the beating of the suspect. The entire investigation of the Park Bong-Un case was described by the officials in detail, and the conclusion was made according to a credible process although various methods used in modern forensic investigation were impossible during the period.

During the Joseon Dynasty of Korea, a reasonable investigation of the dead was well developed even before the introduction of modern forensic techniques from Western countries. Various reviews have been attempted on those investigation records currently stored in the Gyujanggak library, but an in-depth analysis has not been conducted on the extent to which the evidence mobilized at the time is valid from the perspective of modern forensic science. Therefore, we conducted a full-scale forensic review of the Gyujanggak record as an interdisciplinary study between forensic science and humanities. The case of Park Bong-Un which occurred in 1902 was investigated by Korean Empire officials who concluded that the deceased was killed by the beating of the suspect. The entire investigation of the Park Bong-Un case was described by the officials in detail, and the conclusion was made according to a credible process although various methods used in modern forensic investigation were impossible during the period.

During the Joseon Dynasty of Korea, a reasonable investigation of the dead was well developed even before the introduction of modern forensic techniques from Western countries. Various reviews have been attempted on those investigation records currently stored in the Gyujanggak library, but an in-depth analysis has not been conducted on the extent to which the evidence mobilized at the time is valid from the perspective of modern forensic science. Therefore, we conducted a full-scale forensic review of the Gyujanggak record as an interdisciplinary study between forensic science and humanities. The case of Park Bong-Un which occurred in 1902 was investigated by Korean Empire officials who concluded that the deceased was killed by the beating of the suspect. The entire investigation of the Park Bong-Un case was described by the officials in detail, and the conclusion was made according to a credible process although various methods used in modern forensic investigation were impossible during the period.

During the Joseon Dynasty of Korea, a reasonable investigation of the dead was well developed even before the introduction of modern forensic techniques from Western countries. Various reviews have been attempted on those investigation records currently stored in the Gyujanggak library, but an in-depth analysis has not been conducted on the extent to which the evidence mobilized at the time is valid from the perspective of modern forensic science. Therefore, we conducted a full-scale forensic review of the Gyujanggak record as an interdisciplinary study between forensic science and humanities. The case of Park Bong-Un which occurred in 1902 was investigated by Korean Empire officials who concluded that the deceased was killed by the beating of the suspect. The entire investigation of the Park Bong-Un case was described by the officials in detail, and the conclusion was made according to a credible process although various methods used in modern forensic investigation were impossible during the period.

Background: Relatives share more genomic regions than unrelated individuals, with closer relatives sharing more regions. This concept, paired with the increased availability of highthroughput single nucleotide polymorphism (SNP) genotyping technologies, has made it feasible to measure the shared chromosomal regions between individuals to assess their level of relation to each other. However, such techniques have remained in the conceptual rather than practical stages in terms of applying measures or indices. Recently, we developed an index called “genetic distance-based index of chromosomal sharing (GD-ICS)” utilizing large-scale SNP data from Korean family samples and demonstrated its potential for practical applications in kinship determination. In the current study, we present validation results from various real cases demonstrating the utility of this method in resolving complex familial relationships where information obtained from traditional short tandem repeats (STRs) or lineage markers is inconclusive. Methods: We obtained large-scale SNP data through microarray analysis from Korean individuals involving 13 kinship cases and calculated GD-ICS values using the method described in our previous study. Based on the GD-ICS reference constructed for Korean families, each disputed kinship was evaluated and validated using a combination of traditional STRs and lineage markers. Results: The cases comprised those A) that were found to be inconclusive using the traditional approach, B) for which it was difficult to apply traditional testing methods, and C) that were more conclusively resolved using the GD-ICS method. This method has overcome the limitations faced by traditional STRs in kinship testing, particularly in a paternity case with STR mutational events and in confirming distant kinship where the individual of interest is unavailable for testing. It has also been demonstrated to be effective in identifying various relationships without specific presumptions and in confirming a lack of genetic relatedness between individuals. Conclusion This method has been proven effective in identifying familial relationships across diverse complex and practical scenarios. It is not only useful when traditional testing methods fail to provide conclusive results, but it also enhances the resolution of challenging kinship cases, which suggests its applicability in various types of practical casework.

Background: With advance of next-generation sequencing (NGS) techniques, the need for mitochondrial DNA analysis is increasing not only in the forensic area, but also in medical fields. Methods: Two commercial programs, Converge Software (CS) and Torrent Variant Caller for variant calling of NGS data, were compared with a considerable amount of sequence data of 50 samples with a homogeneous ethnicity. Results: About 2,300 variants were identified and the two programs showed about 90% of consistency. CS, a dedicated analysis program for mitochondrial DNA, showed some advantages for forensic use. By additional visual inspection, several causes of discrepancy in variant calling results were identified. Application of different notation rules for mitochondrial sequence and the minor allele frequency close to detection threshold were the two most significant reasons. Conclusion With prospective improvement of each program, researchers and practitioners should be aware of characteristics of the analysis program they use and prepare their own strategies to determine variants.

Lactase non-persistence (LNP), one of the causes of lactose intolerance, is related to lactase gene associated single nucleotide polymorphisms (SNPs). Since the frequency of LNP varies by ethnic group and country, the research to reveal the presence or absence of LNP for specific people has been conducted worldwide. However, in East Asia, the study of lactase gene associated SNPs have not been sufficiently examined so far using ancient human specimens from archaeological sites. In our study of Joseon period human remains (n=14), we successfully revealed genetic information of lactase gene associated SNPs (rs1679771596, rs41525747, rs4988236, rs4988235, rs41380347, rs869051967, rs145946881 and rs182549), further confirming that as for eight SNPs, the pre-modern Korean people had a lactase non-persistent genotype. Our report contributes to the establishment of LNP associated SNP analysis technique that can be useful in forthcoming studies on human bones and mummy samples from East Asian archaeological sites.

Because their contents would be utilized in many parts of society, medical diagnosis should be accurate and veracious especially for dead body. Autopsy records are one of the representative form of medical diagnosis determined by forensic pathologists, which are superior to the certificates for postmortem inspection in their completeness. But autopsy has its own limitation because of morphologic and biochemical changes in postmortem status and diagnostic criteria mainly based on clinical situations. Also, various diseases with only functional impairments or borderline/ambiguous changes make the forensic diagnosis difficult, for example, sudden infant death syndrome (SIDS). Even though numerous researchers with various backgrounds have been dedicated to clarifying the nature of SIDS, it seems too early to use this term in autopsy diagnosis in general. A thorough investigation of the death scene, the family dynamics, and the medical history should be guaranteed and the forensic pathologists should agree for the definition and diagnostic criteria of SIDS based on scientific knowledge.

Short tandem repeats (STRs) are the most popular markers for human identification in forensics. These markers can be easily analyzed through a multiplex polymerase chain reaction and electrophoresis and provide high discrimination power. However, in STR analysis, several atypical phenomena can be observed such as allelic dropouts, drop-ins, or imbalance, which may be due to DNA polymerase slippage or DNA degradation effects. The observed atypical STR profiles can also provide information for mixed DNA samples or chromosomal abnormalities. In this study, we report a case of mosaicism detected in routine casework of paternity testing. Hair samples from a phenotypically normal male were tested, and the result presented a typical STR profile of a female for the amelogenin gene (XX). Through chromosome analysis using peripheral blood, it was found that 45,X/46,XY mosaicism resulted in the discrepancy between the genotype and the phenotype. In addition, the amount of Y chromosome detected was particularly low in hair compared to that in blood. This study shows that mosaicism can make interpretation difficult during STR analysis and suggests that sample types and repeated analysis should be considered even for routine STR testing.

Acute myeloid leukemia (AML) is a common hematologic malignancy with high mortality and a short survival period in adults. About 10% of these cases, called therapy-related AML, are reported to be the consequence of chemotherapy or radiotherapy of previous malignancy. In a clinical setting, this is usually diagnosed by peripheral blood smear or bone marrow biopsy by assessing the proportion of blasts. However, postmortem blood samples are not suitable for smear analysis because of hemolysis. Therefore, ancillary tests for identifying leukemic infiltration or related molecular change can provide an alternative diagnostic clue for AML. The deceased had been treated for 3 years for a combined type of hepatocellular carcinoma with multiple pulmonary metastases. Treatments included the resections of primary and metastatic tumors, chemotherapy, and radiotherapy, which prevented further progression of his cancer. One year after the last treatment, he suddenly collapsed without any specific symptoms and shortly died. The microscopic examination of the autopsy samples revealed extensive extramedullary infiltration of leukemia, which was confirmed as an AML by a series of ancillary immunohistochemical staining. This case illustrates both the importance of careful hematologic observation in cancer survivors and the necessity of a detailed medical diagnosis in a medicolegal autopsy.