2016
DOI: 10.1016/j.legalmed.2016.08.004
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Evaluation of a blood-specific DNA methylated region and trial for allele-specific blood identification from mixed body fluid DNA

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Cited by 17 publications
(7 citation statements)
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“…We then analyzed these regions using DNA from saliva (n = 12), blood (n = 9), semen (n = 9), and vaginal swab (n = 9) samples, which were not included in the pooled samples used for the genome-wide analysis. We used 2 or 5 µL of approximately 20 µL of the eluate after bisulfite treatment of 20 ng for PCR amplification, as we previously could detect specific methylation of semen and blood CpG markers using the same amount in bisulfite PCR-based methods [15,16,22]. As a result of MPS-based bisulfite sequencing, we obtained more than 1000 mapped reads for each sample except one vaginal sample.…”
Section: Searching For Saliva-specific Cpgs In Each Regionmentioning
confidence: 99%
See 1 more Smart Citation
“…We then analyzed these regions using DNA from saliva (n = 12), blood (n = 9), semen (n = 9), and vaginal swab (n = 9) samples, which were not included in the pooled samples used for the genome-wide analysis. We used 2 or 5 µL of approximately 20 µL of the eluate after bisulfite treatment of 20 ng for PCR amplification, as we previously could detect specific methylation of semen and blood CpG markers using the same amount in bisulfite PCR-based methods [15,16,22]. As a result of MPS-based bisulfite sequencing, we obtained more than 1000 mapped reads for each sample except one vaginal sample.…”
Section: Searching For Saliva-specific Cpgs In Each Regionmentioning
confidence: 99%
“…Because the differences in methylation ratios of saliva CpG markers are moderate between the target and other body fluids, the presence of a large amount of non-saliva DNA can reduce these ratios to background levels. To overcome the same potential problem with a blood methylation marker, we previously demonstrated a strategy for mixture analysis using blood-specific methylated CpGs and their neighboring single nucleotide polymorphism (SNP) [15]. This method, herein called individual-specific body fluid identification, analyzes the methylation status of CpGs and the allelic patterns of nearby SNPs by cloning-based bisulfite sequencing to detect each body fluid-specific methylation status in the target person's DNA (Fig.…”
Section: Introductionmentioning
confidence: 99%
“…One of the main tasks of forensic odontology is the identification of unidentified human remains using dental treatment marks (dental prosthesis and filling, etc) 1‐5 . Other scientific methods for body identification include DNA typing and fingerprinting 6‐11 . Forensic dental identification is not only effective for recently unidentified human remains but is also useful when mass disasters occur and cause numerous deaths.…”
Section: Introductionmentioning
confidence: 99%
“…[1][2][3][4][5] Other scientific methods for body identification include DNA typing and fingerprinting. [6][7][8][9][10][11] Forensic dental identification is not only effective for recently unidentified human remains but is also useful when mass disasters occur and cause numerous deaths. Therefore, the Disaster Victim Identification (DVI) team has been organized to promptly respond to disasters in various parts of the world.…”
Section: Introductionmentioning
confidence: 99%
“…However, in most of the studies performed previously 6 8 , 10 17 , 19 , 20 , the research object has been limited to blood samples. DNA methylation profiles can differ depending on the cell type from which the DNA is derived 25 27 . Therefore, an age prediction model established from blood DNA may not be applicable for DNA derived from other biological fluids.…”
Section: Introductionmentioning
confidence: 99%