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      Forensic Body Fluid Identification by Analysis of Multiple RNA Markers Using NanoString Technology

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          Abstract

          RNA analysis has become a reliable method of body fluid identification for forensic use. Previously, we developed a combination of four multiplex quantitative PCR (qRT-PCR) probes to discriminate four different body fluids (blood, semen, saliva, and vaginal secretion). While those makers successfully identified most body fluid samples, there were some cases of false positive and negative identification. To improve the accuracy of the identification further, we tried to use multiple markers per body fluid and adopted the NanoString nCounter system instead of a multiplex qRT-PCR system. After measuring tens of RNA markers, we evaluated the accuracy of each marker for body fluid identification. For body fluids, such as blood and semen, each body fluid-specific marker was accurate enough for perfect identification. However, for saliva and vaginal secretion, no single marker was perfect. Thus, we designed a logistic regression model with multiple markers for saliva and vaginal secretion and achieved almost perfect identification. In conclusion, the NanoString nCounter is an efficient platform for measuring multiple RNA markers per body fluid and will be useful for forensic RNA analysis.

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          Most cited references18

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          Multiplexed measurements of gene signatures in different analytes using the Nanostring nCounter™ Assay System

          Background We assessed NanoString's nCounter™ Analysis System for its ability to quantify gene expression of forty-eight genes in a single reaction with 100 ng of total RNA or an equivalent amount of tissue lysate. In the nCounter™ System, multiplexed gene expression target levels are directly detected, without enzymatic reactions, via two sequence-specific probes. The individual mRNA is captured with one mRNA target sequence-specific capture probe that is used in a post-hybridization affinity purification procedure. The second mRNA target specific-sequence and fluorescent-labeled colored coded probe is then used in the detection with the 3-component complex separated on a surface via an applied electric field followed by imaging. We evaluated reproducibility, accuracy, concordance with quantitative RT-PCR, linearity, dynamic range, and the ability of the system to assay different inputs (matched samples of total RNA from Flash Frozen (FF) and Formalin Fixed Paraffin Embedded Tissues (FFPET), and crude tissue lysates (CTL)). Findings The nCounter™ Analysis System provided data equivalent to that produced by Taqman®-based assays for genes expressed within the ranges of the calibration curves (above ~0.5 mRNA copies per human cell based on an assumption of 10 pg of total RNA per cell). System response was linear over more than two orders of magnitude with typical CVs of ~6% for concentrations above 1 fM (105 molecules per mL). Profiling the industry-standard MAQC data set yielded correlation coefficients of >0.83 for intensity values and >0.99 for measured ratios. Ninety percent of nCounter™ ratio measurements were within 1.27–1.33 fold changes of the Taqman® data (0.34–0.41 in log2 scale) for FF total RNA samples. Conclusion The nCounter™ Analysis System generated robust data for multi-gene expression signatures across three different sample preparation conditions.
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            Multi-Platform Analysis of MicroRNA Expression Measurements in RNA from Fresh Frozen and FFPE Tissues

            MicroRNAs play a role in regulating diverse biological processes and have considerable utility as molecular markers for diagnosis and monitoring of human disease. Several technologies are available commercially for measuring microRNA expression. However, cross-platform comparisons do not necessarily correlate well, making it difficult to determine which platform most closely represents the true microRNA expression level in a tissue. To address this issue, we have analyzed RNA derived from cell lines, as well as fresh frozen and formalin-fixed paraffin embedded tissues, using Affymetrix, Agilent, and Illumina microRNA arrays, NanoString counting, and Illumina Next Generation Sequencing. We compared the performance within- and between the different platforms, and then verified these results with those of quantitative PCR data. Our results demonstrate that the within-platform reproducibility for each method is consistently high and although the gene expression profiles from each platform show unique traits, comparison of genes that were commonly detectable showed that detection of microRNA transcripts was similar across multiple platforms.
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              RNA in forensic science.

              RNA analysis offers insight into diseases and mechanisms leading to death and could develop into a valuable tool for diagnosis of the cause of death in forensic pathology. Other possible applications include the determination of the age of wounds and injuries and of the post-mortem interval. The molecular identification of body fluids by analysis of cell-specific mRNA expression already represents a new technique supplementing DNA analysis in forensic cases. This review explains and discusses principles, techniques and applications by offering a complete and comprehensive overview of research results in forensic RNA work.
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                Author and article information

                Journal
                Genomics Inform
                Genomics Inform
                GNI
                Genomics & Informatics
                Korea Genome Organization
                1598-866X
                2234-0742
                December 2013
                31 December 2013
                : 11
                : 4
                : 277-281
                Affiliations
                [1 ]Medical Genomics Research Center, KRIBB, Daejeon 305-806, Korea.
                [2 ]Department of Functional Genomics, University of Science of Technology, Daejeon 305-350, Korea.
                [3 ]DNA orensic Division, Supreme Prosecutor's Office, Seoul 137-730, Korea.
                Author notes
                *Corresponding author 1: Tel: +82-2-3480-3730, Fax: +82-2-3480-3606, light@ 123456spo.go.kr
                **Corresponding author 2: Tel: +82-42-879-8116, Fax: +82-42-879-8119, kimsy@ 123456kribb.re.kr

                Jong-Lyul Park and Seong-Min Park contributed equally to this work.

                Article
                10.5808/GI.2013.11.4.277
                3897857
                787375f5-23eb-42dc-85ba-d2cc400500df
                Copyright © 2013 by the Korea Genome Organization

                It is identical to the Creative Commons Attribution Non-Commercial License ( http://creativecommons.org/licenses/by-nc/3.0/).

                History
                : 25 October 2013
                : 20 November 2013
                : 21 November 2013
                Categories
                Original Article

                Genetics
                forensic,rna,body fluids
                Genetics
                forensic, rna, body fluids

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