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1.
J Forensic Sci ; 55(3): 706-14, 2010 May.
Article in English | MEDLINE | ID: mdl-20345792

ABSTRACT

Automated platforms used for forensic casework sample DNA extraction need to be versatile to accommodate a wide variety of sample types, thus protocols frequently need modification. In this study, DNA IQ methods previously developed for the Biomek 2000 Automation Workstation were adapted for the Teleshake Unit using normal volumes and all deepwell extraction, and a large volume DNA IQ method developed. DNA purification without detectable contamination of adjacent reagent blanks is reported in the extraction of tissue samples containing several micrograms of DNA. Sensitivity and contamination studies demonstrated similar performance with the manual organic extraction method for bloodstain dilution samples. Mock casework samples demonstrated the effectiveness of the Teleshake and Teleshake large volume methods. Because of the performance and increased versatility of the DNA IQ extraction with these modifications, the Teleshake Unit has been implemented in both normal and large volume automated DNA extractions at the Virginia Department of Forensic Science.


Subject(s)
DNA/isolation & purification , Forensic Genetics/instrumentation , Robotics , Automation, Laboratory , Blood Stains , Bone and Bones/pathology , Brain/pathology , Humans , Liver/pathology , Mouth Mucosa/pathology , Muscle, Skeletal/pathology , Myocardium/pathology , Polymerase Chain Reaction , Semen/chemistry , Tandem Repeat Sequences
2.
Forensic Sci Int Genet ; 3(4): 242-50, 2009 Sep.
Article in English | MEDLINE | ID: mdl-19647709

ABSTRACT

Fired cartridge cases are a common type of evidence found at crime scenes. However, due to the high chamber temperatures and touch nature of this evidence, DNA testing is not commonly sought because it is believed DNA is only present in low levels, whether it is due to initial low levels of DNA and/or DNA degradation from the heat or inhibition of the PCR reaction. Moreover, very few laboratories report STR typing success with fired cases. This study focused on obtaining STR profiles from fired cartridge cases using the AmpFlSTR MiniFiler kit, which is designed to amplify DNA from low level, inhibited, and degraded samples. Comparisons to other STR amplification kits were also conducted. In attempt to simulate casework, random individuals loaded cartridges into a firearm. DNA was recovered from the fired cartridge cases using the double swab technique and extracted using an automated large volume DNA IQ method. Initially, testing focused on known shedders handling cartridges for 30s prior to firing. A significantly greater number of alleles was obtained following amplification with the MiniFiler kit versus the PowerPlex 16 BIO kit. No alleles were observed using the Identifiler kit. In an attempt to better simulate casework, a random selection of laboratory personnel handled shotshells for as long as needed to load and fire the weapon. In this mock sample study, the MiniFiler kit successfully amplified an average of 22% of expected alleles from DNA recovered from shotshell cases versus the PowerPlex 16 BIO kit where an average of 7% of alleles were observed. However, the total number of alleles obtained from the two kits was not significantly different. The quality of the DNA obtained from fired cases was studied with evidence of inhibition in at least 11% of shotshell case samples. After swabbing the head and the hull of three shotshell cases separately, a significantly greater number of alleles was obtained from the hull as opposed to the head of the fired shotshell case. In addition, after firing, various internal firearm surfaces were swabbed, including the chamber of barrel, ejection port, and breechface, in an attempt to obtain amplifiable DNA. DNA was obtained from the chamber of the barrel and was amplifiable using the MiniFiler kit, although mixtures were obtained with extensive drop-in and drop-out making this analysis unlikely to aid an investigation.


Subject(s)
DNA/isolation & purification , Firearms , Forensic Medicine/instrumentation , Microsatellite Repeats , Specimen Handling/instrumentation , Alleles , DNA/genetics , DNA Fingerprinting/instrumentation , Humans , Nucleic Acid Amplification Techniques/instrumentation , Polymerase Chain Reaction/instrumentation , Reagent Kits, Diagnostic
3.
Anal Chem ; 81(15): 6089-95, 2009 Aug 01.
Article in English | MEDLINE | ID: mdl-19591449

ABSTRACT

Forensic DNA analysis of samples obtained from sexual assault evidence relies on separation of male and female components of the recovered genetic material. The conventional separation method used by crime laboratories, differential extraction (DE), is one of the most time-consuming sample preparation steps, requires extensive sample handling, is difficult to automate, and often results in inefficient separation of female DNA from the male sample components. To circumvent conventional DE, acoustic differential extraction (ADE) analysis was developed on a microfluidic device. The ADE method relies on acoustic trapping of sperm cells in the presence of epithelial cell lysate (which is unretained), and laminar flow valving to direct the male and female fractions to separate outlets. Following the separation of sperm from epithelial cell lysate, DNA extraction, quantitation, amplification, and separation were performed using conventional laboratory methods. The results show that highly purified male and female fractions can be obtained with the ADE microdevice from mock sexual assault samples in 14 min. ADE analysis provides the potential to significantly alter the means by which sexual assault evidence is processed in crime laboratories.


Subject(s)
DNA Fingerprinting , DNA/analysis , Forensic Medicine , Microfluidic Analytical Techniques , Sex Offenses , Specimen Handling , Cell Separation , Epithelial Cells/cytology , Female , Humans , Male , Semen/chemistry , Semen/cytology
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