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Rapid DNA analysis for automated processing and interpretation of low DNA content samples
BACKGROUND: Short tandem repeat (STR) analysis of casework samples with low DNA content include those resulting from the transfer of epithelial cells from the skin to an object (e.g., cells on a water bottle, or brim of a cap), blood spatter stains, and small bone and tissue fragments. Low DNA conte...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4797129/ https://www.ncbi.nlm.nih.gov/pubmed/26998214 http://dx.doi.org/10.1186/s13323-016-0033-7 |
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author | Turingan, Rosemary S. Vasantgadkar, Sameer Palombo, Luke Hogan, Catherine Jiang, Hua Tan, Eugene Selden, Richard F. |
author_facet | Turingan, Rosemary S. Vasantgadkar, Sameer Palombo, Luke Hogan, Catherine Jiang, Hua Tan, Eugene Selden, Richard F. |
author_sort | Turingan, Rosemary S. |
collection | PubMed |
description | BACKGROUND: Short tandem repeat (STR) analysis of casework samples with low DNA content include those resulting from the transfer of epithelial cells from the skin to an object (e.g., cells on a water bottle, or brim of a cap), blood spatter stains, and small bone and tissue fragments. Low DNA content (LDC) samples are important in a wide range of settings, including disaster response teams to assist in victim identification and family reunification, military operations to identify friend or foe, criminal forensics to identify suspects and exonerate the innocent, and medical examiner and coroner offices to identify missing persons. Processing LDC samples requires experienced laboratory personnel, isolated workstations, and sophisticated equipment, requires transport time, and involves complex procedures. We present a rapid DNA analysis system designed specifically to generate STR profiles from LDC samples in field-forward settings by non-technical operators. By performing STR in the field, close to the site of collection, rapid DNA analysis has the potential to increase throughput and to provide actionable information in real time. RESULTS: A Low DNA Content BioChipSet (LDC BCS) was developed and manufactured by injection molding. It was designed to function in the fully integrated Accelerated Nuclear DNA Equipment (ANDE) instrument previously designed for analysis of buccal swab and other high DNA content samples (Investigative Genet. 4(1):1–15, 2013). The LDC BCS performs efficient DNA purification followed by microfluidic ultrafiltration of the purified DNA, maximizing the quantity of DNA available for subsequent amplification and electrophoretic separation and detection of amplified fragments. The system demonstrates accuracy, precision, resolution, signal strength, and peak height ratios appropriate for casework analysis. CONCLUSIONS: The LDC rapid DNA analysis system is effective for the generation of STR profiles from a wide range of sample types. The technology broadens the range of sample types that can be processed and minimizes the time between sample collection, sample processing and analysis, and generation of actionable intelligence. The fully integrated Expert System is capable of interpreting a wide range or sample types and input DNA quantities, allowing samples to be processed and interpreted without a technical operator. |
format | Online Article Text |
id | pubmed-4797129 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-47971292016-03-18 Rapid DNA analysis for automated processing and interpretation of low DNA content samples Turingan, Rosemary S. Vasantgadkar, Sameer Palombo, Luke Hogan, Catherine Jiang, Hua Tan, Eugene Selden, Richard F. Investig Genet Research BACKGROUND: Short tandem repeat (STR) analysis of casework samples with low DNA content include those resulting from the transfer of epithelial cells from the skin to an object (e.g., cells on a water bottle, or brim of a cap), blood spatter stains, and small bone and tissue fragments. Low DNA content (LDC) samples are important in a wide range of settings, including disaster response teams to assist in victim identification and family reunification, military operations to identify friend or foe, criminal forensics to identify suspects and exonerate the innocent, and medical examiner and coroner offices to identify missing persons. Processing LDC samples requires experienced laboratory personnel, isolated workstations, and sophisticated equipment, requires transport time, and involves complex procedures. We present a rapid DNA analysis system designed specifically to generate STR profiles from LDC samples in field-forward settings by non-technical operators. By performing STR in the field, close to the site of collection, rapid DNA analysis has the potential to increase throughput and to provide actionable information in real time. RESULTS: A Low DNA Content BioChipSet (LDC BCS) was developed and manufactured by injection molding. It was designed to function in the fully integrated Accelerated Nuclear DNA Equipment (ANDE) instrument previously designed for analysis of buccal swab and other high DNA content samples (Investigative Genet. 4(1):1–15, 2013). The LDC BCS performs efficient DNA purification followed by microfluidic ultrafiltration of the purified DNA, maximizing the quantity of DNA available for subsequent amplification and electrophoretic separation and detection of amplified fragments. The system demonstrates accuracy, precision, resolution, signal strength, and peak height ratios appropriate for casework analysis. CONCLUSIONS: The LDC rapid DNA analysis system is effective for the generation of STR profiles from a wide range of sample types. The technology broadens the range of sample types that can be processed and minimizes the time between sample collection, sample processing and analysis, and generation of actionable intelligence. The fully integrated Expert System is capable of interpreting a wide range or sample types and input DNA quantities, allowing samples to be processed and interpreted without a technical operator. BioMed Central 2016-03-17 /pmc/articles/PMC4797129/ /pubmed/26998214 http://dx.doi.org/10.1186/s13323-016-0033-7 Text en © Turingan et al. 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Turingan, Rosemary S. Vasantgadkar, Sameer Palombo, Luke Hogan, Catherine Jiang, Hua Tan, Eugene Selden, Richard F. Rapid DNA analysis for automated processing and interpretation of low DNA content samples |
title | Rapid DNA analysis for automated processing and interpretation of low DNA content samples |
title_full | Rapid DNA analysis for automated processing and interpretation of low DNA content samples |
title_fullStr | Rapid DNA analysis for automated processing and interpretation of low DNA content samples |
title_full_unstemmed | Rapid DNA analysis for automated processing and interpretation of low DNA content samples |
title_short | Rapid DNA analysis for automated processing and interpretation of low DNA content samples |
title_sort | rapid dna analysis for automated processing and interpretation of low dna content samples |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4797129/ https://www.ncbi.nlm.nih.gov/pubmed/26998214 http://dx.doi.org/10.1186/s13323-016-0033-7 |
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