Evidence map›Paper›PMID 37399646›Full record

ArticleForensic science international. Genetics2023

Differentiation of vaginal cells from epidermal cells using morphological and autofluorescence properties: Implications for sexual assault casework involving digital penetration.

Sarah Ingram, Arianna DeCorte, Amanda Elswick Gentry, M Katherine Philpott, Taylor Moldenhauer, Sonja Stadler, Cory Steinberg, Jonathan Millman, Christopher J Ehrhardt

Open access · greenAbstract read
In one paragraph

Article in Forensic science international. Genetics, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.9field-weighted citation impact, top 25% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed, 6 citations in OpenAlex.

  1. Article
  2. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors at 2 institutions in 2 countries.

Sarah IngramDepartment of Forensic Science, Virginia Commonwealth University, Richmond, VA 23284, USA.
Arianna DeCorteDepartment of Forensic Science, Virginia Commonwealth University, Richmond, VA 23284, USA.
Amanda Elswick GentryVirginia Institute for Psychiatric and Behavioral Genetics, Department of Psychiatry, Virginia Commonwealth University, Richmond, VA 23284, USA.
M Katherine PhilpottDepartment of Forensic Science, Virginia Commonwealth University, Richmond, VA 23284, USA.
Taylor MoldenhauerDepartment of Forensic Science, Virginia Commonwealth University, Richmond, VA 23284, USA.
Sonja StadlerCentre of Forensic Sciences, 70 Foster Drive, Sault Ste. Marie, Ontario, P6A 6V3, Canada.
Cory SteinbergCentre of Forensic Sciences, 70 Foster Drive, Sault Ste. Marie, Ontario, P6A 6V3, Canada.
Jonathan MillmanCentre of Forensic Sciences, 25 Morton Shulman Avenue, Toronto, Ontario M3M 0B1, Canada.
Christopher J EhrhardtDepartment of Forensic Science, Virginia Commonwealth University, Richmond, VA 23284, USA. Electronic address: cehrhardt@vcu.edu.
Virginia Commonwealth University · USOntario Forest Research Institute · CA

Funding

Virus Vector Shared ResourceP30CA016059 · NCI · VIRGINIA COMMONWEALTH UNIVERSITY · PI Keri R Maher · 1985 to 2026
$51.0M
NCI NIH HHS P30 CA016059
6 · The paper itself

Abstract

Analysis of DNA mixtures from sexual assault evidence is an ongoing challenge for DNA casework laboratories. To assist the forensic scientist address source and activity level propositions there is a significant need for new techniques that can provide information as to the source of DNA, particularly for sexual assault samples that do not involve semen. The goal of this study was to develop a new biological signature system that provides additional probative value to samples comprised of mixtures of epidermal and vaginal cells, as may be observed in cases involving digital penetration. Signatures were based on morphological and autofluorescence properties of individual cells collected through Imaging Flow Cytometry (IFC). Comparisons to reference cell populations from vaginal tissue and epidermal cells collected from hands showed strong multivariate differences across > 80 cellular measurements. These differences were used to build a predictive framework for classifying unknown cell populations as originating from epithelial cells associated with digital penetration or epidermal tissue. As part of the classification scheme, posterior probabilities of specific tissue group membership were calculated for each cell, along with multivariate similarity to that tissue type. We tested this approach on cell populations from reference tissue as well as mock casework samples involving hand swabbings following digital vaginal penetration. Many more cells classifying as non-epidermal tissue were detected in digital penetration hand swab samples than control hand swabbings. Minimum interpretation thresholds were developed to minimize false positives; these thresholds were also effective when screening licked hands, indicating the potential utility of this method for a variety of biological mixture types and depositional events relevant to forensic casework. Results showed that samples collected subsequent to digital penetration possessed markedly higher numbers of cells classifying as vaginal tissue as well as higher posterior probabilities for vaginal tissue (≥ 0.90) compared to cell populations collected from hands without prior contact with vaginal tissue. Additionally, digital penetration cell populations may be resolved from saliva cell populations and other non-target tissue types.

Indexed as

Forensic MedicineSex OffensesCell DifferentiationDNAEpidermal CellsFemaleHumansDNABiological mixturesDigital penetrationImaging flow cytometrySexual assaultTrace epidermal cellsVaginal

Identifiers

PMID37399646
PMCPMC10528675
OpenAlexW4382199798

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.