Recovery of single source DNA profiles from mixtures by direct single cell subsampling and simplified micromanipulation

2021 ◽  
Vol 61 (1) ◽  
pp. 13-25
Author(s):  
Kaitlin Huffman ◽  
Erin Hanson ◽  
Jack Ballantyne
2021 ◽  
Author(s):  
Kaitlin Huffman ◽  
Erin Hanson ◽  
Jack Ballantyne

DNA mixtures are a common source of crime scene evidence and are often one of the more difficult sources of biological evidence to interpret. With the implementation of probabilistic genotyping (PG), mixture analysis has been revolutionized allowing previously unresolvable mixed profiles to be analyzed and probative genotype information from contributors to be recovered. However, due to allele overlap, artifacts, or low-level minor contributors, genotype information loss inevitably occurs. In order to reduce the potential loss of significant DNA information from donors in complex mixtures, an alternative approach is to physically separate individual cells from mixtures prior to performing DNA typing thus obtaining single source profiles from contributors. In the present work, a simplified micro-manipulation technique combined with enhanced single-cell DNA typing was used to collect one or few cells, referred to as direct single-cell subsampling (DSCS). Using this approach, single and 2-cell subsamples were collected from 2-6 person mixtures. Single-cell subsamples resulted in single source DNA profiles while the 2-cell subsamples returned either single source DNA profiles or new mini-mixtures that are less complex than the original mixture due to the presence of fewer contributors. PG (STRmixTM) was implemented, after appropriate validation, to analyze the original bulk mixtures, single source cell subsamples, and the 2-cell mini mixture subsamples from the original 2-6-person mixtures. PG further allowed replicate analysis to be employed which, in many instances, resulted in a significant gain of genotype information such that the returned donor likelihood ratios (LRs) were comparable to that seen in their single source reference profiles (i.e., the reciprocal of their random match probabilities). In every mixture, the DSCS approach gave improved results for each donor compared to standard bulk mixture analysis. With the 5- and 6- person complex mixtures, DSCS recovered highly probative LRs (> 1020) from donors that had returned non-probative LRs (<103) by standard methods.


2017 ◽  
Vol 29 ◽  
pp. 126-144 ◽  
Author(s):  
Tamyra R. Moretti ◽  
Rebecca S. Just ◽  
Susannah C. Kehl ◽  
Leah E. Willis ◽  
John S. Buckleton ◽  
...  

2004 ◽  
Vol 49 (3) ◽  
pp. 1-8 ◽  
Author(s):  
John H. Ryan ◽  
Jeffrey K. Barrus ◽  
Bruce Budowle ◽  
Cynthia M. Shannon ◽  
Victor W. Thompson ◽  
...  

2020 ◽  
Vol 44 ◽  
pp. 102192 ◽  
Author(s):  
Sarah Riman ◽  
Hari Iyer ◽  
Lisa A. Borsuk ◽  
Peter M. Vallone
Keyword(s):  

2013 ◽  
Vol 7 (5) ◽  
pp. 516-528 ◽  
Author(s):  
Duncan Taylor ◽  
Jo-Anne Bright ◽  
John Buckleton
Keyword(s):  

2020 ◽  
Vol 21 (8) ◽  
pp. 602-609
Author(s):  
Caixia Gao ◽  
Mingnan Zhang ◽  
Lei Chen

The cell is the unit of life for all organisms, and all cells are certainly not the same. So the technology to generate transcription expression or genomic DNA profiles from single cells is crucial. Since its establishment in 2009, single-cell RNA sequencing (scRNA-seq) has emerged as a major driver of progress in biomedical research. During the last three years, several new single-cell sequencing platforms have emerged. Yet there are only a few systematic comparisons of the advantages and limitations of these commonly used platforms. Here we compare two single-cell sequencing platforms: BD Rhapsody and 10x Genomics Chromium, including their different mechanisms and some scRNA-seq results obtained with them.


Author(s):  
Debby A. Jennings ◽  
Michael J. Morykwas ◽  
Louis C. Argenta

Grafts of cultured allogenic or autogenic keratlnocytes have proven to be an effective treatment of chronic wounds and burns. This study utilized a collagen substrate for keratinocyte and fibroblast attachment. The substrate provided mechanical stability and augmented graft manipulation onto the wound bed. Graft integrity was confirmed by light and transmission electron microscopy.Bovine Type I dermal collagen sheets (100 μm thick) were crosslinked with 254 nm UV light (13.5 Joules/cm2) to improve mechanical properties and reduce degradation. A single cell suspension of third passage neonatal foreskin fibroblasts were plated onto the collagen. Five days later, a single cell suspension of first passage neonatal foreskin keratinocytes were plated on the opposite side of the collagen. The grafts were cultured for one month.The grafts were fixed in phosphate buffered 4% formaldehyde/1% glutaraldehyde for 24 hours. Graft pieces were then washed in 0.13 M phosphate buffer, post-fixed in 1% osmium tetroxide, dehydrated, and embedded in Polybed 812.


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