Precision DNA Mixture Interpretation with Single-Cell Profiling

被引:9
作者
Ge, Jianye [1 ,2 ]
King, Jonathan L. [1 ]
Smuts, Amy [1 ]
Budowle, Bruce [1 ,2 ]
机构
[1] Univ North Texas, Hlth Sci Ctr, Ctr Human Identificat, Ft Worth, TX 76107 USA
[2] Univ North Texas, Hlth Sci Ctr, Dept Microbiol Immunol & Genet, Ft Worth, TX 76107 USA
关键词
DNA forensics; DNA mixture; mixture interpretation; single-cell; clustering algorithm; number of contributors; consensus profile; DEVELOPMENTAL VALIDATION; STR LOCI; SPERM; AMPLIFICATION; SEPARATION; IDENTIFICATION; VISUALIZATION; PROBABILITY; SOFTWARE; KIT;
D O I
10.3390/genes12111649
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Wet-lab based studies have exploited emerging single-cell technologies to address the challenges of interpreting forensic mixture evidence. However, little effort has been dedicated to developing a systematic approach to interpreting the single-cell profiles derived from the mixtures. This study is the first attempt to develop a comprehensive interpretation workflow in which single-cell profiles from mixtures are interpreted individually and holistically. In this approach, the genotypes from each cell are assessed, the number of contributors (NOC) of the single-cell profiles is estimated, followed by developing a consensus profile of each contributor, and finally the consensus profile(s) can be used for a DNA database search or comparing with known profiles to determine their potential sources. The potential of this single-cell interpretation workflow was assessed by simulation with various mixture scenarios and empirical allele drop-out and drop-in rates, the accuracies of estimating the NOC, the accuracies of recovering the true alleles by consensus, and the capabilities of deconvolving mixtures with related contributors. The results support that the single-cell based mixture interpretation can provide a precision that cannot beachieved with current standard CE-STR analyses. A new paradigm for mixture interpretation is available to enhance the interpretation of forensic genetic casework.
引用
收藏
页数:27
相关论文
共 70 条
[1]  
AABB, 2008, REL TEST ANN REP
[2]   viSNE enables visualization of high dimensional single-cell data and reveals phenotypic heterogeneity of leukemia [J].
Amir, El-ad David ;
Davis, Kara L. ;
Tadmor, Michelle D. ;
Simonds, Erin F. ;
Levine, Jacob H. ;
Bendall, Sean C. ;
Shenfeld, Daniel K. ;
Krishnaswamy, Smita ;
Nolan, Garry P. ;
Pe'er, Dana .
NATURE BIOTECHNOLOGY, 2013, 31 (06) :545-+
[3]  
Anslinger K, 2019, RECHTSMEDIZIN, V29, P30, DOI 10.1007/s00194-018-0291-1
[4]   Interpreting low template DNA profiles [J].
Balding, David J. ;
Buckleton, John .
FORENSIC SCIENCE INTERNATIONAL-GENETICS, 2009, 4 (01) :1-10
[5]   DNA PROFILE MATCH PROBABILITY CALCULATION - HOW TO ALLOW FOR POPULATION STRATIFICATION, RELATEDNESS, DATABASE SELECTION AND SINGLE BANDS [J].
BALDING, DJ ;
NICHOLS, RA .
FORENSIC SCIENCE INTERNATIONAL, 1994, 64 (2-3) :125-140
[6]   Developmental validation of STRmix™, expert software for the interpretation of forensic DNA profiles [J].
Bright, Jo-Anne ;
Taylor, Duncan ;
McGovern, Catherine ;
Cooper, Stuart ;
Russell, Laura ;
Abarno, Damien ;
Buckleton, John .
FORENSIC SCIENCE INTERNATIONAL-GENETICS, 2016, 23 :226-239
[7]   Single Cells for Forensic DNA Analysis-From Evidence Material to Test Tube [J].
Brueck, Simon ;
Evers, Heidrun ;
Heidorn, Frank ;
Mueller, Ute ;
Kilper, Roland ;
Verhoff, Marcel A. .
JOURNAL OF FORENSIC SCIENCES, 2011, 56 (01) :176-180
[8]   Validity of Low Copy Number Typing and Applications to Forensic Science [J].
Budowle, Bruce ;
Eisenberg, Arthur J. ;
van Daal, Angela .
CROATIAN MEDICAL JOURNAL, 2009, 50 (03) :207-217
[9]   Gene methylation and early detection of genitourinary cancer: the road ahead [J].
Cairns, Paul .
NATURE REVIEWS CANCER, 2007, 7 (07) :531-543
[10]   Single-cell whole-genome analyses by Linear Amplification via Transposon Insertion (LIANTI) [J].
Chen, Chongyi ;
Xing, Dong ;
Tan, Longzhi ;
Li, Heng ;
Zhou, Guangyu ;
Huang, Lei ;
Xie, X. Sunney .
SCIENCE, 2017, 356 (6334) :189-194