Literature DB >> 31812097

Comparison of CE- and MPS-based analyses of forensic markers in a single cell after whole genome amplification.

Man Chen1, Jingjing Zhang2, Jing Zhao3, Tong Chen1, Zhiyong Liu1, Feng Cheng4, Qingwei Fan4, Jiangwei Yan5.   

Abstract

Whole genome amplification (WGA) allows for multiple genetic analyses with low template DNA, such as DNA derived from a single cell. WGA could increase the amount of input DNA from the pg to the μg level. However, there are no studies comparing the performance of forensic markers with DNA from a single cell after WGA evaluated on both capillary electrophoresis (CE) and massively parallel sequencing (MPS) platforms. In this study, cell lines consisting of female cultured B-lymphoblastoid cells and karyocytes from male venous blood were segregated into one, two, three and five cells. Including the references with the bulk cells, all samples were generated by WGA with the multiple displacement amplification (MDA) strategy in triplicate and genotyped on CE and MPS platforms. Allele balance, stutter ratio, accuracy, repeatability and concordance of short tandem repeat (STR) markers were used to evaluate the genotyping performance on both platforms. Additionally, the sequence coverage ratio (SCR) and SNP genotypes were evaluated for sequence information generated from the MPS. Heterozygous loci showed high allele balance, with an overall average allele balance ratio larger than 0.79 on the CE and 0.75 on the MPS platforms for the venous blood cell samples; the cultured B-lymphoblastoid cell samples had ratios of 0.62 and 0.70, respectively. The stutter ratio of every source and cell number from both cell line samples were very close, ranging from 5.3%-7.2% for autosomal STRs and approximately 10 % of Y chromosomal STRs on the CE platform. The average stutter, allele, and sequence-based and length-based noise ratios were 6.6 %, 88 %, 4.7 % and 0.7 %, respectively, in the single male cell sample. SNPs also showed high consistency and intralocus balance. Our study indicated that WGA with MDA strategy works relatively well of STR and SNP genotyping with low copy number samples on CE and MPS, even with one-cell sample.
Copyright © 2019 Elsevier B.V. All rights reserved.

Keywords:  Capillary electrophoresis; Forensic loci; Low copy number; Massively parallel sequencing; Whole genome amplification

Mesh:

Substances:

Year:  2019        PMID: 31812097     DOI: 10.1016/j.fsigen.2019.102211

Source DB:  PubMed          Journal:  Forensic Sci Int Genet        ISSN: 1872-4973            Impact factor:   4.882


  4 in total

1.  Kinship analysis on single cells after whole genome amplification.

Authors:  Jana Weymaere; Ann-Sophie Vander Plaetsen; Laurentijn Tilleman; Olivier Tytgat; Kaat Rubben; Sofie Geeraert; Dieter Deforce; Filip Van Nieuwerburgh
Journal:  Sci Rep       Date:  2020-09-04       Impact factor: 4.379

2.  Precision DNA Mixture Interpretation with Single-Cell Profiling.

Authors:  Jianye Ge; Jonathan L King; Amy Smuts; Bruce Budowle
Journal:  Genes (Basel)       Date:  2021-10-20       Impact factor: 4.096

Review 3.  Recent advances and application of whole genome amplification in molecular diagnosis and medicine.

Authors:  Xiaoyu Wang; Yapeng Liu; Hongna Liu; Wenjing Pan; Jie Ren; Xiangming Zheng; Yimin Tan; Zhu Chen; Yan Deng; Nongyue He; Hui Chen; Song Li
Journal:  MedComm (2020)       Date:  2022-02-03

Review 4.  New Perspectives for Whole Genome Amplification in Forensic STR Analysis.

Authors:  Richard Jäger
Journal:  Int J Mol Sci       Date:  2022-06-25       Impact factor: 6.208

  4 in total

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