Literature DB >> 30739830

Automation and developmental validation of the ForenSeq DNA Signature Preparation kit for high-throughput analysis in forensic laboratories.

Clémence Hollard1, Lionel Ausset2, Yann Chantrel1, Sandrine Jullien1, Maéva Clot1, Magalie Faivre1, Élodie Suzanne1, Laurent Pène1, François-Xavier Laurent3.   

Abstract

Massively parallel sequencing (MPS) applications in forensic science highlight the advantages of this technique compared to capillary electrophoresis (CE). The multiplexing of a wide range of genetic markers and access to the full amplicon sequence, allowing the detection of isoalleles, make it a very promising tool which could be applied to the most challenging casework DNA samples. However, the complexity of the manual library preparation protocol, potential DNA contamination and sample tracking issues are the main reasons why forensic scientists still hesitate to implement MPS analytical workflows in their laboratory. Here, we present the automation of all library preparation steps for up to 96 samples using the Verogen's ForenSeq™ DNA Signature Preparation kit. This automated protocol, developed on a Hamilton ID STARlet robotic platform, is designed to allow the combined sequencing of rich and poor DNA samples thanks to a final step which adjusts normalized library pooling volume to guarantee a uniform depth of coverage across all samples. Our study includes tests of concordance, repeatability, reproducibility and sensitivity (1000 pg, 700 pg, 500 pg, 250 pg, 100 pg and 50 pg). Sequencing results obtained with the automated protocol were found to be concordant with previous validation studies using the manual protocol in terms of depth of coverage and allele coverage ratio. The results of this study will assist forensic laboratories seeking to acquire a plug and play solution to optimize the processing and analysis of casework samples with MPS.
Copyright © 2019 Elsevier B.V. All rights reserved.

Entities:  

Keywords:  Automation; Forensic genomics; Library pooling; Library preparation; Multiple parallel sequencing; Validation

Mesh:

Year:  2019        PMID: 30739830     DOI: 10.1016/j.fsigen.2019.01.010

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


  5 in total

1.  Sequencing of human identification markers in an Uyghur population using the MiSeq FGxTM Forensic Genomics System.

Authors:  Halimureti Simayijiang; Niels Morling; Claus Børsting
Journal:  Forensic Sci Res       Date:  2020-09-10

2.  Exploring STR sequencing for forensic DNA intelligence databasing using the Austrian National DNA Database as an example.

Authors:  Petra Hölzl-Müller; Martin Bodner; Burkhard Berger; Walther Parson
Journal:  Int J Legal Med       Date:  2021-08-26       Impact factor: 2.686

Review 3.  An Introductory Overview of Open-Source and Commercial Software Options for the Analysis of Forensic Sequencing Data.

Authors:  Tunde I Huszar; Katherine B Gettings; Peter M Vallone
Journal:  Genes (Basel)       Date:  2021-10-29       Impact factor: 4.096

4.  Opportunity of Next-Generation Sequencing-Based Short Tandem Repeat System for Tumor Source Identification.

Authors:  Anqi Chen; Lei Xiong; Yiling Qu; Shihan Xi; Ruiyang Tao; Chengtao Li; Suhua Zhang
Journal:  Front Oncol       Date:  2022-02-11       Impact factor: 6.244

5.  Validation and beyond: Next generation sequencing of forensic casework samples including challenging tissue samples from altered human corpses using the MiSeq FGx system.

Authors:  Alina Senst; Amke Caliebe; Eva Scheurer; Iris Schulz
Journal:  J Forensic Sci       Date:  2022-03-22       Impact factor: 1.717

  5 in total

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