Forensic massively parallel sequencing data analysis tool: Implementation of MyFLq as a standalone web- and Illumina BaseSpace®-application

被引:17
|
作者
Van Neste, Christophe [1 ]
Gansemans, Yannick [1 ]
De Coninck, Dieter [1 ]
Van Hoofstat, David [1 ]
Van Criekinge, Wim [2 ]
Deforce, Dieter [1 ]
Van Nieuwerburgh, Filip [1 ]
机构
[1] Univ Ghent, Fac Pharmaceut Sci, Lab Pharmaceut Biotechnol, B-9000 Ghent, Belgium
[2] Univ Ghent, Fac Biosci Engn, Biobix, B-9000 Ghent, Belgium
关键词
Illumina; MiSeq; STR; Forensic loci; MPS; NGS; GENOMES; QUALITY;
D O I
10.1016/j.fsigen.2014.10.006
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Routine use of massively parallel sequencing (MPS) for forensic genomics is on the horizon. The last few years, several algorithms and workflows have been developed to analyze forensic MPS data. However, none have yet been tailored to the needs of the forensic analyst who does not possess an extensive bioinformatics background. We developed our previously published forensic MPS data analysis framework MyFLq (My-Forensic-Loci-queries) into an open-source, user-friendly, web-based application. It can be installed as a standalone web application, or run directly from the Illumina BaseSpace environment. In the former, laboratories can keep their data on-site, while in the latter, data from forensic samples that are sequenced on an Illumina sequencer can be uploaded to Basespace during acquisition, and can subsequently be analyzed using the published MyFLq BaseSpace application. Additional features were implemented such as an interactive graphical report of the results, an interactive threshold selection bar, and an allele length-based analysis in addition to the sequenced-based analysis. Practical use of the application is demonstrated through the analysis of four 16-plex short tandem repeat (STR) samples, showing the complementarity between the sequence-and length-based analysis of the same MPS data. (C) 2014 The Authors. Published by Elsevier Ireland Ltd.
引用
收藏
页码:2 / 7
页数:6
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