Developmental validation of the ForenSeq MainstAY kit, MiSeq FGx sequencing system and ForenSeq Universal Analysis Software

被引:13
作者
Stephens, Kathryn M. [1 ]
Barta, Richelle [1 ]
Fleming, Keenan [1 ]
Perez, Juan Carlos [1 ]
Wu, Shan-Fu [1 ]
Snedecor, June [1 ]
Holt, Cydne L. [1 ]
LaRue, Bobby [1 ]
Budowle, Bruce [2 ]
机构
[1] Verogen Inc, 11111 Flintkote Ave, San Diego, CA 92121 USA
[2] Univ Helsinki, Dept Forens Med, Haartmaninkatu 8,POB 63, Helsinki 00014, Finland
关键词
ForenSeq MainstAY; MiSeq FGx System; ForenSeq universal analysis software; MiSeq FGx reagent micro kit; Massively parallel sequencing; Next generation sequencing; Short tandem repeat (STR); SWGDAM validation; SIGNATURE PREP KIT; PCR AMPLIFICATION KIT; STR LOCI; MITOCHONDRIAL GENOME; HIGH-QUALITY; DNA; MULTIPLEX; PERFORMANCE; IDENTIFICATION; DATABASE;
D O I
10.1016/j.fsigen.2023.102851
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
For human identification purposes, forensic genetics has primarily relied upon a core set of autosomal (and to a lesser extent Y chromosome) short tandem repeat (STR) markers that are enriched by amplification using the polymerase chain reaction (PCR) that are subsequently separated and detected using capillary electrophoresis (CE). While STR typing conducted in this manner is well-developed and robust, advances in molecular biology that have occurred over the last 15 years, in particular massively parallel sequencing (MPS) [1-7], offer certain advantages as compared to CE-based typing. First and foremost is the high throughput capacity of MPS. Current bench top high throughput sequencers enable larger batteries of markers to be multiplexed and multiple samples to be sequenced simultaneously (e.g., millions to billions of nucleotides can be sequenced in one run). Second, compared to the length-based CE approach, sequencing STRs increases discrimination power, enhances sensitivity of detection, reduces noise due to instrumentation, and improves mixture interpretation [4,8-23]. Third, since detection of STRs is based on sequence and not fluorescence, amplicons can be designed that are shorter in length and of similar lengths among loci, where possible, which can improve amplification efficiency and analysis of degraded samples. Lastly, MPS offers a single format approach that can be applied to analysis of a wide variety of genetic markers of forensic interest (e.g., STRs, mitochondrial DNA, single nucleotide polymorphisms, insertion/deletions). These features make MPS a desirable technology for casework [14,15,24, 25-48]. The developmental validation of the ForenSeq MainstAY library preparation kit with the MiSeq FGx Sequencing System and ForenSeq Universal Software is reported here to assist with validation of this MPS system for casework [49]. The results show that the system is sensitive, accurate and precise, specific, and performs well with mixtures and mock case-type samples.
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页数:20
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