Sukser, Viktorija; Rokić, Filip; Barbarić, Lucija; Korolija, Marina
(2021)
Assessment of Illumina® Human mtDNA Genome assay: workflow evaluation with development of analysis and interpretation guidelines.
International Journal of Legal Medicine
.
ISSN 0937-9827
(In Press)
Abstract
Mitochondrial DNA (mtDNA) is a small but significant part of the human genome,
whose applicability potential has gradually increased with the advent of massively
parallel sequencing (MPS) technology. Knowledge of the particular workflow,
equipment and reagents used, along with extensive usage of negative controls to
monitor all preparation steps constitute the prerequisites for confident reporting of
results. In this study, we performed assessment of Illumina® Human mtDNA Genome
assay on MiSeq FGx TM instrument. Through analysis of several types of negative
controls, as well as mtDNA positive controls, we established thresholds for data
analysis and interpretation, consisting of several components: minimum read depth
(220 reads), minimum quality score (41), percentage of minor allele sufficient for
analysis (3.0%), percentage of minor allele sufficient for interpretation (6.0%), and
percentage of major allele sufficient for homoplasmic variant call (97.0%). Based on
these criteria, we defined internal guidelines for analysis and interpretation of mtDNA
results obtained by MPS. Our study shows that the whole mtDNA assay on MiSeq FGx
TM produces repeatable and reproducible results, independent of analyst, which are
also concordant with Sanger-type sequencing results for mtDNA control region, as well
as with MPS results produced by NextSeq®. Overall, established thresholds and
interpretation guidelines were successfully applied for sequencing of complete
mitochondrial genomes from high-quality samples. The underlying principles and
proposed methodology on definition of internal laboratory guidelines for analysis and
interpretation of MPS results may be applicable to similar MPS workflows, primarily in
forensic genetics and molecular diagnostics.
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