Recovery of Whole Mitochondrial Genome From Compromised Samples Via Multiplex PCR and Massively Parallel Sequencing
Author(s) -
Maureen Peters Hickman,
Kelly Grisedale,
Brittania J. Bintz,
Erin S Burnside,
Erin Hanson,
Jack Ballantyne,
Mark R. Wilson
Publication year - 2018
Publication title -
future science oa
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.825
H-Index - 23
ISSN - 2056-5623
DOI - 10.4155/fsoa-2018-0059
Subject(s) - massive parallel sequencing , multiplex , mitochondrial dna , biology , dna sequencing , computational biology , genome , dna , multiplex polymerase chain reaction , whole genome sequencing , multiple displacement amplification , buccal swab , genetics , microbiology and biotechnology , polymerase chain reaction , gene , dna extraction
In forensic casework, compromised samples often possess limited or degraded nuclear DNA, rendering mitochondrial DNA a more feasible option for forensic DNA analyses. The emergence of massively parallel sequencing (MPS) has enabled the recovery of extensive sequence information from very low quantities of DNA. We have developed a multiplex PCR method that amplifies the complete mitochondrial genome in a range of forensically relevant samples including single cells, cremated remains, bone, maggot and hairs isolated from dust bunnies. Following library preparation, MPS yields complete or nearly complete mitochondrial genome coverage for all samples. To confirm concordance between sample types and between sequencing platforms, we compared sequencing results from hair and buccal swabs from two references. Low initial DNA input into the multiplex PCR allows for conservation of precious DNA while MPS maximizes recovery of genetic information.
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