Evidence map›Paper›PMID 28078444›Full record

ArticleInternational journal of legal medicine2017

MPS analysis of the mtDNA hypervariable regions on the MiSeq with improved enrichment.

Mitchell M Holland, Laura A Wilson, Sarah Copeland, Gloria Dimick, Charity A Holland, Robert Bever, Jennifer A McElhoe

Abstract read
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Article in International journal of legal medicine, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.9field-weighted citation impact, top 27% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

3 citing papers in PubMed, 17 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors at 4 institutions in 1 country.

Mitchell M HollandForensic Science Program, Department of Biochemistry & Molecular Biology, The Pennsylvania State University, 339 Whitmore Laboratory, University Park, PA, 16802, USA. mmh20@psu.edu.
Laura A WilsonBode Cellmark Forensics (a LabCorp Specialty Testing Group), 10430 Furnace Road, Suite 107, Lorton, VA, 22079, USA.
Sarah CopelandMitotyping Technologies (a division of Health Network Laboratories), 2565 Park Center Blvd, Suite 200, State College, PA, 16801, USA.
Gloria DimickMitotyping Technologies (a division of Health Network Laboratories), 2565 Park Center Blvd, Suite 200, State College, PA, 16801, USA.
Charity A HollandForensic Science Program, Department of Biochemistry & Molecular Biology, The Pennsylvania State University, 339 Whitmore Laboratory, University Park, PA, 16802, USA.
Robert BeverBode Cellmark Forensics (a LabCorp Specialty Testing Group), 10430 Furnace Road, Suite 107, Lorton, VA, 22079, USA.
Jennifer A McElhoeForensic Science Program, Department of Biochemistry & Molecular Biology, The Pennsylvania State University, 339 Whitmore Laboratory, University Park, PA, 16802, USA.
Pennsylvania State University · USLabCorp (United States) · USHealth Net · USNetwork Technologies (United States) · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The non-coding displacement (D) loop of the human mitochondrial (mt) genome contains two hypervariable regions known as HVR1 and HVR2 that are most often analyzed by forensic DNA laboratories. The massively parallel sequencing (MPS) protocol from Illumina (Human mtDNA D-Loop Hypervariable Region protocol) utilizes four sets of established PCR primer pairs for the initial amplification (enrichment) step that span the hypervariable regions. Transposase adapted (TA) sequences are attached to the 5'-end of each primer, allowing for effective library preparation prior to analysis on the MiSeq, and AmpliTaq Gold DNA polymerase is the enzyme recommended for amplification. The amplification conditions were modified by replacing AmpliTaq Gold with TaKaRa Ex Taq® HS, along with an enhanced PCR buffer system. The resulting method was compared to the recommended protocol and to a conventional non-MPS approach used in an operating forensic DNA laboratory. The modified amplification conditions gave equivalent or improved results, including when amplifying low amounts of DNA template from hair shafts which are a routine evidence type in forensic mtDNA cases. Amplification products were successfully sequenced using an MPS approach, addressing sensitivity of library preparation, evaluation of precision and accuracy through repeatability and reproducibility, and mixture studies. These findings provide forensic laboratories with a robust and improved enrichment method as they begin to implement the D-loop protocol from Illumina. Given that Ex Taq® HS is a proofreading enzyme, using this approach should allow for improved analysis of low-level mtDNA heteroplasmy.

Indexed as

High-Throughput Nucleotide SequencingDNA-Directed DNA PolymeraseDNA, MitochondrialGenome, MitochondrialHairHumansPolymerase Chain ReactionReproducibility of ResultsDNA-Directed DNA PolymeraseDNA, MitochondrialD-loopForensic scienceHeteroplasmyMassively parallel sequencingMitochondrial DNAMPSPCR

Identifiers

PMID28078444
OpenAlexW2578095890

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.