Evidence map›Paper›PMID 32305739›Full record

ArticleForensic science international. Genetics2020

Validation of novel forensic DNA markers using multiplex microhaplotype sequencing.

Neeru Gandotra, William C Speed, Wenyi Qin, Yishuo Tang, Andrew J Pakstis, Kenneth K Kidd, Curt Scharfe

Open access · hybridAbstract readValidation Study
In one paragraph

Article in Forensic science international. Genetics, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
4.9field-weighted citation impact, top 5% 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

17 citing papers in PubMed, 41 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 1 institution in 1 country.

Neeru GandotraDepartment of Genetics, Yale University School of Medicine, New Haven, CT, 06520, USA.
William C SpeedDepartment of Genetics, Yale University School of Medicine, New Haven, CT, 06520, USA.
Wenyi QinDepartment of Genetics, Yale University School of Medicine, New Haven, CT, 06520, USA.
Yishuo TangDepartment of Genetics, Yale University School of Medicine, New Haven, CT, 06520, USA.
Andrew J PakstisDepartment of Genetics, Yale University School of Medicine, New Haven, CT, 06520, USA.
Kenneth K KiddDepartment of Genetics, Yale University School of Medicine, New Haven, CT, 06520, USA. Electronic address: kenneth.kidd@yale.edu.
Curt ScharfeDepartment of Genetics, Yale University School of Medicine, New Haven, CT, 06520, USA. Electronic address: curt.scharfe@yale.edu.
Yale University · US

Funding

Multiplex gene sequencing and metabolomics analysis from newborn dried blood spots to improve screening and diagnosis of metabolic disorders.R01HD102537 · NICHD · YALE UNIVERSITY · PI SCHARFE, CURT · 2020 to 2024
$3.0M
NICHD NIH HHS R01 HD102537
6 · The paper itself

Abstract

Microhaplotypes (MH) are comprised of multiple single nucleotide polymorphisms (SNPs) that are located within 300 bases of genomic sequence. Improved tools are needed to facilitate broader application of microhaplotypes in a diverse range of populations and forensic settings. We designed an assay for multiplex sequencing of 90 microhaplotypes (mMHseq) that include 46 MH loci with high Effective Number of Alleles (A

Indexed as

Genetic MarkersHaplotypesHigh-Throughput Nucleotide SequencingEthnicityForensic GeneticsGenetics, PopulationHumansSoftwareGenetic MarkersDiverse populationsForensicsMassively parallel sequencingMicrohaplotypeMPSSNPs

Identifiers

PMID32305739
PMCPMC10131188
OpenAlexW3011736213

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.