Evidence map›Paper›PMID 26614310›Full record

ArticleInternational journal of legal medicine2016

Mixtures with relatives and linked markers.

Guro Dørum, Daniel Kling, Andreas Tillmar, Magnus Dehli Vigeland, Thore Egeland

Abstract read
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Article in International journal of legal medicine, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
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

2 citing papers in PubMed.

  1. Article
  2. The forensic value of X-linked markers in mixed-male DNA analysis.International journal of legal medicine · 2018
    Article
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

5 authors.

Guro DørumDepartment of Chemistry, Biotechnology and Food Science, Norwegian University of Life Sciences, Aas, Norway. guro.dorum@nmbu.no.
Daniel KlingDepartment of Chemistry, Biotechnology and Food Science, Norwegian University of Life Sciences, Aas, Norway.
Andreas TillmarDepartment of Forensic Genetics and Forensic Toxicology, National Board of Forensic Medicine, Linköping, Sweden.
Magnus Dehli VigelandDepartment of Medical Genetics, University of Oslo and Oslo University Hospital, Oslo, Norway.
Thore EgelandDepartment of Chemistry, Biotechnology and Food Science, Norwegian University of Life Sciences, Aas, Norway.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Mixture DNA profiles commonly appear in forensic genetics, and a large number of statistical methods and software are available for such cases. However, most of the literature concerns mixtures where the contributors are assumed unrelated and the genetic markers are unlinked. In this paper, we consider mixtures of linked markers and related contributors. If no relationships are involved, linkage can be ignored. While unlinked markers can be treated independently, linkage introduces dependencies. The use of linked markers presents statistical and computational challenges, but may also lead to a considerable increase in power since the number of markers available is much larger if we do not require the markers to be unlinked. In addition, some cases that cannot be solved with an unlimited number of unlinked autosomal markers can be solved with linked markers. We focus on two special cases of linked markers: pairs of linked autosomal markers and X-chromosomal markers. A framework is presented for calculation of likelihood ratios for mixtures with general relationships and with linkage between any number of markers. Finally, we explore the effect of linkage disequilibrium, also called allelic association, on the likelihood ratio.

Indexed as

DNA FingerprintingGenetic LinkageGenetic MarkersChromosomes, Human, XFemaleForensic GeneticsHumansLikelihood FunctionsLinkage DisequilibriumMalePedigreeGenetic MarkersDNA mixturesForensicsKinshipLikelihood ratioLinkageLinkage disequilibrium

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Registered trials

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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.