Evidence map›Paper›PMID 40149934›Full record

ArticleBiomolecules2025

Assessing Adventitious Matches of Non-Donors Related to True Contributors.

Kaitlin Huffman, Lilliana Moreno

Abstract read
In one paragraph

Article in Biomolecules, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

2 authors.

Kaitlin HuffmanDNA Support Unit, Federal Bureau of Investigation Laboratory, Quantico, VA 22135, USA.ORCID 0000-0001-9450-7854
Lilliana MorenoDNA Support Unit, Federal Bureau of Investigation Laboratory, Quantico, VA 22135, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Relatives share more DNA with one another than unrelated individuals. Therefore, there is an increased risk of close relatives (e.g., siblings or parents and children of true donors) adventitiously 'matching' DNA mixtures to which they are not a true contributor. One such method of addressing relatives is to utilize alternative propositions within probabilistic genotyping software (e.g., STRmix

Indexed as

DNAAllelesGenotypeHumansSiblingsSoftwareDNAcomplex mixturesprobabilistic genotypingrelated non-donors

Identifiers

PMID40149934
PMCPMC11940124

What OpenQuestion holds

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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.