Evidence map›Paper›PMID 42364032›Full record

ArticleMolecular biology reports2026

Update of Mexican population databases for complex kinship interpretation with twelve and seven X-STRs.

Irán Cortés-Trujillo, Mayra Elizabeth García-Aceves, Eduardo Rojas-Prado, Mauro López-Armenta, Cinthya Miroslava Guzmán-González, Guadalupe Avalos-Navarro, Gabriela Martínez-Cortés, José Alonso Aguilar-Velázquez, Mariano Guardado-Estrada, Héctor Rangel-Villalobos

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Article in Molecular biology reports, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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2 · The registry

The trial behind it

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3 · Its place in the literature

Who cites it

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4 · The record

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5 · Who and what money

Authors and funding

10 authors.

Irán Cortés-Trujillo *Instituto de Investigación en Genética Molecular, Departamento de Ciencias Médicas y de la Vida, Centro Universitario de la Ciénega, Universidad de Guadalajara (CUCI-UdeG), Ocotlán, CP 47810, Jalisco, México.ORCID http://orcid.org/0009-0003-3286-9456
Mayra Elizabeth García-Aceves *Instituto de Investigación en Genética Molecular, Departamento de Ciencias Médicas y de la Vida, Centro Universitario de la Ciénega, Universidad de Guadalajara (CUCI-UdeG), Ocotlán, CP 47810, Jalisco, México.ORCID http://orcid.org/0000-0001-8546-9964
Eduardo Rojas-PradoDepartamento de Toxicología, Centro de Investigación y Estudios Avanzados (CINVESTAV) del Instituto Politécnico Nacional (IPN), Ciudad de México, México.ORCID http://orcid.org/0000-0003-1986-9964
Mauro López-ArmentaInstituto de Servicios Periciales y Ciencias Forenses (INCIFO), Poder Judicial de la Ciudad de México, Ciudad de México, México.
Cinthya Miroslava Guzmán-GonzálezLaboratorio de Genética, Escuela Nacional de Ciencias Forenses, Universidad Nacional Autónoma de México, Ciudad de México, México.
Guadalupe Avalos-NavarroInstituto de Investigación en Genética Molecular, Departamento de Ciencias Médicas y de la Vida, Centro Universitario de la Ciénega, Universidad de Guadalajara (CUCI-UdeG), Ocotlán, CP 47810, Jalisco, México.ORCID http://orcid.org/0000-0003-1121-607X
Gabriela Martínez-CortésInstituto de Investigación en Genética Molecular, Departamento de Ciencias Médicas y de la Vida, Centro Universitario de la Ciénega, Universidad de Guadalajara (CUCI-UdeG), Ocotlán, CP 47810, Jalisco, México.ORCID http://orcid.org/0000-0002-3947-4612
José Alonso Aguilar-VelázquezLaboratorio de Ciencias Morfológico Forenses y Medicina Molecular, Departamento de Morfología, Centro Universitario de Ciencias de la Salud, Universidad de Guadalajara, Guadalajara, Jalisco, México.ORCID http://orcid.org/0000-0002-5346-5595
Mariano Guardado-EstradaLaboratorio de Genética, Escuela Nacional de Ciencias Forenses, Universidad Nacional Autónoma de México, Ciudad de México, México. mguardado@enacif.unam.mx.ORCID http://orcid.org/0000-0001-8790-5504
Héctor Rangel-VillalobosInstituto de Investigación en Genética Molecular, Departamento de Ciencias Médicas y de la Vida, Centro Universitario de la Ciénega, Universidad de Guadalajara (CUCI-UdeG), Ocotlán, CP 47810, Jalisco, México. hrangel13@hotmail.com.ORCID http://orcid.org/0000-0003-2641-8782

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundX-chromosome short tandem repeats (X-STRs) are valuable for resolving complex kinship cases. Most population databases are based on the ArgusX12 kit (Qiagen), using PCR and capillary electrophoresis (CE) to identify length-based (LB) alleles, and are formatted for FamlinkX software. However, haplotype diversity is often underrepresented by population studies, compelling database updates ( https://famlink.se/fx_databases.html ). The ForenSeq DNA Signature Prep kit (Verogen) uses massive parallel sequencing (MPS) to analyze 7 X-STRs and report sequence-based (SB) alleles, for which population databases are currently unavailable. Because these 7 markers are a subset of the ArgusX12 panel, existing LB-based databases can support kinship interpretation of MPS-derived data. METHODS AND

resultsWe therefore updated a Mexican population database for 12 X-STRs and generated a corresponding 7-marker subset with FamlinkX-compatible files. Using 500 haplotypes from the Investigator Argus X-12 kit QS (Qiagen), we estimated forensic parameters and evaluated the impact of the updated database by calculating likelihood ratios (LRs) in four representative kinship scenarios. The updated database (n = 1433) increased LRs by an average of 55% compared to the previous version (n = 933).

conclusionsThese results support improved forensic interpretation in Mexican and Latin American populations lacking comprehensive national X-STR databases based on ArgusX12 and ForenSeq DNA Signature kits.

Indexed as

Chromosomes, Human, XMicrosatellite RepeatsAllelesDatabases, GeneticDNA FingerprintingElectrophoresis, CapillaryFemaleForensic GeneticsGene FrequencyGenetics, PopulationHaplotypesHigh-Throughput Nucleotide SequencingHumansMaleMexicoPedigreeArgus X-12FamlinkXKinshipMexicoX-STRs

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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.