Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Analysis of data and common mutations encountered during routine parentage testing in Zimbabwe.

Scientific reports - 16 Jan 2024

Thelingwani Roslyn Stella, Jonhera Catherine Ashley, Masimirembwa Collen

Abstract excerpt

We analyzed parentage data collected over a ten-year period in a Zimbabwean DNA testing laboratory. Parentage case types, prevalence, exclusion data, mutations rates and observed genotyping irregularities were analyzed. We report analysis results from 1303 cases. DNA extraction and STR typing was conducted using standard commercial kits. Paternity was the most requested test (87.37%) followed by the indirect...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to DNA
Share to Microsatellite Repeats
Share to Mutation

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Paternity

Share to Pregnancy

Share to Zimbabwe

Source

Open in PubMed Open full text

Identifiers

PMID: 38228706
DOI: 10.1038/s41598-024-51987-8
PMCID: PMC10791675

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Analysis of data and common mutations encountered during routine parentage testing in Zimbabwe.PMID 38228706Read ↗

Paternity tests in Mexico: Results obtained in 3005 cases.Semantic proximity Read ↗

Assessing false paternity risk in simulated motherless cases from more than 20 000 real exclusion trios.Semantic proximity Read ↗

Observations and investigation of STR genotype inconsistencies due to mutations, silent alleles, and uniparental disomy in South African populations.Semantic proximity Read ↗

Analysis of short tandem repeat mutations in paternity cases from Masovian Voivodeship provinces form years 2018-2022 based on materials of the Department of Forensic Medicine, Medical University of Warsaw.Semantic proximity Read ↗

Detection of Mutations in Short Tandem Repeats (STRs) Loci in Paternity Testing in Romanian Population.Semantic proximity Read ↗

Mutation rates at 14 STR loci in the population from Pernambuco, Northeast Brazil.Semantic proximity Read ↗

Mutations of microsatellite autosomal loci in paternity investigations of the Southern Poland population.Semantic proximity Read ↗

[Mutations of short tandem repeat loci in Identifiler system].Semantic proximity Read ↗

New data on Short Tandem Repeat loci in Gabonese population: Tri-Allelic Patterns of Penta D and TPOX IdentifiedSemantic proximity Read ↗

Integrated Genetic Profiling for Cattle Parentage Testing via Next-Generation Sequencing.Semantic proximity Read ↗

Risk analysis of duo parentage testing with limited STR loci.Semantic proximity Read ↗

Allelic frequencies of 22 short tandem repeats loci and tri-allelic patterns of Penta D and TPOX identified in Gabonese population.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.