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

Utilizing Massively Parallel Sequencing (MPS) of Human Leukocyte Antigen (HLA) Gene Polymorphism to Assess Relatedness in Deficiency Parentage Testing.

Genes - 24 Jan 2024

Kouniaki Diamanto I, Fotopoulos Konstantinos V, Tarassi Katerina, Tsirogianni Alexandra

Abstract excerpt

In the realm of DNA testing with legal implications, the reliability and precision of genetic markers play a pivotal role in confirming or negating paternity claims. This study aimed to assess the potential utility of human leukocyte antigen (HLA) gene polymorphism through massively parallel sequencing (MPS) technology as robust forensic markers for parentage testing involving genetic deficiencies. It sought to...

Read the complete abstract on PubMed

Topics

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

Share to Alleles
Share to DNA Fingerprinting

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to High-Throughput Nucleotide Sequencing

Share to HLA Antigens

Share to Paternity

Share to Polymorphism, Genetic

Share to Reproducibility of Results

Source

Open in PubMed Open full text

Identifiers

PMID: 38397140
DOI: 10.3390/genes15020150
PMCID: PMC10888046

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Utilizing Massively Parallel Sequencing (MPS) of Human Leukocyte Antigen (HLA) Gene Polymorphism to Assess Relatedness in Deficiency Parentage Testing.PMID 38397140Read ↗

Forensic application of a novel MPS-based panel (90 STRs and 100 SNPs) in a non-exclusion parentage case with three autosomal STRs incompatibilities.Semantic proximity Read ↗

Application of massively parallel sequencing (MPS) in paternity testing - case report.Semantic proximity Read ↗

Haplotype counting by next-generation sequencing for ultrasensitive human DNA detection.Semantic proximity Read ↗

Paternity testing using massively parallel sequencing and the PowerSeq™ AUTO/Y system for short tandem repeat sequencing.Semantic proximity Read ↗

More comprehensive forensic genetic marker analyses for accurate human remains identification using massively parallel DNA sequencing.Semantic proximity Read ↗

Genetics and genomics of core short tandem repeat loci used in human identity testing.Semantic proximity Read ↗

Complex kinship analysis with a combination of STRs, SNPs, and indels.Semantic proximity Read ↗

Application of a short amplicon triallelic SNP panel for parentage analysis of highly degraded DNA.Semantic proximity Read ↗

Forensic investigative genetic genealogy: expanding pedigree tracing and genetic inquiry in the genomic era.Semantic proximity Read ↗

Applying massively parallel sequencing to paternity testing on the Ion Torrent Personal Genome Machine.Semantic proximity Read ↗

A novel 193-plex MPS panel integrating STRs and SNPs highlights the application value of forensic genetics in individual identification and paternity testing.Semantic proximity Read ↗

Implications of uniparental disomy in forensic kinship testing: A case study of paternal isodisomy on chromosome 3.Semantic proximity Read ↗

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