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

Forensic Implications of the Discrepancies Caused between NGS and CE Results by New Microvariant Allele at Penta E Microsatellite.

Genes - 18 May 2023

Kocsis Balázs, Mátrai Norbert, Egyed Balázs

Abstract excerpt

Examination of STR markers using the MPS technology is becoming more common in forensic genetics, but scientists still have insufficient experience in dealing with ambiguous results. However, it is always essential to resolve discordant data if we want to use the technology as an accredited method in routine forensic casework. During the internal laboratory validation of the Precision ID GlobalFiler NGS STR Panel...

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
Share to High-Throughput Nucleotide Sequencing

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Microsatellite Repeats

Source

Open in PubMed Open full text

Identifiers

PMID: 37239469
DOI: 10.3390/genes14051109
PMCID: PMC10218238

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Forensic Implications of the Discrepancies Caused between NGS and CE Results by New Microvariant Allele at Penta E Microsatellite.PMID 37239469Read ↗

Discordance of Penta D x.4 microvariant alleles results between three capillary electrophoresis and one massively parallel sequencing short tandem repeat kits.Semantic proximity Read ↗

Massively parallel sequencing of 17 commonly used forensic autosomal STRs and amelogenin with small amplicons.Semantic proximity Read ↗

Prevalence and characterisation of size and sequence-based microvariant alleles at nine autosomal STR markers in the Central Indian population.Semantic proximity Read ↗

Molecular Characterization and Genetic Significance of a Rare Type-I Triallelic Pattern Involving a 15.3 Microvariant at the D19S433 Locus.Semantic proximity Read ↗

D5S818 Typing Discrepancy Between PowerPlex(®) Fusion and Other STR Kits Including GlobalFiler(®) Caused by a One-base Deletion in 31 Nucleotides Upstream of the Repeat Region.Semantic proximity Read ↗

Analysis of homozygous allele mismatches in paternity tests with massively parallel sequencing.Semantic proximity Read ↗

The development of mini pentameric STR loci for rapid analysis of forensic DNA samples on a microfluidic system.Semantic proximity Read ↗

Internal validation of the Precision ID GlobalFiler NGS STR panel v2 kit with locus-specific analytical threshold, and with special regard to mixtures and low template DNA detection.Semantic proximity Read ↗

Concordance testing between Powerplex ESI 16 Fast System and VeriFiler Express.Semantic proximity Read ↗

A comprehensive characterization of MPS-STR stutter artefacts.Semantic proximity Read ↗

Recognizing the advantage of employing the PowerPlex(®) ESI and PowerPlex(®) ESX complementary kits for purposes of clarification in routine casework.Semantic proximity Read ↗

Validation of a 16-locus fluorescent multiplex system.Semantic proximity Read ↗

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