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

Developmental validation of the STRSeqTyper122 kit for massively parallel sequencing of forensic STRs.

International journal of legal medicine - 1 Jul 2024

Guo Li-Liang, Yuan Jia-Hui, Zhang Chi, Zhao Jie, Yao Yi-Ren, Guo Ke-Li, Meng Yang, Ji An-Quan, Kang Ke-Lai, Wang Le

Abstract excerpt

Massively parallel sequencing allows for integrated genotyping of different types of forensic markers, which reduces DNA consumption, simplifies experimental processes, and provides additional sequence-based genetic information. The STRseqTyper122 kit genotypes 63 autosomal STRs, 16 X-STRs, 42 Y-STRs, and the Amelogenin locus. Amplicon sizes of 117 loci were below 300 bp. In this study, MiSeq FGx sequencing...

Read the complete abstract on PubMed

Topics

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

Share to Amelogenin
Share to DNA Degradation, Necrotic

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to DNA Fingerprinting

Share to Electrophoresis, Capillary

Share to High-Throughput Nucleotide Sequencing

Share to Microsatellite Repeats

Share to Reproducibility of Results

Share to Species Specificity

Source

Identifiers

PMID: 38416217
DOI: 10.1007/s00414-024-03195-2

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

Developmental validation of the STRSeqTyper122 kit for massively parallel sequencing of forensic STRs.PMID 38416217Read ↗

Massively parallel sequencing of forensic STRs and SNPs using the Illumina® ForenSeq™ DNA Signature Prep Kit on the MiSeq FGx™ Forensic Genomics System.Semantic proximity Read ↗

Systematic evaluation of the Precision ID GlobalFiler™ NGS STR panel v2 using single-source samples of various quantity and quality and mixed DNA samples.Semantic proximity Read ↗

Sequence investigation of 34 forensic autosomal STRs with massively parallel sequencing.Semantic proximity Read ↗

Developmental validation of the MiSeq FGx Forensic Genomics System for Targeted Next Generation Sequencing in Forensic DNA Casework and Database Laboratories.Semantic proximity Read ↗

Systematic assessment of the performance of illumina's MiSeq FGx™ forensic genomics system.Semantic proximity Read ↗

A preliminary assessment of the ForenSeq™ FGx System: next generation sequencing of an STR and SNP multiplex.Semantic proximity Read ↗

Applications and Performance of Precision ID GlobalFiler NGS STR, Identity, and Ancestry Panels in Forensic Genetics.Semantic proximity Read ↗

Current state-of-art of STR sequencing in forensic genetics.Semantic proximity Read ↗

Characterization of genetic sequence variation of 58 STR loci in four major population groups.Semantic proximity Read ↗

Accurate profiling of forensic autosomal STRs using the Oxford Nanopore Technologies MinION deviceSemantic proximity Read ↗

Inter-laboratory study on standardized MPS libraries: evaluation of performance, concordance, and sensitivity using mixtures and degraded DNA.Semantic proximity Read ↗

Developmental validation of the monSTR identity panel, a forensic STR multiplex assay for massively parallel sequencing.Semantic proximity Read ↗

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