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

Improving DNA mixtures analysis using compound markers composed of InDels and SNPs screened from the whole genome with next-generation sequencing.

Electrophoresis - 1 Mar 2024

Tan Mengyu, Xue Jiaming, Wu Qiushuo, Zheng Yazi, Liu Guihong, Zhang Ranran, Wu Mengna, Song Jinlong, Xiao Yuanyuan, Chen Dezhi, Lv Meili, Liao Miao, Qu Shengqiu, Liang Weibo

Abstract excerpt

Next-generation sequencing (NGS) allows for better identification of insertion and deletion polymorphisms (InDels) and their combination with adjacent single nucleotide polymorphisms (SNPs) to form compound markers. These markers can improve the polymorphism of microhaplotypes (MHs) within the same length range, and thus, boost the efficiency of DNA mixture analysis. In this study, we screened InDels and SNPs...

Read the complete abstract on PubMed

Topics

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

Share to DNA
Share to DNA Fingerprinting

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Share to Gene Frequency

Share to High-Throughput Nucleotide Sequencing

Share to Polymorphism, Single Nucleotide

Share to Sequence Analysis, DNA

Source

Identifiers

PMID: 37946554
DOI: 10.1002/elps.202300195

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence. Graph snapshot: 2026-09-29.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Improving DNA mixtures analysis using compound markers composed of InDels and SNPs screened from the whole genome with next-generation sequencing.PMID 37946554Read ↗

Development and Evaluation of a Novel Microhaplotype Panel for DNA Mixture and Kinship Analysis.Semantic proximity Read ↗

Identification and sequencing of 59 highly polymorphic microhaplotypes for analysis of DNA mixtures.Semantic proximity Read ↗

A highly polymorphic panel of 40-plex microhaplotypes for the Chinese Han population and its application in estimating the number of contributors in DNA mixtures.Semantic proximity Read ↗

Evaluation of the Microhaplotypes panel for DNA mixture analyses.Semantic proximity Read ↗

A 124-plex Microhaplotype Panel Based on Next-generation Sequencing Developed for Forensic Applications.Semantic proximity Read ↗

Nanopore sequencing of MiniHap biomarkers for forensic DNA mixture deconvolution: A proof-of-principle study.Semantic proximity Read ↗

A Highly Polymorphic Panel Consisting of Microhaplotypes and Compound Markers with the NGS and Its Forensic Efficiency Evaluations in Chinese Two Groups.Semantic proximity Read ↗

Developmental and validation of a novel small and high-efficient panel of microhaplotypes for forensic genetics by the next generation sequencing.Semantic proximity Read ↗

Development a multiplex panel of AISNPs, multi-allelic InDels, microhaplotypes, and Y-SNP/InDel loci for multiple forensic purposes via the NGS.Semantic proximity Read ↗

Forensic applications of compound genetic markers: trends and future directions.Semantic proximity Read ↗

Developing and population analysis of a new multiplex panel of 18 microhaplotypes and compound markers using next generation sequencing and its application in the Shaanxi Han population.Semantic proximity Read ↗

Forensic applicability of multi-allelic InDels with mononucleotide homopolymer structures.Semantic proximity Read ↗

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