基因分型
SNP公司
单核苷酸多态性
SNP基因分型
遗传学
分子反转探针
打字
生物
计算生物学
DNA测序
DNA
SNP阵列
基因型
基因
作者
Anqi Chen,Lun Li,Junfei Zhou,Tiantian Li,Chunyan Yuan,Hai Peng,Chengtao Li,Suhua Zhang
标识
DOI:10.3389/fgene.2024.1432378
摘要
Introduction Multiple linked single nucleotide polymorphisms (SNPs) have shown potential in personal identification and mixture detection. However, the limited number of marker and sequencing errors have obstructed accurate DNA typing. Methods To develop more candidate loci, the diversity value (D-value) was introduced as a new parameter for screening the novel polymorphic multiple linked-SNP markers, referred to as multi-SNP. In this study, a “FD Multi-SNP Mixture Kit” comprising 567 multi-SNPs was developed for mixture detection. Additionally, a new computational error correction method was applied as a quality control approach for sequencing data. Results The results demonstrated higher typing success rates than the conventional CE typing method. For single-source DNA, approximately 70–80 loci were detected with a DNA input of 0.009765625 ng. More than 65% of the minor alleles were distinguishable at 1 ng DNA with a frequency of 0.5% in 2- to 4-person mixtures. Conclusion This study offers a polymorphic and high-resolution detection method for DNA genotyping and complex mixture detection, providing an alternative strategy for addressing challenging mixed DNA traces.
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