Human single nucleotide polymorphisms

摘要

Disclosed are methods for human identification utilizing newly discovered single nucleotide polymorphisms (SNPs) within CODIS loci which can cause allelic dropout. Also disclosed are kits useful in human identification.

主权项

1. A kit for human identification comprising: at least one pair of oligonucleotide primers for amplification of at least one locus selected from SEQ ID NO: 1 (D13S317), SEQ ID NO: 2 (TH01), SEQ ID NO: 3 (vWA), SEQ ID NO: 4(D12S391), and SEQ ID NO: 5 (D6S1043) wherein one primer of the pair hybridizes to a SNP nucleobase within a primer binding site of the at least one locus and at least one primer of the pair comprises a fluorescent label.