Single nucleotide polymorphism (SNP)
Genome scans of facial features in East Africans and cross-population comparisons reveal novel associations
Reverse Complement-PCR, An Innovative and Effective Method for Multiplexing Forensically Relevant Single Nucleotide Polymorphism Marker Systems
Optimal processing for proteomic genotyping of single human hairs
Validation of novel forensic DNA markers using multiplex microhaplotype sequencing
Proteomic genotyping: Using mass spectrometry to infer SNP genotypes in pigmented and non-pigmented hair
STAT3 polymorphisms in North Africa and its implication in breast cancer
Utility of the Ion S5 (TM) and MiSeq FGx (TM) sequencing platforms to characterize challenging human remains
Development of NGS (next generation sequencing) nomenclature framework
Persistence of Touch DNA for Forensic Analysis
Population Genetic Issues for Forensic DNA Profiles
Efficient and Effective SNP System for Analysis of Highly Degraded DNA Samples
Develop non-PCR-based target enrichment reagents and methods for MPS analysis of forensic DNA
Statistical evaluation of forensic sequencing profiles
Genetic distance to improve human identification from the skin microbiome
New Methods for Next-Generation Sequencing Analysis of Damaged and Mixed DNA Samples
Identifying individuals through next generation DNA sequencing may involve degraded or mixed samples. A researcher has developed a technique to make fragmented DNA more readable, and a method to help pull individual profiles from mixed samples.
Embracing Next Generation Methods for Forensic DNA Sequence Analysis
The regions of the genome relied on for identification of individuals pose challenges for analysts because they often produce artifacts during processing. NIJ-funded research has led to a solution that lessens the artifact problem.