Single nucleotide polymorphism (SNP)
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
Recent Developments in Y-short Tandem Repeat and Y-single Nucleotide Polymorphism Analysis
Developing a SNP Panel for Forensic Identification of Individuals
Highly Multiplexed Assays for Measuring Polymorphisms on the Y-chromosome
Sub-Populations Within the Major European and African Derived Haplogroups R1b3 and E3a are Differentiated by Previously Phylogenetically Undefined Y-SNPs
Characterization of mtDNA SNP Typing and Mixture Ratio Assessment With Simultaneous Real-Time PCR Quantification of Both Allelic States
Effective Strategies for Forensic Analysis in the Mitochondrial DNA Coding Region
Improved Analysis of DNA Short Tandem Repeats With Time-of-Flight Mass Spectrometry
Minimal SNP Overlap Among Multiple Panels of Ancestry informative Markers Argues for More International Collaboration
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.
Analysis of DNA From Post-blast Pipe Bomb Fragments for Identification and Determination of Ancestry
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.