Supported by a 2013 National Institute of Justice grant, this research investigated a suite of DNA artifact problems by developing a method for isolating, enriching, and sequencing Short Tandem Repeats (STRs). The research began by using CRISPR-Cas9 technology, a powerful molecular tool that allows scientists to cut DNA molecules at any location, and designing probes that align to the flanking regions of the targeted STRs. This aspect allowed the research team to cut out full STRs, attach unique molecular tags, and isolate them before sequencing. The researchers were able to sequence the STR fragments successfully without amplifying them beforehand, thus dramatically reducing the introduction of stutter artifacts. The regions of the genome relied on for identification of individuals pose challenges for analysts because they often produce artifacts during processing.
Downloads
Similar Publications
- Extraction of Ignitable Liquid Residues by Dynamic Capillary Headspace Sampling and Comparison to the Carbon Strip Method
- ILIAD: A Suite of Automated Snakemake Workflows for Processing Genomic Data for Downstream Applications
- Environmental Predictors Impact Microbial-based Postmortem Interval (PMI) Estimation Models within Human Decomposition Soils