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INTERPOL HANDBOOK ON DNA DATA EXCHANGE AND PRACTICE

INTERPOL HANDBOOK ON DNA DATA EXCHANGE AND PRACTICE

INTERPOL HANDBOOK ON DNA DATA EXCHANGE AND PRACTICE

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Detail of Step 4-Figure 1 - Separation and visualization of the <strong>DNA</strong> profileRoutine forensic <strong>DNA</strong> profiling targets markers on the <strong>DNA</strong> known as short tandemrepeats (or STRs). STRs first emerged as potential forensic markers in the early 1990sand quickly demonstrated important advantages as a forensic technique. In particular,their small molecular size meant the tests were more sensitive, requiring as little as0.2–0.5ng of <strong>DNA</strong>. This is 100 to 250 times more sensitive than the original <strong>DNA</strong>profiling techniques. This also meant that these loci had improved reliability when the<strong>DNA</strong> was highly degraded.Analysis of STRs has advanced to the point where up to 16 individual STR markersare combined into a single test. This technique (known as multiplexing) increases thediscriminating power of the <strong>DNA</strong> analysis without compromising the overall sensitivityof the test, or its suitability in the forensic context.year of release name no. of loci1997 AmpFlSTR Profiler Plus® 101998 AmpFlSTR COfiler® 71999 AmpFlSTR SGM Plus® 112001 AmpFlSTR Identifiler® 162001 PowerPlex® 16 16Table 3: STR multiplexes commonly used in forensic <strong>DNA</strong> profilingNote that we have three types of <strong>DNA</strong> analysis:1. Set of markers used for national <strong>DNA</strong> database that can provide identification of anindividual through direct comparison2. Markers such as Y-STRs and mt<strong>DNA</strong> that can exclude numerous people but may notbe sufficient for identification/individualisation in its own right3. Other markers that may assist investigators by providing an indication of aspectssuch as geographical origin, physical characteristics etc.IN THE LABORATORY PAGE 31

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