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  2. Low copy number - Wikipedia

    en.wikipedia.org/wiki/Low_copy_number

    Low Copy Number (LCN) is a DNA profiling technique developed by the UK Forensic Science Service (FSS) which has been in use since 1999. [1]In the United Kingdom use of the technique was suspended between 21 December 2007 and 14 January 2008 while the Crown Prosecution Service conducted a review into its use – this suspension has now been lifted.

  3. DNA footprinting - Wikipedia

    en.wikipedia.org/wiki/DNA_footprinting

    The DNA template with the protein will result in ladder distribution with a break in it, the "footprint", where the DNA has been protected from the cleavage agent. Note: Maxam-Gilbert chemical DNA sequencing can be run alongside the samples on the polyacrylamide gel to allow the prediction of the exact location of ligand binding site.

  4. DNA - Wikipedia

    en.wikipedia.org/wiki/DNA

    In DNA replication, DNA-dependent DNA polymerases make copies of DNA polynucleotide chains. To preserve biological information, it is essential that the sequence of bases in each copy are precisely complementary to the sequence of bases in the template strand.

  5. Genetic testing - Wikipedia

    en.wikipedia.org/wiki/Genetic_testing

    Genetic testing, also known as DNA testing, is used to identify changes in DNA sequence or chromosome structure. Genetic testing can also include measuring the results of genetic changes, such as RNA analysis as an output of gene expression , or through biochemical analysis to measure specific protein output. [ 1 ]

  6. Real-time polymerase chain reaction - Wikipedia

    en.wikipedia.org/wiki/Real-time_polymerase_chain...

    During the exponential amplification phase, the quantity of the target DNA template (amplicon) doubles every cycle. For example, a DNA sample whose C q precedes that of another sample by 3 cycles contained 2 3 = 8 times more template. However, the efficiency of amplification is often variable among primers and templates.

  7. Sanger sequencing - Wikipedia

    en.wikipedia.org/wiki/Sanger_sequencing

    Following rounds of template DNA extension from the bound primer, the resulting DNA fragments are heat denatured and separated by size using gel electrophoresis. In the original publication of 1977, [ 6 ] the formation of base-paired loops of ssDNA was a cause of serious difficulty in resolving bands at some locations.

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