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  2. Minimally manipulated cells - Wikipedia

    en.wikipedia.org/wiki/Minimally_manipulated_cells

    The criteria of "minimal manipulation" are variative in different countries. European regulations, according to the Reflection Paper on the classification of advanced therapy medicinal products of the European Medicines Agency, define "minimal manipulation" as the procedure that does not change biological characteristics and functions of cells. [5]

  3. DNA shuffling - Wikipedia

    en.wikipedia.org/wiki/DNA_shuffling

    DNA shuffling has since been applied to generate libraries of hybrid or chimeric genes and has inspired family shuffling which is defined as the use of related genes in DNA shuffling. [ 17 ] [ 18 ] [ 19 ] Additionally, DNA shuffling has been applied to protein and small molecule pharmaceuticals, bioremediation, gene therapy, vaccines, and ...

  4. Off-target genome editing - Wikipedia

    en.wikipedia.org/wiki/Off-target_genome_editing

    These tools use different mechanisms to bind a predetermined sequence of DNA (“target”), which they cleave (or "cut"), creating a double-stranded chromosomal break (DSB) that summons the cell's DNA repair mechanisms (non-homologous end joining and homologous recombination ) and leads to site-specific modifications. [2]

  5. FLP-FRT recombination - Wikipedia

    en.wikipedia.org/wiki/FLP-FRT_recombination

    In genetics, Flp-FRT recombination is a site-directed recombination technology, increasingly used to manipulate an organism's DNA under controlled conditions in vivo.It is analogous to Cre-lox recombination but involves the recombination of sequences between short flippase recognition target (FRT) sites by the recombinase flippase (Flp) derived from the 2 μ plasmid of baker's yeast ...

  6. Gene targeting - Wikipedia

    en.wikipedia.org/wiki/Gene_targeting

    The two most established forms of gene editing are gene-targeting and targeted-mutagenesis. While gene targeting relies on the Homology Directed Repair (HDR) (also called Homologous Recombination , HR) DNA repair pathway, targeted-mutagenesis uses Non-Homologous-End-Joining (NHEJ) of broken DNA.

  7. No-SCAR genome editing - Wikipedia

    en.wikipedia.org/wiki/No-SCAR_genome_editing

    No-SCAR genome editing is an editing method that is able to manipulate the Escherichia coli (E. coli) genome.The system relies on recombineering whereby DNA sequences are combined and manipulated through homologous recombination.

  8. Orphan gene - Wikipedia

    en.wikipedia.org/wiki/Orphan_gene

    When homologous genes exist but are simply undetected, the emergence of these orphan genes can be explained by well-characterized phenomena such as genomic recombination, exon shuffling, gene duplication and divergence, etc. Orphan genes may also simply lack true homologues and in such cases have an independent origins via de novo gene birth ...

  9. Microhomology-mediated end joining - Wikipedia

    en.wikipedia.org/wiki/Microhomology-mediated_end...

    Microhomology-mediated end joining (MMEJ), also known as alternative nonhomologous end-joining (Alt-NHEJ) is one of the pathways for repairing double-strand breaks in DNA. As reviewed by McVey and Lee, [1] the foremost distinguishing property of MMEJ is the use of microhomologous sequences during the alignment of broken ends before joining, thereby resulting in deletions flanking the original ...