Method for detecting chromosome abnormality and recombinant site DNA sequence
A DNA sequence and recombination site technology, applied in biochemical equipment and methods, microbial measurement/inspection, etc., can solve problems such as sequencing chromosomal recombination at low cost, and achieve the effect of overcoming the short read length of NGS and reducing the cost of sequencing
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Embodiment 1
[0045] (1) Use classic karyotype analysis, FISH, BioNano and other techniques to determine the status of chromosomal abnormalities (including on which chromosome, what kind of abnormality, and approximate location), such as figure 1 As shown, the chromosomal abnormality is a chromosomal inversion.
[0046] Locate the approximate region of the chromosomal inversion site (such as the region of 1-5M).
[0047] (2) Design the sorted sgRNA sequence for this region, and prepare sgRNA in vitro.
[0048] (3) Extract chromosomal DNA; according to CRISPR technology, use Cas9 with single enzyme cutting activity (such as D10A or H840A) to cut the chromosome in vitro.
[0049] (4) Inactivate the Cas9 enzyme, and use DNA gap translation technology to incorporate base analogs (such as Biotin-modified dGTP) at the gap.
[0050] (5) DNA is randomly interrupted; the double strand is unwound into single-stranded DNA, and the single-stranded DNA is purified using the characteristics of base ana...
Embodiment 2
[0055] (1) Use classic karyotype analysis, FISH, BioNano and other techniques to determine the status of chromosomal abnormalities (including on which chromosome, what kind of abnormality, and approximate location), such as figure 2 As shown, the chromosomal abnormality is an interchromosomal translocation.
[0056] Locate the approximate region of the chromosomal inversion site (such as the region of 1-5M).
[0057] (2) Design and sort the sgRNA sequence for the c1 region of the first chromosome, and prepare the sgRNA in vitro.
[0058] (3) Extract chromosomal DNA; according to CRISPR technology, use Cas9 with single enzyme cutting activity (such as D10A or H840A) to cut the chromosome in vitro.
[0059] (4) Inactivate the Cas9 enzyme, and use DNA gap translation technology to incorporate base analogs (such as Biotin-modified dGTP) at the gap.
[0060] (5) DNA is randomly interrupted; the double strand is unwound into single-stranded DNA, and the single-stranded DNA is purif...
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