http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-3959342-A1

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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12Q1-6858
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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12Q1-6883
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filingDate 2020-12-23-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_a3caab01a46c7da42908eb52d1817d67
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publicationDate 2022-03-02-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber EP-3959342-A1
titleOfInvention Methods and kits for the enrichment and detection of dna and rna modifications and functional motifs
abstract Provided herein are methods for mapping modified nucleotide residues in nucleic acids. The methods include providing a nucleic acid sample in which non-target or target modified and unmodified nucleotide residues are converted to form of a different nucleotide (such a "C" being converted to "T"). Second strand synthesis is then performed on the converted nucleic acids using a set of anchored-base primers. Each primer in the set of anchored-base primers comprises one or more anchor bases at the 3' terminus that are complementary to the target nucleotide (e.g., "G" or "CpG"), and a sequence of nucleotides selected from a set of sequences that could be a fully or partially degenerate set of sequences. For example, the sequence could be 5'-XnG-3' and/or 5'-X(n-1)CG-3', wherein X is any base, and n=2 to 25. Double-stranded nucleic acid products can be analyzed, for example by amplification and high throughput sequencing.
priorityDate 2019-12-23-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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