Sathyanarayana et al., 2022 - Google Patents
Applications of Long-Read Sequencing Technology in Clinical GenomicsSathyanarayana et al., 2022
- Document ID
- 13008119638889845799
- Author
- Sathyanarayana S
- Deharvengt S
- Huang G
- Barney R
- Shah P
- Lefferts J
- Publication year
- Publication venue
- Advances in Molecular Pathology
External Links
Snippet
Genetics and genomics research has constantly been guided by state-of-the-art sequencing technologies, which initially emerged from Sanger sequencing and were later followed by next-generation sequencing (NGS)[1]. NGS technology has transformed modern genetics …
- 238000005516 engineering process 0 title abstract description 25
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- C12Q1/00—Measuring or testing processes involving enzymes, nucleic acids or micro-organisms; Compositions therefor; Processes of preparing such compositions
- C12Q1/68—Measuring or testing processes involving enzymes, nucleic acids or micro-organisms; Compositions therefor; Processes of preparing such compositions involving nucleic acids
- C12Q1/6813—Hybridisation assays
- C12Q1/6827—Hybridisation assays for mutation or polymorphism detection
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- C12Q1/00—Measuring or testing processes involving enzymes, nucleic acids or micro-organisms; Compositions therefor; Processes of preparing such compositions
- C12Q1/68—Measuring or testing processes involving enzymes, nucleic acids or micro-organisms; Compositions therefor; Processes of preparing such compositions involving nucleic acids
- C12Q1/6876—Hybridisation probes
- C12Q1/6883—Hybridisation probes for diseases caused by alterations of genetic material
- C12Q1/6886—Hybridisation probes for diseases caused by alterations of genetic material for cancer
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- C12Q1/6844—Nucleic acid amplification reactions
- C12Q1/6846—Common amplification features
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- C12Q1/6869—Methods for sequencing
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- C12Q1/6802—General aspects
- C12Q1/6809—Sequence identification involving differential detection
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- G06F19/22—Bioinformatics, i.e. methods or systems for genetic or protein-related data processing in computational molecular biology for sequence comparison involving nucleotides or amino acids, e.g. homology search, motif or SNP [Single-Nucleotide Polymorphism] discovery or sequence alignment
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