Method for identification and quantification of nucleic acid expression, splice variant, translocation, copy number, or methylation changes
US10344321B2 · kind B2 · utility
Assignee
Inventors
Key dates
| Filing date | Oct 8, 2015 |
| Grant date | Jul 9, 2019 |
| Priority date | — |
| Expiry date | Jan 26, 2036 |
Classification
- Technology area (CPC C)Chemistry; Metallurgy
- CPC primaryC12Q2600/156
- WIPO fieldBiotechnology
- WIPO sectorChemistry
Abstract
The present invention relates to methods and devices for identifying and quantifying, including low abundance, nucleotide base mutations, insertions, deletions, translocations, splice variants, miRNA variants, alternative transcripts, alternative start sites, alternative coding sequences, alternative non-coding sequences, alternative splicings, exon insertions, exon deletions, intron insertions, or other rearrangement at the genome level and/or methylated nucleotide bases.
Source: USPTO / EPO open patent data. Objective bibliographic and citation counts.