Patent · US Active

Diagnosing cancer using genomic sequencing

US9121069B2 · kind B2 · utility

124Cited by
23References
29Claims
0Family size

Assignee

Inventors

Key dates

Filing dateJul 8, 2013
Grant dateSep 1, 2015
Priority date
Expiry dateJul 8, 2033

Classification

  • Technology area (CPC C)Chemistry; Metallurgy
  • CPC primaryC12Q2600/156
  • WIPO fieldBiotechnology
  • WIPO sectorChemistry

Abstract

Methods, systems, and apparatus determine whether a first chromosomal region exhibits a deletion or an amplification associated with cancer in a sample from a subject (e.g., where the sample includes a mixture of cell-free DNA from tumor cells and non-malignant cells. Nucleic acid molecules of the biological sample are sequenced. Respective amounts of a clinically-relevant chromosomal region and of background chromosomal region(s) are determined from results of the sequencing. A parameter derived from these amounts (e.g. a ratio) is compared to one or more cutoff values, thereby determining a classification of whether first chromosomal region exhibits a deletion or an amplification associated with cancer.

Source: USPTO / EPO open patent data. Objective bibliographic and citation counts.