18435880. Methods and Systems for Analyzing Nucleic Acid Molecules simplified abstract (The Board of Trustees of the Leland Stanford Junior University)
Contents
- 1 Methods and Systems for Analyzing Nucleic Acid Molecules
- 1.1 Organization Name
- 1.2 Inventor(s)
- 1.3 Methods and Systems for Analyzing Nucleic Acid Molecules - A simplified explanation of the abstract
- 1.4 Simplified Explanation
- 1.5 Potential Applications
- 1.6 Problems Solved
- 1.7 Benefits
- 1.8 Potential Commercial Applications
- 1.9 Possible Prior Art
- 1.10 Unanswered Questions
- 1.11 Original Abstract Submitted
Methods and Systems for Analyzing Nucleic Acid Molecules
Organization Name
The Board of Trustees of the Leland Stanford Junior University
Inventor(s)
David M. Kurtz of San Carlos CA (US)
Maximilian Diehn of San Carlos CA (US)
Arash Ash Alizadeh of San Mateo CA (US)
Methods and Systems for Analyzing Nucleic Acid Molecules - A simplified explanation of the abstract
This abstract first appeared for US patent application 18435880 titled 'Methods and Systems for Analyzing Nucleic Acid Molecules
Simplified Explanation
The patent application describes processes and materials for detecting cancer from a biopsy, including sequencing cell-free nucleic acids to detect sequences derived from a neoplasm.
- Cell-free nucleic acids can be sequenced to detect cancer.
- Detection of somatic variants can indicate the presence of cancer.
- Clinical intervention can be performed based on diagnostic scan results.
Potential Applications
The technology can be used in medical diagnostics to detect cancer at an early stage, allowing for timely clinical intervention.
Problems Solved
This technology helps in early detection of cancer, which can lead to better treatment outcomes and improved patient survival rates.
Benefits
- Early detection of cancer - Timely clinical intervention - Improved treatment outcomes
Potential Commercial Applications
The technology can be utilized by healthcare providers, diagnostic laboratories, and pharmaceutical companies for cancer detection and treatment monitoring.
Possible Prior Art
One possible prior art could be the use of next-generation sequencing technologies for cancer detection from biopsy samples.
Unanswered Questions
How cost-effective is this technology compared to existing methods for cancer detection?
Answer: The cost-effectiveness of this technology compared to existing methods needs to be further studied and evaluated to determine its economic feasibility for widespread adoption.
What are the potential limitations or challenges in implementing this technology in clinical settings?
Answer: The potential challenges in implementing this technology in clinical settings, such as regulatory approvals, data interpretation, and infrastructure requirements, need to be addressed for successful integration into routine medical practice.
Original Abstract Submitted
Processes and materials to detect cancer from a biopsy are described. In some cases, cell-free nucleic acids can be sequenced, and the sequencing result can be utilized to detect sequences derived from a neoplasm. Detection of somatic variants occurring in phase can indicate the presence of cancer in a diagnostic scan and a clinical intervention can be performed.
- The Board of Trustees of the Leland Stanford Junior University
- David M. Kurtz of San Carlos CA (US)
- Maximilian Diehn of San Carlos CA (US)
- Arash Ash Alizadeh of San Mateo CA (US)
- C12Q1/6886
- C12N15/10
- C12Q1/6869
- C12Q1/6874
- G16B20/00
- G16B20/10
- G16B20/20
- G16B30/00
- G16B30/10
- G16B35/20
- G16B40/00
- G16H10/40
- G16H20/10
- G16H50/20
- G16H50/30
- G16H50/70
- G16H70/60
- G16H10/60