EP4320618A4 - Zellfreies dna-sequenzdatenanalyseverfahren zur untersuchung des nukleosomschutzes und der chromatzugänglichkeit - Google Patents
Zellfreies dna-sequenzdatenanalyseverfahren zur untersuchung des nukleosomschutzes und der chromatzugänglichkeitInfo
- Publication number
- EP4320618A4 EP4320618A4 EP22785557.4A EP22785557A EP4320618A4 EP 4320618 A4 EP4320618 A4 EP 4320618A4 EP 22785557 A EP22785557 A EP 22785557A EP 4320618 A4 EP4320618 A4 EP 4320618A4
- Authority
- EP
- European Patent Office
- Prior art keywords
- investigating
- cell
- dna sequence
- data analysis
- analysis method
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Withdrawn
Links
Classifications
-
- G—PHYSICS
- G16—INFORMATION AND COMMUNICATION TECHNOLOGY [ICT] SPECIALLY ADAPTED FOR SPECIFIC APPLICATION FIELDS
- G16B—BIOINFORMATICS, i.e. INFORMATION AND COMMUNICATION TECHNOLOGY [ICT] SPECIALLY ADAPTED FOR GENETIC OR PROTEIN-RELATED DATA PROCESSING IN COMPUTATIONAL MOLECULAR BIOLOGY
- G16B20/00—ICT specially adapted for functional genomics or proteomics, e.g. genotype-phenotype associations
- G16B20/20—Allele or variant detection, e.g. single nucleotide polymorphism [SNP] detection
-
- G—PHYSICS
- G16—INFORMATION AND COMMUNICATION TECHNOLOGY [ICT] SPECIALLY ADAPTED FOR SPECIFIC APPLICATION FIELDS
- G16B—BIOINFORMATICS, i.e. INFORMATION AND COMMUNICATION TECHNOLOGY [ICT] SPECIALLY ADAPTED FOR GENETIC OR PROTEIN-RELATED DATA PROCESSING IN COMPUTATIONAL MOLECULAR BIOLOGY
- G16B25/00—ICT specially adapted for hybridisation; ICT specially adapted for gene or protein expression
- G16B25/10—Gene or protein expression profiling; Expression-ratio estimation or normalisation
-
- G—PHYSICS
- G16—INFORMATION AND COMMUNICATION TECHNOLOGY [ICT] SPECIALLY ADAPTED FOR SPECIFIC APPLICATION FIELDS
- G16B—BIOINFORMATICS, i.e. INFORMATION AND COMMUNICATION TECHNOLOGY [ICT] SPECIALLY ADAPTED FOR GENETIC OR PROTEIN-RELATED DATA PROCESSING IN COMPUTATIONAL MOLECULAR BIOLOGY
- G16B30/00—ICT specially adapted for sequence analysis involving nucleotides or amino acids
- G16B30/10—Sequence alignment; Homology search
-
- G—PHYSICS
- G16—INFORMATION AND COMMUNICATION TECHNOLOGY [ICT] SPECIALLY ADAPTED FOR SPECIFIC APPLICATION FIELDS
- G16B—BIOINFORMATICS, i.e. INFORMATION AND COMMUNICATION TECHNOLOGY [ICT] SPECIALLY ADAPTED FOR GENETIC OR PROTEIN-RELATED DATA PROCESSING IN COMPUTATIONAL MOLECULAR BIOLOGY
- G16B40/00—ICT specially adapted for biostatistics; ICT specially adapted for bioinformatics-related machine learning or data mining, e.g. knowledge discovery or pattern finding
- G16B40/20—Supervised data analysis
-
- G—PHYSICS
- G16—INFORMATION AND COMMUNICATION TECHNOLOGY [ICT] SPECIALLY ADAPTED FOR SPECIFIC APPLICATION FIELDS
- G16H—HEALTHCARE INFORMATICS, i.e. INFORMATION AND COMMUNICATION TECHNOLOGY [ICT] SPECIALLY ADAPTED FOR THE HANDLING OR PROCESSING OF MEDICAL OR HEALTHCARE DATA
- G16H20/00—ICT specially adapted for therapies or health-improving plans, e.g. for handling prescriptions, for steering therapy or for monitoring patient compliance
- G16H20/10—ICT specially adapted for therapies or health-improving plans, e.g. for handling prescriptions, for steering therapy or for monitoring patient compliance relating to drugs or medications, e.g. for ensuring correct administration to patients
-
- G—PHYSICS
- G16—INFORMATION AND COMMUNICATION TECHNOLOGY [ICT] SPECIALLY ADAPTED FOR SPECIFIC APPLICATION FIELDS
- G16H—HEALTHCARE INFORMATICS, i.e. INFORMATION AND COMMUNICATION TECHNOLOGY [ICT] SPECIALLY ADAPTED FOR THE HANDLING OR PROCESSING OF MEDICAL OR HEALTHCARE DATA
- G16H50/00—ICT specially adapted for medical diagnosis, medical simulation or medical data mining; ICT specially adapted for detecting, monitoring or modelling epidemics or pandemics
- G16H50/20—ICT specially adapted for medical diagnosis, medical simulation or medical data mining; ICT specially adapted for detecting, monitoring or modelling epidemics or pandemics for computer-aided diagnosis, e.g. based on medical expert systems
Landscapes
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Physics & Mathematics (AREA)
- Life Sciences & Earth Sciences (AREA)
- Medical Informatics (AREA)
- General Health & Medical Sciences (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Public Health (AREA)
- Biophysics (AREA)
- Spectroscopy & Molecular Physics (AREA)
- Theoretical Computer Science (AREA)
- Bioinformatics & Computational Biology (AREA)
- Biotechnology (AREA)
- Evolutionary Biology (AREA)
- Genetics & Genomics (AREA)
- Chemical & Material Sciences (AREA)
- Data Mining & Analysis (AREA)
- Epidemiology (AREA)
- Molecular Biology (AREA)
- Analytical Chemistry (AREA)
- Proteomics, Peptides & Aminoacids (AREA)
- Biomedical Technology (AREA)
- Primary Health Care (AREA)
- Databases & Information Systems (AREA)
- Artificial Intelligence (AREA)
- Evolutionary Computation (AREA)
- Software Systems (AREA)
- Medicinal Chemistry (AREA)
- Computer Vision & Pattern Recognition (AREA)
- Bioethics (AREA)
- Pathology (AREA)
- Measuring Or Testing Involving Enzymes Or Micro-Organisms (AREA)
- Investigating Or Analysing Biological Materials (AREA)
- Apparatus Associated With Microorganisms And Enzymes (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US202163172590P | 2021-04-08 | 2021-04-08 | |
| US202163276378P | 2021-11-05 | 2021-11-05 | |
| PCT/US2022/024082 WO2022217096A2 (en) | 2021-04-08 | 2022-04-08 | Cell-free dna sequence data analysis method to examine nucleosome protection and chromatin accessibility |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| EP4320618A2 EP4320618A2 (de) | 2024-02-14 |
| EP4320618A4 true EP4320618A4 (de) | 2025-08-27 |
Family
ID=83545807
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| EP22785557.4A Withdrawn EP4320618A4 (de) | 2021-04-08 | 2022-04-08 | Zellfreies dna-sequenzdatenanalyseverfahren zur untersuchung des nukleosomschutzes und der chromatzugänglichkeit |
Country Status (5)
| Country | Link |
|---|---|
| EP (1) | EP4320618A4 (de) |
| JP (1) | JP2024515565A (de) |
| AU (1) | AU2022255198A1 (de) |
| CA (1) | CA3214391A1 (de) |
| WO (1) | WO2022217096A2 (de) |
Families Citing this family (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN115376616B (zh) * | 2022-10-24 | 2023-04-28 | 臻和(北京)生物科技有限公司 | 一种基于cfDNA多组学的多分类方法及装置 |
| EP4665867A2 (de) * | 2023-02-13 | 2025-12-24 | Delfi Diagnostics, Inc. | Delfi-abgeleitete zellfreie dna-fragmentierungsmuster zur differenzierung histologischer subtypen von lungenkrebs auf nichtinvasive weise |
| US20250101528A1 (en) * | 2023-09-22 | 2025-03-27 | Centre For Novostics | Uses of cell-free dna fragmentation patterns associated with epigenetic modifications |
| AU2024357837A1 (en) * | 2023-10-13 | 2026-04-23 | Dana-Farber Cancer Institute, Inc. | Methods, kits and systems for determining the status of lung cancer and methods for treating lung cancer based on same |
| WO2025081100A1 (en) * | 2023-10-13 | 2025-04-17 | Precede Biosciences, Inc. | Methods, kits and systems for determining the her2 status of cancer and methods for treating cancer based on same |
| WO2025081094A2 (en) * | 2023-10-13 | 2025-04-17 | Precede Biosciences, Inc. | Methods, kits and systems for determining the er status of cancer and methods for treating cancer based on same |
| WO2025213034A1 (en) * | 2024-04-05 | 2025-10-09 | Predicine, Inc. | Systems and methods for multiple biomarker analysis in cancer |
| WO2025245302A1 (en) * | 2024-05-22 | 2025-11-27 | Precede Biosciences, Inc. | Methods, kits and systems for determining er activity of cancer and methods for treating cancer based on same |
| WO2025250678A1 (en) * | 2024-05-28 | 2025-12-04 | Genecentric Therapeutics, Inc. | Methods and systems for porting tissue-based classifiers into liquid biopsy samples |
Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20150005176A1 (en) * | 2013-06-21 | 2015-01-01 | Sequenom, Inc. | Methods and processes for non-invasive assessment of genetic variations |
| US20200087710A1 (en) * | 2017-03-17 | 2020-03-19 | Sequenom, Inc. | Methods and processes for assessment of genetic mosaicism |
Family Cites Families (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US8725422B2 (en) * | 2010-10-13 | 2014-05-13 | Complete Genomics, Inc. | Methods for estimating genome-wide copy number variations |
| US10497461B2 (en) * | 2012-06-22 | 2019-12-03 | Sequenom, Inc. | Methods and processes for non-invasive assessment of genetic variations |
| EP4358097A1 (de) * | 2014-07-25 | 2024-04-24 | University of Washington | Verfahren zur bestimmung von gewebe- und/oder zelltypen zur entstehung von zellfreier dna und verfahren zur identifizierung einer krankheit oder störung damit |
| US20190287645A1 (en) * | 2016-07-06 | 2019-09-19 | Guardant Health, Inc. | Methods for fragmentome profiling of cell-free nucleic acids |
| EP3635133A4 (de) * | 2017-06-09 | 2021-03-03 | Bellwether Bio, Inc. | Bestimmung des krebstyps bei einer person durch probabilistische modellierung von zirkulierenden nukleinsäurefragment-endpunkten |
| CN112805563B (zh) * | 2018-05-18 | 2025-06-13 | 约翰·霍普金斯大学 | 用于评估和/或治疗癌症的无细胞dna |
| JP7747524B2 (ja) * | 2019-05-14 | 2025-10-01 | テンパス エーアイ,インコーポレイテッド | マルチラベルがん分類のためのシステムおよび方法 |
-
2022
- 2022-04-08 EP EP22785557.4A patent/EP4320618A4/de not_active Withdrawn
- 2022-04-08 WO PCT/US2022/024082 patent/WO2022217096A2/en not_active Ceased
- 2022-04-08 CA CA3214391A patent/CA3214391A1/en active Pending
- 2022-04-08 AU AU2022255198A patent/AU2022255198A1/en not_active Abandoned
- 2022-04-08 JP JP2023561726A patent/JP2024515565A/ja active Pending
Patent Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20150005176A1 (en) * | 2013-06-21 | 2015-01-01 | Sequenom, Inc. | Methods and processes for non-invasive assessment of genetic variations |
| US20200087710A1 (en) * | 2017-03-17 | 2020-03-19 | Sequenom, Inc. | Methods and processes for assessment of genetic mosaicism |
Non-Patent Citations (2)
| Title |
|---|
| DOEBLEY ANNA-LISA ET AL: "A framework for clinical cancer subtyping from nucleosome profiling of cell-free DNA", NATURE COMMUNICATIONS, vol. 13, no. 1, 3 December 2022 (2022-12-03), UK, XP093292028, ISSN: 2041-1723, Retrieved from the Internet <URL:https://www.nature.com/articles/s41467-022-35076-w> DOI: 10.1038/s41467-022-35076-w * |
| Y. BENJAMINI ET AL: "Summarizing and correcting the GC content bias in high-throughput sequencing", NUCLEIC ACIDS RESEARCH, vol. 40, no. 10, 9 February 2012 (2012-02-09), pages 1 - 14, XP055162924, ISSN: 0305-1048, DOI: 10.1093/nar/gks001 * |
Also Published As
| Publication number | Publication date |
|---|---|
| WO2022217096A3 (en) | 2022-12-29 |
| WO2022217096A2 (en) | 2022-10-13 |
| AU2022255198A1 (en) | 2023-11-23 |
| JP2024515565A (ja) | 2024-04-10 |
| CA3214391A1 (en) | 2022-10-13 |
| EP4320618A2 (de) | 2024-02-14 |
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| RIC1 | Information provided on ipc code assigned before grant |
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