MX2018013085A - Analisis mutacional de adn de plasma para la deteccion de cancer. - Google Patents
Analisis mutacional de adn de plasma para la deteccion de cancer.Info
- Publication number
- MX2018013085A MX2018013085A MX2018013085A MX2018013085A MX2018013085A MX 2018013085 A MX2018013085 A MX 2018013085A MX 2018013085 A MX2018013085 A MX 2018013085A MX 2018013085 A MX2018013085 A MX 2018013085A MX 2018013085 A MX2018013085 A MX 2018013085A
- Authority
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- Mexico
- Prior art keywords
- door
- cancer
- level
- variant
- parameter
- Prior art date
Links
- 206010028980 Neoplasm Diseases 0.000 title abstract 7
- 201000011510 cancer Diseases 0.000 title abstract 5
- 238000001514 detection method Methods 0.000 title 1
- 230000000869 mutational effect Effects 0.000 title 1
- 230000000903 blocking effect Effects 0.000 abstract 4
- 206010069754 Acquired gene mutation Diseases 0.000 abstract 2
- 239000012472 biological sample Substances 0.000 abstract 2
- 238000012544 monitoring process Methods 0.000 abstract 2
- 238000012216 screening Methods 0.000 abstract 2
- 210000002966 serum Anatomy 0.000 abstract 2
- 230000037439 somatic mutation Effects 0.000 abstract 2
- 230000005540 biological transmission Effects 0.000 abstract 1
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- C—CHEMISTRY; METALLURGY
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- C12Q1/00—Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions
- C12Q1/68—Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions involving nucleic acids
- C12Q1/6876—Nucleic acid products used in the analysis of nucleic acids, e.g. primers or probes
- C12Q1/6883—Nucleic acid products used in the analysis of nucleic acids, e.g. primers or probes for diseases caused by alterations of genetic material
- C12Q1/6886—Nucleic acid products used in the analysis of nucleic acids, e.g. primers or probes for diseases caused by alterations of genetic material for cancer
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- C12Q1/00—Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions
- C12Q1/68—Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions involving nucleic acids
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- B01J19/00—Chemical, physical or physico-chemical processes in general; Their relevant apparatus
- B01J19/0046—Sequential or parallel reactions, e.g. for the synthesis of polypeptides or polynucleotides; Apparatus and devices for combinatorial chemistry or for making molecular arrays
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- C12N15/00—Mutation or genetic engineering; DNA or RNA concerning genetic engineering, vectors, e.g. plasmids, or their isolation, preparation or purification; Use of hosts therefor
- C12N15/09—Recombinant DNA-technology
- C12N15/10—Processes for the isolation, preparation or purification of DNA or RNA
- C12N15/1034—Isolating an individual clone by screening libraries
- C12N15/1065—Preparation or screening of tagged libraries, e.g. tagged microorganisms by STM-mutagenesis, tagged polynucleotides, gene tags
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- C12Q1/00—Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions
- C12Q1/68—Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions involving nucleic acids
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- C12Q1/00—Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions
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- C12Q1/00—Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions
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- C12Q1/6844—Nucleic acid amplification reactions
- C12Q1/6853—Nucleic acid amplification reactions using modified primers or templates
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- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
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- G01N33/48—Biological material, e.g. blood, urine; Haemocytometers
- G01N33/50—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing
- G01N33/53—Immunoassay; Biospecific binding assay; Materials therefor
- G01N33/574—Immunoassay; Biospecific binding assay; Materials therefor for cancer
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- G—PHYSICS
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- 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
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- G16B30/00—ICT specially adapted for sequence analysis involving nucleotides or amino acids
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- G16B30/00—ICT specially adapted for sequence analysis involving nucleotides or amino acids
- G16B30/10—Sequence alignment; Homology search
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- C12Q2525/00—Reactions involving modified oligonucleotides, nucleic acids, or nucleotides
- C12Q2525/10—Modifications characterised by
- C12Q2525/191—Modifications characterised by incorporating an adaptor
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- C12Q2535/00—Reactions characterised by the assay type for determining the identity of a nucleotide base or a sequence of oligonucleotides
- C12Q2535/122—Massive parallel sequencing
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- C12Q2537/16—Assays for determining copy number or wherein the copy number is of special importance
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- C12Q2600/00—Oligonucleotides characterized by their use
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- C12Q2600/00—Oligonucleotides characterized by their use
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- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02A—TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE
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Abstract
La presente invención se refiere a una frecuencia de mutaciones somáticas en una muestra biológica (por ejemplo, plasma o suero) de un sujeto sometido a la detección o monitoreo de cáncer, que se puede comparar con la del ADN constitucional del mismo sujeto. Un parámetro puede derivarse de estas frecuencias y utilizar para determinar una clasificación de un nivel de cáncer. Los falsos positivos pueden ser filtrados requiriendo que algún locus variante tenga al menos un número especificado de lecturas de secuencia variante (marcas), proporcionando así un parámetro más preciso. Las frecuencias relativas para los diferentes loci variantes pueden ser analizadas para determinar un nivel de heterogeneidad de los tumores en un paciente.
Applications Claiming Priority (5)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US201261662878P | 2012-06-21 | 2012-06-21 | |
US201261682725P | 2012-08-13 | 2012-08-13 | |
US201261695795P | 2012-08-31 | 2012-08-31 | |
US201261711172P | 2012-10-08 | 2012-10-08 | |
US13/801,748 US11261494B2 (en) | 2012-06-21 | 2013-03-13 | Method of measuring a fractional concentration of tumor DNA |
Publications (1)
Publication Number | Publication Date |
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MX2018013085A true MX2018013085A (es) | 2021-11-16 |
Family
ID=52274459
Family Applications (3)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
MX2014016058A MX360264B (es) | 2012-06-21 | 2013-06-14 | Analisis mutacional de adn de plasma para la deteccion de cancer. |
MX2018013085A MX2018013085A (es) | 2012-06-21 | 2014-12-19 | Analisis mutacional de adn de plasma para la deteccion de cancer. |
MX2023001154A MX2023001154A (es) | 2012-06-21 | 2014-12-19 | Analisis mutacional de adn de plasma para la deteccion de cancer. |
Family Applications Before (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
MX2014016058A MX360264B (es) | 2012-06-21 | 2013-06-14 | Analisis mutacional de adn de plasma para la deteccion de cancer. |
Family Applications After (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
MX2023001154A MX2023001154A (es) | 2012-06-21 | 2014-12-19 | Analisis mutacional de adn de plasma para la deteccion de cancer. |
Country Status (19)
Country | Link |
---|---|
US (3) | US11261494B2 (es) |
EP (3) | EP3456843B1 (es) |
JP (4) | JP6371280B2 (es) |
KR (6) | KR102656030B1 (es) |
CN (3) | CN107779506B (es) |
AU (4) | AU2013278994C1 (es) |
CA (2) | CA3080937A1 (es) |
DK (2) | DK2864501T3 (es) |
EA (2) | EA037292B1 (es) |
ES (2) | ES2894479T3 (es) |
HK (3) | HK1204013A1 (es) |
HU (1) | HUE056915T2 (es) |
IL (5) | IL311127A (es) |
MX (3) | MX360264B (es) |
PT (1) | PT3456843T (es) |
SG (2) | SG11201408113QA (es) |
TW (4) | TW202328458A (es) |
WO (1) | WO2013190441A2 (es) |
ZA (1) | ZA201409281B (es) |
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EP3572528A1 (en) | 2010-09-24 | 2019-11-27 | The Board of Trustees of the Leland Stanford Junior University | Direct capture, amplification and sequencing of target dna using immobilized primers |
KR20140024270A (ko) | 2010-12-30 | 2014-02-28 | 파운데이션 메디신 인코포레이티드 | 종양 샘플의 다유전자 분석의 최적화 |
US9892230B2 (en) | 2012-03-08 | 2018-02-13 | The Chinese University Of Hong Kong | Size-based analysis of fetal or tumor DNA fraction in plasma |
US11261494B2 (en) | 2012-06-21 | 2022-03-01 | The Chinese University Of Hong Kong | Method of measuring a fractional concentration of tumor DNA |
US20150011396A1 (en) | 2012-07-09 | 2015-01-08 | Benjamin G. Schroeder | Methods for creating directional bisulfite-converted nucleic acid libraries for next generation sequencing |
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DE202013012824U1 (de) | 2012-09-04 | 2020-03-10 | Guardant Health, Inc. | Systeme zum Erfassen von seltenen Mutationen und einer Kopienzahlvariation |
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KR102441391B1 (ko) * | 2014-07-25 | 2022-09-07 | 유니버시티 오브 워싱톤 | 무세포 dna를 생성하는 조직 및/또는 세포 유형을 결정하는 방법 및 이를 사용하여 질환 또는 장애를 확인하는 방법 |
CA2957633A1 (en) * | 2014-08-06 | 2016-02-11 | Nugen Technologies, Inc. | Digital measurements from targeted sequencing |
PL3198026T3 (pl) * | 2014-08-07 | 2020-05-18 | Pharmassist Ltd | Metody określania mutacji genu pik3ca w próbce |
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