WO2011140187A3 - Detecting chromosomal rearrangement - Google Patents
Detecting chromosomal rearrangement Download PDFInfo
- Publication number
- WO2011140187A3 WO2011140187A3 PCT/US2011/035135 US2011035135W WO2011140187A3 WO 2011140187 A3 WO2011140187 A3 WO 2011140187A3 US 2011035135 W US2011035135 W US 2011035135W WO 2011140187 A3 WO2011140187 A3 WO 2011140187A3
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- chromosomal rearrangement
- subject
- nucleic acid
- acid sequences
- labeled nucleic
- Prior art date
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Classifications
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- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12Q—MEASURING OR TESTING PROCESSES INVOLVING ENZYMES, NUCLEIC ACIDS OR MICROORGANISMS; COMPOSITIONS OR TEST PAPERS THEREFOR; PROCESSES OF PREPARING SUCH COMPOSITIONS; CONDITION-RESPONSIVE CONTROL IN MICROBIOLOGICAL OR ENZYMOLOGICAL PROCESSES
- 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
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12Q—MEASURING OR TESTING PROCESSES INVOLVING ENZYMES, NUCLEIC ACIDS OR MICROORGANISMS; COMPOSITIONS OR TEST PAPERS THEREFOR; PROCESSES OF PREPARING SUCH COMPOSITIONS; CONDITION-RESPONSIVE CONTROL IN MICROBIOLOGICAL OR ENZYMOLOGICAL PROCESSES
- C12Q2600/00—Oligonucleotides characterized by their use
- C12Q2600/16—Primer sets for multiplex assays
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- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Health & Medical Sciences (AREA)
- Organic Chemistry (AREA)
- Proteomics, Peptides & Aminoacids (AREA)
- Engineering & Computer Science (AREA)
- Immunology (AREA)
- Pathology (AREA)
- Analytical Chemistry (AREA)
- Zoology (AREA)
- Genetics & Genomics (AREA)
- Wood Science & Technology (AREA)
- Physics & Mathematics (AREA)
- Biotechnology (AREA)
- Microbiology (AREA)
- Molecular Biology (AREA)
- Hospice & Palliative Care (AREA)
- Biophysics (AREA)
- Oncology (AREA)
- Biochemistry (AREA)
- Bioinformatics & Cheminformatics (AREA)
- General Engineering & Computer Science (AREA)
- General Health & Medical Sciences (AREA)
- Measuring Or Testing Involving Enzymes Or Micro-Organisms (AREA)
Abstract
Provided herein are methods of detecting a chromosomal rearrangement in a subject. The methods comprise isolating deoxyribonucleic acid (DNA) comprising a target DNA sequence from a biological sample from the subject; performing a multiplex PCR assay comprising at least five primer pairs to the targeted DNA sequence, wherein the multiplex PCR assay produces a plurality of labeled nucleic acid sequences; contacting an array with the plurality of labeled nucleic acid sequences; and detecting a binding pattern of the labeled nucleic acid sequences to the array. The binding pattern indicates the presence or absence of a chromosomal rearrangement in the subject.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US33112410P | 2010-05-04 | 2010-05-04 | |
US61/331,124 | 2010-05-04 |
Publications (2)
Publication Number | Publication Date |
---|---|
WO2011140187A2 WO2011140187A2 (en) | 2011-11-10 |
WO2011140187A3 true WO2011140187A3 (en) | 2012-03-01 |
Family
ID=44904448
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/US2011/035135 WO2011140187A2 (en) | 2010-05-04 | 2011-05-04 | Detecting chromosomal rearrangement |
Country Status (1)
Country | Link |
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WO (1) | WO2011140187A2 (en) |
Families Citing this family (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US9084456B1 (en) * | 2012-05-28 | 2015-07-21 | Jack Zemer | Linkage for jewelry components |
US20150176077A1 (en) * | 2012-07-27 | 2015-06-25 | Inserm (Institut National De La Sante Et De La Recherche Medicale) | Methods for predicting whether a subject is at risk of developing a follicular lymphoma |
WO2014137329A1 (en) * | 2013-03-05 | 2014-09-12 | Agilent Technologies, Inc. | Synthesis of pools of probes by primer extension |
WO2015075196A1 (en) * | 2013-11-21 | 2015-05-28 | Assistance Publique - Hopitaux De Paris | Method for detecting chromosomal rearrangements |
CN105063032A (en) * | 2015-08-14 | 2015-11-18 | 深圳市瀚海基因生物科技有限公司 | Multiple PCR primers and method for constructing leukemia minimal residual disease BCR library based on high-flux sequencing |
CN105483256A (en) * | 2015-12-30 | 2016-04-13 | 广州安必平医药科技股份有限公司 | BCR gene and ABL gene detection probe, preparation method thereof and reagent kit |
CN107022602A (en) * | 2016-02-02 | 2017-08-08 | 生物梅里埃公司 | A kind of method of detection ALK genetic recombination |
GB201709675D0 (en) | 2017-06-16 | 2017-08-02 | Inivata Ltd | Method for detecting genomic rearrangements |
CN108048571A (en) * | 2017-12-29 | 2018-05-18 | 天津协和华美医学诊断技术有限公司 | A kind of detection kit for detecting CML related gene groups |
EP3833783A1 (en) | 2018-08-08 | 2021-06-16 | Inivata Ltd. | Method of sequencing using variable replicate multiplex pcr |
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2011
- 2011-05-04 WO PCT/US2011/035135 patent/WO2011140187A2/en active Application Filing
Non-Patent Citations (6)
Title |
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DE LELLIS, L. ET AL.: "Analysis of extended genomic rearrangements in oncological research.", ANNALS OF ONCOLOGY, vol. 18, no. 6, June 2007 (2007-06-01), pages VI173 - 178 * |
GORELLO, P. ET AL.: "Combined interphase fluorescence in situ hybridization elucidates the genetic heterogeneity of T-cell acute lymphoblastic leukemia in adults.", HEMATOLOGICA, vol. 95, no. 1, January 2010 (2010-01-01), pages 79 - 86 * |
MITYAEVA, O.N. ET AL: "Analysis of chromosomal translocation involving MML by hybridization with an oligonucleotide microarray", MOLECULAR BIOLOGY, vol. 38, no. 3, May 2004 (2004-05-01) - June 2004 (2004-06-01), pages 376 - 382 * |
NASEDKINA, R. V. ET AL.: "Clinical screening of gene rearrangements in childhood leukemia by using a multiplex polymerase chain reaction-microarray approach.", CLINICAL CANCER RESEARCH, vol. 9, 3 December 2003 (2003-12-03), pages 5620 - 5629, XP002458852 * |
RAILE, K. ET AL.: "HNF1 abnormality (mature-onset diabetes of the young 5) in children and adolescents.", DIABETES CARE, vol. 31, no. 11, November 2008 (2008-11-01), pages E83 * |
SPENCE, J. M. ET AL.: "Demonstration of array-based analysis for highly multiplexed PCR assays application to detection of IGH@-BCL2 translocations in FFPE follicular lymphoma specimens.", JOURNAL OF MOLECULAR DIAGNOSITICS, vol. 13, no. 3, 22 April 2011 (2011-04-22), pages 252 - 262 * |
Also Published As
Publication number | Publication date |
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WO2011140187A2 (en) | 2011-11-10 |
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