MX363345B - Determinación de genomas fetales para embarazos de múltiples fetos. - Google Patents
Determinación de genomas fetales para embarazos de múltiples fetos.Info
- Publication number
- MX363345B MX363345B MX2015010785A MX2015010785A MX363345B MX 363345 B MX363345 B MX 363345B MX 2015010785 A MX2015010785 A MX 2015010785A MX 2015010785 A MX2015010785 A MX 2015010785A MX 363345 B MX363345 B MX 363345B
- Authority
- MX
- Mexico
- Prior art keywords
- maternal
- inheritance
- paternal
- loci
- haplotype
- Prior art date
Links
Classifications
-
- 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
-
- 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
-
- 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
-
- 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
- C12Q2600/156—Polymorphic or mutational markers
-
- 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
Landscapes
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Proteomics, Peptides & Aminoacids (AREA)
- Health & Medical Sciences (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Analytical Chemistry (AREA)
- Physics & Mathematics (AREA)
- Zoology (AREA)
- Wood Science & Technology (AREA)
- Genetics & Genomics (AREA)
- Bioinformatics & Cheminformatics (AREA)
- General Health & Medical Sciences (AREA)
- Biotechnology (AREA)
- Biophysics (AREA)
- Immunology (AREA)
- Biochemistry (AREA)
- Microbiology (AREA)
- Molecular Biology (AREA)
- General Engineering & Computer Science (AREA)
- Pathology (AREA)
- Spectroscopy & Molecular Physics (AREA)
- Evolutionary Biology (AREA)
- Bioinformatics & Computational Biology (AREA)
- Medical Informatics (AREA)
- Theoretical Computer Science (AREA)
- Measuring Or Testing Involving Enzymes Or Micro-Organisms (AREA)
- Management, Administration, Business Operations System, And Electronic Commerce (AREA)
- Investigating Or Analysing Biological Materials (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201361789992P | 2013-03-15 | 2013-03-15 | |
| PCT/CN2014/073506 WO2014139477A1 (en) | 2013-03-15 | 2014-03-17 | Determining fetal genomes for multiple fetus pregnancies |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| MX2015010785A MX2015010785A (es) | 2015-11-26 |
| MX363345B true MX363345B (es) | 2019-03-20 |
Family
ID=51535879
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| MX2015010785A MX363345B (es) | 2013-03-15 | 2014-03-17 | Determinación de genomas fetales para embarazos de múltiples fetos. |
Country Status (11)
| Country | Link |
|---|---|
| US (1) | US10106836B2 (https=) |
| EP (2) | EP2971126B1 (https=) |
| JP (1) | JP2016518811A (https=) |
| KR (1) | KR20150132216A (https=) |
| CN (1) | CN105121660B (https=) |
| AU (1) | AU2014231358A1 (https=) |
| CA (1) | CA2901773A1 (https=) |
| EA (1) | EA201500939A1 (https=) |
| MX (1) | MX363345B (https=) |
| TW (1) | TWI637058B (https=) |
| WO (1) | WO2014139477A1 (https=) |
Families Citing this family (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP3783110B1 (en) | 2009-11-05 | 2022-11-23 | The Chinese University Of Hong Kong | Fetal genomic analysis from a maternal biological sample |
| CA2827873C (en) | 2011-02-24 | 2022-08-16 | The Chinese University Of Hong Kong | Molecular testing of multiple pregnancies |
| CN105121660B (zh) | 2013-03-15 | 2018-09-28 | 香港中文大学 | 确定多胎妊娠的胎儿基因组 |
| US10689706B2 (en) | 2015-07-20 | 2020-06-23 | The Chinese University Of Hong Kong | Methylation pattern analysis of haplotypes in tissues in a DNA mixture |
Family Cites Families (22)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB9704444D0 (en) | 1997-03-04 | 1997-04-23 | Isis Innovation | Non-invasive prenatal diagnosis |
| US6927028B2 (en) | 2001-08-31 | 2005-08-09 | Chinese University Of Hong Kong | Non-invasive methods for detecting non-host DNA in a host using epigenetic differences between the host and non-host DNA |
| US7727720B2 (en) | 2002-05-08 | 2010-06-01 | Ravgen, Inc. | Methods for detection of genetic disorders |
| EP1599608A4 (en) | 2003-03-05 | 2007-07-18 | Genetic Technologies Ltd | Identification of fetal DNA and fetal cell marker in maternal plasma or serum |
| ATE435301T1 (de) | 2003-10-16 | 2009-07-15 | Sequenom Inc | Nicht invasiver nachweis fötaler genetischer merkmale |
| US7645576B2 (en) | 2005-03-18 | 2010-01-12 | The Chinese University Of Hong Kong | Method for the detection of chromosomal aneuploidies |
| US20070122823A1 (en) | 2005-09-01 | 2007-05-31 | Bianchi Diana W | Amniotic fluid cell-free fetal DNA fragment size pattern for prenatal diagnosis |
| GB0523276D0 (en) | 2005-11-15 | 2005-12-21 | London Bridge Fertility | Chromosomal analysis by molecular karyotyping |
| EP3591068A1 (en) | 2006-02-02 | 2020-01-08 | The Board of Trustees of the Leland Stanford Junior University | Non-invasive fetal genetic screening by digital analysis |
| EP2351858B1 (en) | 2006-02-28 | 2014-12-31 | University of Louisville Research Foundation | Detecting fetal chromosomal abnormalities using tandem single nucleotide polymorphisms |
| EP2029779A4 (en) | 2006-06-14 | 2010-01-20 | Living Microsystems Inc | HIGHLY PARALLEL SNP GENOTYPING UTILIZATION FOR FETAL DIAGNOSIS |
| PL2557520T3 (pl) | 2007-07-23 | 2021-10-11 | The Chinese University Of Hong Kong | Określanie zaburzenia równowagi sekwencji kwasu nukleinowego |
| US12180549B2 (en) | 2007-07-23 | 2024-12-31 | The Chinese University Of Hong Kong | Diagnosing fetal chromosomal aneuploidy using genomic sequencing |
| EP2321642B1 (en) | 2008-08-04 | 2017-01-11 | Natera, Inc. | Methods for allele calling and ploidy calling |
| KR101781147B1 (ko) | 2008-12-22 | 2017-10-10 | 셀루라 인코포레이티드 | 대립유전자, 게놈 및 전사체 검출을 위한 방법 및 유전자형 분석 패널 |
| EP3783110B1 (en) * | 2009-11-05 | 2022-11-23 | The Chinese University Of Hong Kong | Fetal genomic analysis from a maternal biological sample |
| CA2780016C (en) | 2009-11-06 | 2017-09-19 | The Chinese University Of Hong Kong | Size-based genomic analysis |
| US9260745B2 (en) * | 2010-01-19 | 2016-02-16 | Verinata Health, Inc. | Detecting and classifying copy number variation |
| WO2011146632A1 (en) | 2010-05-18 | 2011-11-24 | Gene Security Network Inc. | Methods for non-invasive prenatal ploidy calling |
| US20120190020A1 (en) * | 2011-01-25 | 2012-07-26 | Aria Diagnostics, Inc. | Detection of genetic abnormalities |
| CA2827873C (en) * | 2011-02-24 | 2022-08-16 | The Chinese University Of Hong Kong | Molecular testing of multiple pregnancies |
| CN105121660B (zh) | 2013-03-15 | 2018-09-28 | 香港中文大学 | 确定多胎妊娠的胎儿基因组 |
-
2014
- 2014-03-17 CN CN201480012432.2A patent/CN105121660B/zh active Active
- 2014-03-17 EP EP14764129.4A patent/EP2971126B1/en not_active Not-in-force
- 2014-03-17 MX MX2015010785A patent/MX363345B/es unknown
- 2014-03-17 CA CA2901773A patent/CA2901773A1/en not_active Abandoned
- 2014-03-17 EP EP18194883.7A patent/EP3434790A1/en not_active Withdrawn
- 2014-03-17 WO PCT/CN2014/073506 patent/WO2014139477A1/en not_active Ceased
- 2014-03-17 JP JP2015561932A patent/JP2016518811A/ja active Pending
- 2014-03-17 EA EA201500939A patent/EA201500939A1/ru unknown
- 2014-03-17 KR KR1020157027071A patent/KR20150132216A/ko not_active Withdrawn
- 2014-03-17 AU AU2014231358A patent/AU2014231358A1/en not_active Abandoned
- 2014-03-17 TW TW103109991A patent/TWI637058B/zh active
- 2014-03-17 US US14/216,405 patent/US10106836B2/en not_active Expired - Fee Related
Also Published As
| Publication number | Publication date |
|---|---|
| CA2901773A1 (en) | 2014-09-18 |
| WO2014139477A1 (en) | 2014-09-18 |
| EP2971126A4 (en) | 2016-10-26 |
| EP2971126B1 (en) | 2018-11-07 |
| TWI637058B (zh) | 2018-10-01 |
| AU2014231358A1 (en) | 2015-09-24 |
| MX2015010785A (es) | 2015-11-26 |
| CN105121660A (zh) | 2015-12-02 |
| US10106836B2 (en) | 2018-10-23 |
| TW201441373A (zh) | 2014-11-01 |
| JP2016518811A (ja) | 2016-06-30 |
| KR20150132216A (ko) | 2015-11-25 |
| EA201500939A1 (ru) | 2016-01-29 |
| EP3434790A1 (en) | 2019-01-30 |
| US20140315200A1 (en) | 2014-10-23 |
| CN105121660B (zh) | 2018-09-28 |
| EP2971126A1 (en) | 2016-01-20 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| Hanna et al. | Pervasive polymorphic imprinted methylation in the human placenta | |
| Docherty et al. | Genome-wide DNA methylation analysis of patients with imprinting disorders identifies differentially methylated regions associated with novel candidate imprinted genes | |
| CY1121828T1 (el) | Αναλυση βασει μεγεθους θραυσματος εμβρυϊκου dna στο μητρικο πλασμα | |
| AU2010315037A8 (en) | Fetal genomic analysis from a maternal biological sample | |
| CY1117574T1 (el) | Αναλυση γονιδιωματικων κλασματων με χρηση των αριθμων πολυμορφισμων | |
| TW201129736A (en) | Size-based genomic analysis | |
| WO2010045617A9 (en) | Detecting genetic abnormalities | |
| MX363345B (es) | Determinación de genomas fetales para embarazos de múltiples fetos. | |
| WO2013177581A3 (en) | Whole genome sequencing of a human fetus | |
| MY208464A (en) | Universal haplotype-based noninvasive prenatal testing for single gene diseases | |
| Çağlayan et al. | ALPK3 gene mutation in a patient with congenital cardiomyopathy and dysmorphic features | |
| BR112012018458A2 (pt) | métodos e composições para diagnóstico pré-natal não invasivo de aneuploidias fetais | |
| WO2014165267A3 (en) | Systems and methods for prenatal genetic analysis | |
| JP2014507158A5 (https=) | ||
| SA518391141B1 (ar) | جزء جنيني من خلال تكوين متواليات ذات عمق سطحي | |
| Zhang et al. | Association of 14 bp insertion/deletion polymorphism of the HLA‐G gene in father with severe preeclampsia in Chinese | |
| WO2012038382A3 (en) | Markers for joint displasia, osteoarthritis and conditions secondary thereto | |
| JP2014513958A5 (https=) | ||
| JP2016518811A5 (https=) | ||
| Pio et al. | A novel mutation in intron 11 donor splice site, responsible of a rare genotype in thyroglobulin gene by altering the pre-mRNA splincing process. Cell expression and bioinformatic analysis | |
| RU2012100987A (ru) | Способ прогнозирования отслойки хориона и плаценты на ранних сроках беременности на основании определения полиморфизма генов ингибитора активатора плазминогена i типа (pai-1) | |
| WO2011146788A3 (en) | Methods of assessing a risk of developing necrotizing meningoencephalitis | |
| Duan et al. | Association analysis of GWAS hits and non-syndromic cleft lip with/without palate with cleft alveolar in Han population of western China | |
| Yin et al. | Fine-mapping markers of lung cancer susceptibility in a sub-region of chromosome 19q13. 3 among Chinese | |
| ZHU et al. | Prenatal diagnosis of fetal β-thalassemia gene for the couples carried with the β-thalassemia gene in Huizhou city. |