Non-invasive prenatal measurement of the fetal genome - Wikidata - awgldk - TriplyDB

Non-invasive prenatal measurement of the fetal genome

Non-invasive prenatal measurement of the fetal genome

http://www.wikidata.org/entity/Q34286073

about

Analysis of single nucleic acid molecules in micro- and nano-fluidics Understanding the Basics of NGS: From Mechanism to Variant Calling Impact of New Genomic Technologies on Understanding Adverse Drug Reactions High-throughput sequencing for biology and medicine Non-Invasive Prenatal Testing Using Cell Free DNA in Maternal Plasma: Recent Developments and Future Prospects Recent advances in prenatal genetic screening and testing Individualized medicine from prewomb to tomb Microelectromechanical systems and nephrology: the next frontier in renal replacement technology.Integrative methods for analyzing big data in precision medicine.Maternal plasma sequencing: a powerful tool towards fetal whole genome recovery.Noninvasive in vivo monitoring of tissue-specific global gene expression in humans.Probabilistic method for detecting copy number variation in a fetal genome using maternal plasma sequencing.Noninvasive prenatal diagnosis in a fetus at risk for methylmalonic acidemia.TroX: a new method to learn about the genesis of aneuploidy from trisomic products of conception.Assessment of circulating copy number variant detection for cancer screening.Towards standardisation of cell-free DNA measurement in plasma: controls for extraction efficiency, fragment size bias and quantification Recent advances in the prenatal interrogation of the human fetal genome.The future is now: single-cell genomics of bacteria and archaea Revised American Thyroid Association guidelines for the management of medullary thyroid carcinoma.Depletion of Abundant Sequences by Hybridization (DASH): using Cas9 to remove unwanted high-abundance species in sequencing libraries and molecular counting applications.Promises, pitfalls and practicalities of prenatal whole exome sequencing.DNA/RNA Detection Using DNA-Templated Few-Atom Silver Nanoclusters.Noninvasive prenatal molecular karyotyping from maternal plasma.Long-term persistence and effects of fetal microchimerisms on disease onset and status in a cohort of women with rheumatoid arthritis and systemic lupus erythematosus.Noninvasive prenatal testing for autosomal recessive conditions by maternal plasma sequencing in a case of congenital deafness.Developmental stage determines efficiency of gene transfer to muscle satellite cells by in utero delivery of adeno-associated virus vector serotype 2/9 Genetic counselors and Genomic Counseling in the United Kingdom.Haplotype-resolved whole-genome sequencing by contiguity-preserving transposition and combinatorial indexing.Analysis of cell-free DNA in maternal blood in screening for fetal aneuploidies: updated meta-analysis.Exome Sequencing in Fetuses with Structural Malformations Advancing the speed, sensitivity and accuracy of biomolecular detection using multi-length-scale engineering.Old Questions, New Paradigms: Ethical, Legal, and Social Complications of Noninvasive Prenatal Testing.From genes to genomes in the clinic.Evaluation of an Improved Non-invasive Fetal Sex Determination in Haemophilia A Patients Proof-of-principle rapid noninvasive prenatal diagnosis of autosomal recessive founder mutations Statistical Approach to Decreasing the Error Rate of Noninvasive Prenatal Aneuploid Detection caused by Maternal Copy Number Variation Applying deep DNA sequencing to common, complex pediatric traits.High-throughput sequencing and rare genetic diseases.The scope of prenatal diagnosis for women at increased risk for aneuploidies: views and preferences of professionals and potential users.Chromosomal microarray versus karyotyping for prenatal diagnosis.

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P2860

Non-invasive prenatal measurement of the fetal genome

http://www.wikidata.org/entity/Q34286073

description

2012 nî lūn-bûn

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2012 թուականի Յուլիսին հրատարակուած գիտական յօդուած

@hyw

2012 թվականի հուլիսին հրատարակված գիտական հոդված

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2012年の論文

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2012年論文

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2012年論文

@zh-hant

2012年論文

@zh-hk

2012年論文

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2012年論文

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2012年论文

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name

Non-invasive prenatal measurement of the fetal genome

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Non-invasive prenatal measurement of the fetal genome

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Non-invasive prenatal measurement of the fetal genome

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type

label

Non-invasive prenatal measurement of the fetal genome

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Non-invasive prenatal measurement of the fetal genome

@en

Non-invasive prenatal measurement of the fetal genome

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prefLabel

Non-invasive prenatal measurement of the fetal genome

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Non-invasive prenatal measurement of the fetal genome

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Non-invasive prenatal measurement of the fetal genome

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H Christina Fan

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Jianbin Wang

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Stephen R Quake

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Wei Gu

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Yair J Blumenfeld

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Yasser Y El-Sayed

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P2860

A map of human genome variation from population-scale sequencing

Noninvasive diagnosis of fetal aneuploidy by shotgun sequencing DNA from maternal blood

Measuring paternal discrepancy and its public health consequences

DNA sequencing of maternal plasma reliably identifies trisomy 18 and trisomy 13 as well as Down syndrome: an international collaborative study.

Detection and quantification of rare mutations with massively parallel sequencing.

Digital PCR provides sensitive and absolute calibration for high throughput sequencing.

Whole-genome molecular haplotyping of single cells

Performance comparison of exome DNA sequencing technologies.

DNA sequencing of maternal plasma to detect Down syndrome: an international clinical validation study.

Genomics and perinatal care

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