(Q34374066)

1 August 2017

title

The feasibility study of non-invasive fetal trisomy 18 and 21 detection with semiconductor sequencing platform (English)

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1 August 2017

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17

Jong Bhak

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1 August 2017

Young Joo Jeon

1

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1 August 2017

Yulin Zhou

2

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1 August 2017

Yihan Li

3

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1 August 2017

Qiwei Guo

4

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1 August 2017

Jinchun Chen

5

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1 August 2017

Shengmao Quan

6

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1 August 2017

Ahong Zhang

7

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1 August 2017

Hailing Zheng

8

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1 August 2017

Xingqiang Zhu

9

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1 August 2017

Jin Lin

10

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1 August 2017

Huan Xu

11

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1 August 2017

Ayang Wu

12

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1 August 2017

Sin-Gi Park

13

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1 August 2017

Byung Chul Kim

14

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1 August 2017

Hee Jae Joo

15

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1 August 2017

Hongliang Chen

16

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1 August 2017

language of work or name

English

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publication date

20 October 2014

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1 August 2017

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1 August 2017

volume

9

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1 August 2017

issue

10

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1 August 2017

page(s)

e110240

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Creative Commons Attribution 4.0 International

1 August 2017

copyright license

start time

20 October 2014

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April 2022 Public Data File from Crossref

copyright status

copyrighted

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cites work

Noninvasive prenatal diagnosis of common aneuploidies by semiconductor sequencing

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4203771

Performance comparison between rapid sequencing platforms for ultra-low coverage sequencing strategy

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4203771

DNA Sequencing versus Standard Prenatal Aneuploidy Screening

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4203771

Fetoplacental mosaicism: potential implications for false-positive and false-negative noninvasive prenatal screening results.

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4203771

Non-invasive prenatal testing for fetal chromosomal abnormalities by low-coverage whole-genome sequencing of maternal plasma DNA: review of 1982 consecutive cases in a single center

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4203771

Maternal mosaicism is a significant contributor to discordant sex chromosomal aneuploidies associated with noninvasive prenatal testing

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4203771

Non-invasive prenatal testing for aneuploidy: current status and future prospects

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4203771

The new sequencer on the block: comparison of Life Technology's Proton sequencer to an Illumina HiSeq for whole-exome sequencing

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4203771

Clinical utility and cost of non-invasive prenatal testing with cfDNA analysis in high-risk women based on a US population

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4203771

A tale of three next generation sequencing platforms: comparison of Ion Torrent, Pacific Biosciences and Illumina MiSeq sequencers

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4203771

Noninvasive prenatal detection and selective analysis of cell-free DNA obtained from maternal blood: evaluation for trisomy 21 and trisomy 18.

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4203771

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

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4203771

Screening for fetal aneuploidies at 11 to 13 weeks

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4203771

Update on Procedure-Related Risks for Prenatal Diagnosis Techniques

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4203771

SOAP2: an improved ultrafast tool for short read alignment

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4203771

Fast and accurate short read alignment with Burrows-Wheeler transform

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4203771

Ultrafast and memory-efficient alignment of short DNA sequences to the human genome

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4203771

ACOG Practice Bulletin No. 77: Screening for Fetal Chromosomal Abnormalities

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4203771

First-trimester screening for trisomy 21 combining biochemistry and ultrasound at individually optimal gestational ages. An interventional study

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4203771

Rapid clearance of fetal DNA from maternal plasma

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4203771

Impact of introducing a national policy for prenatal Down syndrome screening on the diagnostic invasive procedure rate in England.

6 July 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0110240

Analysis of the impact of PAPP-A, free β-hCG and nuchal translucency thickness on the advanced first trimester screening.

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0110240

First trimester contingent test as a screening method for Down's syndrome. A prospective study in the general population

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0110240

Non-Invasive Chromosomal Evaluation (NICE) Study: results of a multicenter prospective cohort study for detection of fetal trisomy 21 and trisomy 18.

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0110240

Size distributions of maternal and fetal DNA in maternal plasma.

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0110240

Screening advances and diagnostic choice: the problem of residual risk

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0110240

Presence of fetal DNA in maternal plasma and serum

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0110240

Screening for trisomy 21 by maternal age, fetal nuchal translucency thickness, free beta-human chorionic gonadotropin and pregnancy-associated plasma protein-A

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0110240

No evidence of fetal DNA persistence in maternal plasma after pregnancy

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4203771

Contingent screening for Down syndrome completed in the first trimester: a multicenter study

27 October 2018

1 reference

12 December 2020

Maternal source of false-positive fetal sex chromosome aneuploidy in noninvasive prenatal testing

1 reference

12 December 2020

Risk assessment of amniocentesis between 11 and 15 weeks: comparison to later amniocentesis controls

1 reference

12 December 2020

Chorionic villus sampling by biopsy forceps. Results of 1580 procedures from a single centre

1 reference

12 December 2020

Accepting or declining the offer of prenatal screening for congenital defects: test uptake and women's reasons

1 reference

12 December 2020

Noninvasive detection of fetal trisomy 21 by sequencing of DNA in maternal blood: a study in a clinical setting

1 reference

12 December 2020

Chromosome-selective sequencing of maternal plasma cell–free DNA for first-trimester detection of trisomy 21 and trisomy 18

1 reference

12 December 2020

10.1371/JOURNAL.PONE.0110240

Identifiers

DOI

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1 August 2017

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1 August 2017

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