(Q36998320)

17 August 2017

Haplotype-assisted accurate non-invasive fetal whole genome recovery through maternal plasma sequencing (English)

1 reference

17 August 2017

whole genome sequencing

1 reference

Jun Wang

17

0 references

Yang Huanming

19

object named as

Huanming Yang

1 reference

17 August 2017

21

Xiuqing Zhang

1 reference

17 August 2017

15

Wei Wang

1 reference

17 August 2017

Shengpei Chen

1

1 reference

17 August 2017

Huijuan Ge

2

1 reference

17 August 2017

Xuebin Wang

3

1 reference

17 August 2017

Xiaoyu Pan

4

1 reference

17 August 2017

Xiaotian Yao

5

1 reference

17 August 2017

Xuchao Li

6

1 reference

17 August 2017

Chunlei Zhang

7

1 reference

17 August 2017

Fang Chen

8

1 reference

17 August 2017

Fuman Jiang

9

1 reference

17 August 2017

Peipei Li

10

1 reference

17 August 2017

Hui Jiang

11

1 reference

17 August 2017

Hancheng Zheng

12

1 reference

17 August 2017

Lei Zhang

13

1 reference

17 August 2017

Lijian Zhao

14

1 reference

17 August 2017

Songgang Li

16

1 reference

17 August 2017

Jian Wang

18

1 reference

17 August 2017

Yingrui Li

20

1 reference

17 August 2017

27 February 2013

1 reference

17 August 2017

1 reference

17 August 2017

5

1 reference

17 August 2017

2

1 reference

17 August 2017

18

1 reference

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

17 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3706925

Non-invasive prenatal measurement of the fetal genome

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3706925

Noninvasive whole-genome sequencing of a human fetus.

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3706925

Whole-genome molecular haplotyping of single cells

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3706925

Haplotype-resolved genome sequencing of a Gujarati Indian individual.

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3706925

Exome sequencing identifies the cause of a mendelian disorder

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3706925

Potential etiologic and functional implications of genome-wide association loci for human diseases and traits

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3706925

High-density genotyping of STAT4 reveals multiple haplotypic associations with systemic lupus erythematosus in different racial groups

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3706925

A unified approach to genotype imputation and haplotype-phase inference for large data sets of trios and unrelated individuals

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3706925

Noninvasive prenatal diagnosis of fetal chromosomal aneuploidy by massively parallel genomic sequencing of DNA in maternal plasma

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3706925

The diploid genome sequence of an Asian individual

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3706925

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

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3706925

Transgenerational epigenetic effects.

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3706925

Insertion-deletion polymorphisms (indels) as genetic markers in natural populations

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3706925

The diploid genome sequence of an individual human

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3706925

A SNP in the ABCC11 gene is the determinant of human earwax type

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3706925

Quantitative analysis of fetal DNA in maternal plasma and serum: implications for noninvasive prenatal diagnosis.

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3706925

PCR quantitation of fetal cells in maternal blood in normal and aneuploid pregnancies

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3706925

Randomised controlled trial of genetic amniocentesis in 4606 low-risk women

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3706925

Isolation of fetal DNA from nucleated erythrocytes in maternal blood

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3706925

Fetal cells in the blood of pregnant women: detection and enrichment by fluorescence-activated cell sorting

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3706925

Prenatal diagnosis of sickle cell anaemia and thalassaemia by analysis of fetal cells in maternal blood

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3706925

[Association between single-nucleotide polymorphisms in the IRAK-4 gene and allergic rhinitis].

27 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3706925

DNA sequencing of maternal plasma to identify Down syndrome and other trisomies in multiple gestations

4 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3706925

Life Technologies promises $1,000 genome.

4 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3706925

First-trimester or second-trimester screening, or both, for Down's syndrome

4 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3706925

A strong association between human earwax-type and apocrine colostrum secretion from the mammary gland

4 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3706925

Maternal Plasma DNA Sequencing Reveals the Genome-Wide Genetic and Mutational Profile of the Fetus

4 September 2018

1 reference

Crossref

https://api.crossref.org/works/10.1186%2FGM422

Noninvasive Prenatal Detection of Fetal Trisomy 18 by Epigenetic Allelic Ratio Analysis in Maternal Plasma: Theoretical and Empirical Considerations

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1186%2FGM422

Antenatal screening for Down's syndrome

21 January 2018

1 reference

12 December 2020

Prenatal screening and the reduction of birth defects in populations

1 reference

12 December 2020

First-trimester screening for trisomies 21 and 18

1 reference

12 December 2020

ACOG Practice Bulletin No. 88, December 2007. Invasive prenatal testing for aneuploidy

1 reference

12 December 2020

Identifiers

DOI

10.1186/GM422

1 reference

Dimensions Publication ID

17 August 2017

0 references

1 reference

17 August 2017

PubMed publication ID

23445748

1 reference