Amplification-free sequencing of cell-free DNA for prenatal non-invasive diagnosis of chromosomal aberrations-Reference-Cited by-同舟云学术

Amplification-free sequencing of cell-free DNA for prenatal non-invasive diagnosis of chromosomal aberrations

Published:2015-03 Issue:3 Volume:105 Page:150-158
ISSN:0888-7543
Container-title:Genomics
language:en
Short-container-title:Genomics

Author:

Karlsson Kasper,Sahlin Ellika,Iwarsson Erik,Westgren Magnus,Nordenskjöld Magnus,Linnarsson Sten

Funder

European Research Council

Swedish Research Council (STARGET)

Breast Cancer Theme Center

KI AstraZeneca Research Collaboration

Publisher

Elsevier BV

Subject

Genetics

Reference18 articles.

1. Recent advances in the prenatal interrogation of the human fetal genome;Hui;Trends Genet.,2012

2. Cell-free fetal DNA testing for fetal aneuploidy and beyond: clinical integration challenges in the US context;Allyse;Hum. Reprod.,2012

3. Non-invasive prenatal diagnosis of single-gene disorders from maternal blood;Bustamante-Aragones;Gene,2012

4. Fetal fraction in maternal plasma cell-free DNA at 11–13 weeks' gestation: relation to maternal and fetal characteristics;Ashoor;Ultrasound Obstet. Gynecol.,2012

5. Length and GC-biases during sequencing library amplification: a comparison of various polymerase-buffer systems with ancient and modern DNA sequencing libraries;Dabney;Biotechniques,2012

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