Statistical model for whole genome sequencing and its application to minimally invasive diagnosis of fetal genetic disease-Reference-Cited by-同舟云学术

Statistical model for whole genome sequencing and its application to minimally invasive diagnosis of fetal genetic disease

Published:2009-03-23 Issue:10 Volume:25 Page:1244-1250
ISSN:1367-4803
Container-title:Bioinformatics
language:en
Short-container-title:Bioinformatics

Author:

Chu T.,Bunce K.,Hogge W. A.,Peters D. G.

Publisher

Oxford University Press (OUP)

Subject

Computational Mathematics,Computational Theory and Mathematics,Computer Science Applications,Molecular Biology,Biochemistry,Statistics and Probability

Link

http://academic.oup.com/bioinformatics/article-pdf/25/10/1244/755219/btp156.pdf

Reference14 articles.

1. A prospective analysis of cell-free fetal DNA concentration in maternal plasma as an indicator for adverse pregnancy outcome

2. Regionalized GC content of template DNA as a predictor of PCR success

3. Hypermethylated RASSF1A in Maternal Plasma: A Universal Fetal DNA Marker that Improves the Reliability of Noninvasive Prenatal Diagnosis

4. Mapping translocation breakpoints by next-generation sequencing

5. Systematic Search for Placental DNA-Methylation Markers on Chromosome 21: Toward a Maternal Plasma-Based Epigenetic Test for Fetal Trisomy 21

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2. Two approaches for calculating female fetal DNA fraction in noninvasive prenatal testing based on size analysis of maternal DNA fragments;BIOCELL;2022

3. Two approaches for calculating female fetal DNA fraction in noninvasive prenatal testing based on size analysis of maternal DNA fragments;BIOCELL;2022

4. Non‐invasive epigenomic molecular phenotyping of the human brain via liquid biopsy of cerebrospinal fluid and next generation sequencing;European Journal of Neuroscience;2020-10-22

5. An efficient method for noninvasive prenatal diagnosis of fetal trisomy 13, trisomy 18, and trisomy 21;PLOS ONE;2019-04-12