Combining count- and length-based z-scores leads to improved predictions in non-invasive prenatal testing-Reference-Cited by-同舟云学术

Combining count- and length-based z-scores leads to improved predictions in non-invasive prenatal testing

Published:2018-09-14 Issue:8 Volume:35 Page:1284-1291
ISSN:1367-4803
Container-title:Bioinformatics
language:en
Short-container-title:

Author:

Budis Jaroslav¹²³^ORCID,Gazdarica Juraj²⁴,Radvanszky Jan²⁵,Szucs Gabor⁶,Kucharik Marcel⁷,Strieskova Lucia²⁴,Gazdaricova Iveta⁴,Harsanyova Maria²⁴,Duris Frantisek²³^ORCID,Minarik Gabriel⁷,Sekelska Martina⁷,Nagy Balint⁸,Turna Jan³⁴⁹,Szemes Tomas²⁴⁹

Affiliation:

1. Department of Computer Science, Faculty of Mathematics, Physics and Informatics, Comenius University, Bratislava, Slovakia

2. Bratislava, Geneton s.r.o, Bratislava, Slovakia

3. Slovak Centre of Scientific and Technical Information, Bratislava, Slovakia

4. Department of Molecular Biology, Faculty of Natural Sciences, Comenius University, Bratislava, Slovakia

5. Institute of Clinical and Translational Research, Biomedical Research Center, Slovak Academy of Sciences, Bratislava, Slovakia

6. Department of Applied Mathematics and Statistics, Faculty of Mathematics, Physics and Informatics, Comenius University, Bratislava, Slovakia

7. Medirex a.s, Bratislava, Slovakia

8. Department of Human Genetics, University of Debrecen, Debrecen, Hungary

9. Comenius University Science Park, Bratislava, Slovakia

Funder

Research & Developmental Operational Programme

European Regional Development Fund

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/35/8/1284/28500636/bty806.pdf

Reference45 articles.

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3. Dna sequencing versus standard prenatal aneuploidy screening;Bianchi;N. Engl. J. Med,2014

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5. Cancer genome scanning in plasma: detection of tumor-associated copy number aberrations, single-nucleotide variants, and tumoral heterogeneity by massively parallel sequencing;Chan;Clin. Chem,2012

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