AMYCNE: Confident copy number assessment using whole genome sequencing data-Reference-Cited by-同舟云学术

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AMYCNE: Confident copy number assessment using whole genome sequencing data

Published:2018-03-26 Issue:3 Volume:13 Page:e0189710
ISSN:1932-6203
Container-title:PLOS ONE
language:en
Short-container-title:PLoS ONE

Author:

Eisfeldt Jesper^ORCID,Nilsson Daniel,Andersson-Assarsson Johanna C.,Lindstrand Anna

Funder

Vetenskapsrådet

Marianne and Marcus Wallenberg foundation

Svenska Sällskapet för Medicinsk Forskning

Kommunfullmäktige, Stockholms Stad

Harald and Greta Jeanssons Foundation

Ulf Lundahl Memory Fund through the Swedish Brain Foundation

Nilsson Ehle donations

IngaBritt och Arne Lundbergs Forskningsstiftelse

Erik Rönnberg Foundation

Publisher

Public Library of Science (PLoS)

Subject

Multidisciplinary

Reference21 articles.

1. A copy number variation map of the human genome;M Zarrei;Nat Rev Genet,2015

2. Copy number variants and genetic traits: closer to the resolution of phenotypic to genotypic variability;JS Beckmann;Nat Rev Genet,2007

3. Global variation in copy number in the human genome;R Ishikawa Redon;Nature,2006

4. Diet and the evolution of human amylase gene copy number variation;GH Perry;Nat Genet,2007

5. Low Copy Number of the AMY1 Locus Is Associated with Early-Onset Female Obesity in Finland;H Viljakainen;PLoS One,2015

Cited by 22 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Genetic variation and molecular profiling of congenital malformations of the female genital tract based on whole-genome sequencing;World Journal of Pediatrics;2024-09-09

2. Case report: Second report of neuromuscular syndrome caused by biallelic variants in ASCC3;Frontiers in Genetics;2024-09-02

3. High-coverage genome sequencing of Yayoi and Jomon individuals shed light on prehistoric human population history in East Eurasian;2024-08-12

4. GeneToCN: an alignment-free method for gene copy number estimation directly from next-generation sequencing reads;Scientific Reports;2023-10-18

5. Whole genome sequencing vs chromosomal microarray analysis in prenatal diagnosis;American Journal of Obstetrics and Gynecology;2023-09

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