Results 231 to 240 of about 1,566,477 (261)

Design of a Bovine Low-Density SNP Array Optimized for Imputation

, 2012
Didier Boichard, Ho Young Chung, Romain Dassonneville, Xavier David, Andre A. Eggen, Sébastien Fritz, Kimberly Gietzen, Ben J. Hayes, Cindy Lawley, Tad S. Sonstegard, Curtis P. Van Tassell, P.M. VanRaden, Karine A. Viaud-Martinez, G.R. Wiggans   +13 more
openalex   +2 more sources

GCViT: a method for interactive, genome-wide visualization of resequencing and SNP array data. [PDF]

BMC Genomics, 2020
Wilkey AP, Brown AV, Cannon SB, Cannon EKS.   +3 more
europepmc   +1 more source

Identification of Genome-Wide Copy Number Variations among Diverse Pig Breeds Using SNP Genotyping Arrays

, 2013
Jiying Wang, Haifei Wang, Jicai Jiang, Huimin Kang, Xiaotian Feng, Qin Zhang, Jianfeng Liu   +6 more
openalex   +2 more sources

A SNP-Based Genetic Linkage Map of Soybean Using the SoyS - NP6K Illumina Infinium BeadChip Genotyping Array

, 2013
Masum Akond, Shiming Liu, Lauren Schoener, James A. Anderson, Stella K. Kantartzi, Khalid Meksem, Qijian Song, Dechun Wang, Zixiang Wen, David A. Lightfoot, My Abdelmajid Kassem   +10 more
openalex   +1 more source

Meta-analysis of exome array data identifies six novel genetic loci for lung function [version 3; referees: 2 approved] [PDF]

, 2018
et al,, Kraja, Aldi, Province, Michael A
core   +1 more source

Genome-Wide Copy Number Variations Inferred from SNP Genotyping Arrays Using a Large White and Minzhu Intercross Population

, 2013
Ligang Wang, Xin Liu, Longchao Zhang, Hua Yan, Weizhen Luo, Jing Liang, Duxue Cheng, Shaokang Chen, Xiaojun Ma, Xin Song, Kebin Zhao, Lixian Wang   +11 more
openalex   +2 more sources

Correction: SNP Array Analysis Reveals Novel Genomic Abnormalities Including Copy Neutral Loss of Heterozygosity in Anaplastic Oligodendrogliomas

, 2013
Ahmed Idbaïh, François Ducray, Caroline Dehais, Célia Courdy, Alain Carpentier, Simon Bernard, Emmanuelle Uro‐Coste, Karima Mokhtari, Anne Jouvet, Jérôme Honnorat, Olivier Chinot, Carole Ramirez, Patrick Beauchesne, Alexandra Benouaich‐Amiel, J Godard, Sandrine Eimer, Fabrice Parker, Emmanuèle Lechapt, Philippe Colin, Delphine Loussouarn, Thierry Faillot, Phong Dam‐Hieu, Selma Elouadhani-Hamdi, Luc Bauchet, Olivier Langlois, C. Le Guérinel, Denys Fontaine, Élodie Vauléon, Philippe Meneï, Marie Janette Motsuo Fotso, C. Desenclos, Pierre Verrelle, François Ghiringhelli, G. Noël, François Labrousse, Alain Carpentier, F. Dhermain, Jean‐Yves Delattre, Dominique Figarella‐Branger   +38 more
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Molecular Karyotyping: From Microscope to SNP Arrays

Hormone Research in Paediatrics, 2011
Chromosomal rearrangements are an important cause of distinctive and recognizable clinical phenotypes. For many years conventional karyotyping has been a successful tool to detect such chromosomal rearrangements. However, this technique has a limited resolution of 5–10 Mb.
Gijsbers, A.C.J., Ruivenkamp, C.A.L.
openaire   +4 more sources