A citation-based method for searching scientific literature

Laura Winchester, Christopher Yau, Jiannis Ragoussis. Brief Funct Genomic Proteomic 2009
Times Cited: 137



Roger Pique-Regi, Jordi Monso-Varona, Antonio Ortega, Robert C Seeger, Timothy J Triche, Shahab Asgharzadeh. Bioinformatics 2008
Times Cited: 87




List of shared articles



Times cited

DeepCNV: a deep learning approach for authenticating copy number variations.
Joseph T Glessner, Xiurui Hou, Cheng Zhong, Jie Zhang, Munir Khan, Fabian Brand, Peter Krawitz, Patrick M A Sleiman, Hakon Hakonarson, Zhi Wei. Brief Bioinform 2021
0

Genome-wide detection of copy number variations in polled yak using the Illumina BovineHD BeadChip.
Congjun Jia, Hongbo Wang, Chen Li, Xiaoyun Wu, Linsen Zan, Xuezhi Ding, Xian Guo, Pengjia Bao, Jie Pei, Min Chu,[...]. BMC Genomics 2019
5


A decade of structural variants: description, history and methods to detect structural variation.
Geòrgia Escaramís, Elisa Docampo, Raquel Rabionet. Brief Funct Genomics 2015
45


The Growing Importance of CNVs: New Insights for Detection and Clinical Interpretation.
Armand Valsesia, Aurélien Macé, Sébastien Jacquemont, Jacques S Beckmann, Zoltán Kutalik. Front Genet 2013
36

Genome-wide copy number variations inferred from SNP genotyping arrays using a Large White and Minzhu intercross population.
Ligang Wang, Xin Liu, Longchao Zhang, Hua Yan, Weizhen Luo, Jing Liang, Duxue Cheng, Shaokang Chen, Xiaojun Ma, Xin Song,[...]. PLoS One 2013
14

Comparative Analysis of CNV Calling Algorithms: Literature Survey and a Case Study Using Bovine High-Density SNP Data.
Lingyang Xu, Yali Hou, Derek M Bickhart, Jiuzhou Song, George E Liu. Microarrays (Basel) 2013
25


Algorithm implementation for CNV discovery using Affymetrix and Illumina SNP array data.
Laura Winchester, Jiannis Ragoussis. Methods Mol Biol 2012
1