PublisherDOIYearVolumeIssuePageTitleAuthor(s)Link
Genomics & Informatics10.5808/gi.2012.10.3.1942012103194Effect of Combining Multiple CNV Defining Algorithms on the Reliability of CNV Calls from SNP Genotyping DataSoon-Young Kim, Ji-Hong Kim, Yeun-Jun Chunghttp://synapse.koreamed.org/DOIx.php?id=10.5808/GI.2012.10.3.194
Cytogenetic and Genome Research10.1159/00018472220081231-4307-312CNV discovery using SNP genotyping arraysC. Yau, C.C. Holmeshttps://www.karger.com/Article/Pdf/184722, https://www.karger.com/Article/Pdf/184722
Microarrays10.3390/microarrays2030171201323171-185Comparative Analysis of CNV Calling Algorithms: Literature Survey and a Case Study Using Bovine High-Density SNP DataLingyang Xu, Yali Hou, Derek Bickhart, Jiuzhou Song, George Liuhttp://www.mdpi.com/2076-3905/2/3/171/pdf
Human Mutation10.1002/humu.222882013345763-773An MLPA-Based Strategy for Discrete CNV Genotyping: CNV-miRNAs as an ExampleMalgorzata Marcinkowska-Swojak, Barbara Uszczynska, Marek Figlerowicz, Piotr Kozlowskihttps://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1002%2Fhumu.22288, https://onlinelibrary.wiley.com/doi/full/10.1002/humu.22288
Cancer Informatics10.4137/cin.s16345201413s7CIN.S16345Hidden Markov Model-Based CNV Detection Algorithms for Illumina Genotyping MicroarraysEric L. Seiser, Federico Innocentihttp://journals.sagepub.com/doi/pdf/10.4137/CIN.S16345, http://journals.sagepub.com/doi/full-xml/10.4137/CIN.S16345, http://journals.sagepub.com/doi/pdf/10.4137/CIN.S16345
Journal of Animal Science10.1093/jas/skac247.3762022100Supplement_3207-207PSXII-1 CNV and Cnvr Detection from High-Density SNP Genotyping in Holstein CattleGiovanni C Ladeira, Pablo J Pinedo, Jose E P Santos, William W Thatcher, Fernanda M Rezendehttps://academic.oup.com/jas/article-pdf/100/Supplement_3/207/45963356/skac247.376.pdf, https://academic.oup.com/jas/article-pdf/100/Supplement_3/207/45963356/skac247.376.pdf
European Neuropsychopharmacology10.1016/j.euroneuro.2018.07.006201929S1022A COMPARATIVE ANALYSIS OF CNV RISK ACROSS MULTIPLE PSYCHIATRIC DISORDERSOmar Shanta, PGC CNVhttps://api.elsevier.com/content/article/PII:S0924977X18301779?httpAccept=text/xml, https://api.elsevier.com/content/article/PII:S0924977X18301779?httpAccept=text/plain
New Biotechnology10.1016/j.nbt.2010.01.022201027S25Stochastic CGH methods for CNV and SNP analysesG.V. Popescuhttps://api.elsevier.com/content/article/PII:S1871678410000245?httpAccept=text/xml, https://api.elsevier.com/content/article/PII:S1871678410000245?httpAccept=text/plain
Genetics Selection Evolution10.1186/1297-9686-42-342010421Reconstructing CNV genotypes using segregation analysis: combining pedigree information with CNV assayJohn M Henshall, Vicki A Whan, Belinda J Norrishttp://link.springer.com/content/pdf/10.1186/1297-9686-42-34.pdf, http://link.springer.com/article/10.1186/1297-9686-42-34/fulltext.html, http://link.springer.com/content/pdf/10.1186/1297-9686-42-34.pdf
Genetic Epidemiology10.1002/gepi.216432012365488-498Inheritance Model Introduces Differential Bias in CNV Calls Between Parents and OffspringSulgi Kim, Steven P. Millard, Chang-En Yu, Lesley Leong, Allen Radant, Dorcas Dobie, Debby W. Tsuang, Ellen M. Wijsmanhttps://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1002%2Fgepi.21643, http://onlinelibrary.wiley.com/wol1/doi/10.1002/gepi.21643/fullpdf