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Using ERDS to Infer Copy-Number Variants in High-Coverage GenomesMINGFU ZHU; NEED, Anna C; RUZZO, Elizabeth K et al.American journal of human genetics. 2012, Vol 91, Num 3, pp 408-421, issn 0002-9297, 14 p.Article

Multi-platform segmentation for joint detection of copy number variantsSHU MEI TEO; PAWITAN, Yudi; KUMAR, Vikrant et al.Bioinformatics (Oxford. Print). 2011, Vol 27, Num 11, pp 1555-1561, issn 1367-4803, 7 p.Article

VEGA: variational segmentation for copy number detectionMORGANELLA, Sandro; CERULO, Luigi; VIGLIETTO, Giuseppe et al.Bioinformatics (Oxford. Print). 2010, Vol 26, Num 24, pp 3020-3027, issn 1367-4803, 8 p.Article

Personalized copy number and segmental duplication maps using next-generation sequencingATKAN, Can; KIDD, Jeffrey M; SAHINALP, S. Cenk et al.Nature genetics. 2009, Vol 41, Num 10, pp 1061-1067, issn 1061-4036, 7 p.Article

CNVDetector : locating copy number variations using array CGH dataGHEN, Peng-An; LIU, Hsiao-Fei; GHAO, Kun-Mao et al.Bioinformatics (Oxford. Print). 2008, Vol 24, Num 23, pp 2773-2775, issn 1367-4803, 3 p.Article

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Copy-number polymorphisms: mining the tip of an icebergBUCKLEY, Patrick G; MANTRIPRAGADA, Kiran K; PIOTROWSKI, Arkadiusz et al.Trends in genetics (Regular ed.). 2005, Vol 21, Num 6, pp 315-317, issn 0168-9525, 3 p.Article

Copy-Number Gains of HUWE1 Due to Replication- and Recombination-Based RearrangementsFROYEN, Guy; BELET, Stefanie; GONCALVES PIMENTEL, Marcia Mattos et al.American journal of human genetics. 2012, Vol 91, Num 2, pp 252-264, issn 0002-9297, 13 p.Article

Read count approach for DNA copy number variants detectionMAGI, Alberto; TATTINI, Lorenzo; PIPPUCCI, Tommaso et al.Bioinformatics (Oxford. Print). 2012, Vol 28, Num 4, pp 470-478, issn 1367-4803, 9 p.Article

Copy Number Variants: Mapping the Genome's 'Land Mines'PERKEL, Jeffrey M.BioTechniques. 2011, Vol 51, Num 1, pp 21-24, issn 0736-6205, 4 p.Article

A segmental maximum a posteriori approach to genome-wide copy number profilingANDERSSON, Robin; BRUDER, Carl E. G; PIOTROWSKI, Arkadiusz et al.Bioinformatics (Oxford. Print). 2008, Vol 24, Num 6, pp 751-758, issn 1367-4803, 8 p.Article

Analysis of genome-wide copy number variation in Irish and Dutch ALS populationsCRONIN, Simon; BLAUW, Hylke M; VELDINK, Jan H et al.Human molecular genetics (Print). 2008, Vol 17, Num 21, pp 3392-3398, issn 0964-6906, 7 p.Article

Extending genome-wide association studies to copy-number variationMCCARROLL, Steven A.Human molecular genetics (Print). 2008, Vol 17, issn 0964-6906, R135-R142, NS2Article

Cytogenetically balanced translocations are associated with focal copy number alterationsWATSON, Spencer K; DELEEUW, Ronald J; HORSMAN, Doug E et al.Human genetics. 2007, Vol 120, Num 6, pp 795-805, issn 0340-6717, 11 p.Article

Methods and strategies for analyzing copy number variation using DNA microarraysCARTER, Nigel P.Nature genetics. 2007, Vol 39, Num 7, issn 1061-4036, S16-S21, SUPArticle

A Comparison of DNA Copy Number Profiling PlatformsGRESHOCK, Joel; BIN FENG; NOGUEIRA, Cristina et al.Cancer research (Baltimore). 2007, Vol 67, Num 21, pp 10173-10180, issn 0008-5472, 8 p.Article

Twinkle helicase is essential for mtDNA maintenance and regulates mtDNA copy numberTYYNISMAA, Henna; SEMBONGI, Hiroshi; BOKORI-BROWN, Monika et al.Human molecular genetics (Print). 2004, Vol 13, Num 24, pp 3219-3227, issn 0964-6906, 9 p.Article

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False positive peaks in ChIP-seq and other sequencing-based functional assays caused by unannotated high copy number regionsPICKRELL, Joseph K; GAFFNEY, Daniel J; GILAD, Yoav et al.Bioinformatics (Oxford. Print). 2011, Vol 27, Num 15, pp 2144-2146, issn 1367-4803, 3 p.Article

Finding recurrent copy number alterations preserving within-sample homogeneityMORGANELLA, Sandro; PAGNOTTA, Stefano Maria; CECCARELLI, Michele et al.Bioinformatics (Oxford. Print). 2011, Vol 27, Num 21, pp 2949-2956, issn 1367-4803, 8 p.Article

FCGR3B copy number variation is associated with susceptibility to systemic, but not organ-specific, autoimmunityFANCIULLI, Manuela; NORSWORTHY, Penny J; FROGUEL, Philippe et al.Nature genetics. 2007, Vol 39, Num 6, pp 723-725, issn 1061-4036, 3 p.Article

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Parent-specific copy number in paired tumor-normal studies using circular binary segmentationOLSHEN, Adam B; BENGTSSON, Henrik; NEUVIAL, Pierre et al.Bioinformatics (Oxford. Print). 2011, Vol 27, Num 15, pp 2038-2046, issn 1367-4803, 9 p.Article