Rare Structural Variants
Author:
Publisher
Springer New York
Link
http://link.springer.com/content/pdf/10.1007/978-1-4939-2824-8_4
Reference63 articles.
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3. Amarasinghe KC, Li J, Halgamuge SK (2013) CoNVEX: copy number variation estimation in exome sequencing data using HMM. BMC Bioinformatics 14(Suppl 2):S2. doi: 10.1186/1471-2105-14-S2-S2
4. Aten E, White SJ, Kalf ME, Vossen RHAM, Thygesen HH, Ruivenkamp CA, Kriek M, Breuning MHB, den Dunnen JT (2008) Methods to detect CNVs in the human genome. Cytogenet Genome Res 123(1-4):313–321. doi: 10.1159/000184723
5. Bellos E, Johnson MR, Coin LJ (2012) CnvHiTSeq: integrative models for high-resolution copy number variation detection and genotyping using population sequencing data. Genome Biol 13(12):R120. doi: 10.1186/gb-2012-13-12-r120
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