iCall: a genotype-calling algorithm for rare, low-frequency and common variants on the Illumina exome array
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Yi Li | Jin Zhou | Jianjun Liu | Rick Twee-Hee Ong | Yik-Ying Teo | Erwin Tantoso | Lai-Ping Wong | Chiea-Chuen Khor | Jin-Xin Bei | Y. Teo | Jianjun Liu | C. Khor | Yi Li | R. Ong | E. Tantoso | J. Bei | Lai-Ping Wong | Jin Zhou
[1] Jing Huang,et al. Dynamic model based algorithms for screening and genotyping over 100K SNPs on oligonucleotide microarrays , 2005, Bioinform..
[2] Jean Yee Hwa Yang,et al. A multi-array multi-SNP genotyping algorithm for Affymetrix SNP microarrays , 2007, Bioinform..
[3] Michael Inouye,et al. A genotype calling algorithm for the Illumina BeadArray platform , 2007, Bioinform..
[4] Zhaohui S. Qin,et al. A second generation human haplotype map of over 3.1 million SNPs , 2007, Nature.
[5] Eleni Giannoulatou,et al. GenoSNP: a variational Bayes within-sample SNP genotyping algorithm that does not require a reference population , 2008, Bioinform..
[6] Zhaoxia Yu,et al. Genotype determination for polymorphisms in linkage disequilibrium , 2008, BMC Bioinformatics.
[7] Zhaoxia Yu,et al. Simultaneous genotype calling and haplotype phasing improves genotype accuracy and reduces false-positive associations for genome-wide association studies. , 2009, American journal of human genetics.
[8] Deanne M. Taylor,et al. Powerful SNP-set analysis for case-control genome-wide association studies. , 2010, American journal of human genetics.
[9] Kathryn Roeder,et al. Testing for an Unusual Distribution of Rare Variants , 2011, PLoS genetics.
[10] Xihong Lin,et al. Rare-variant association testing for sequencing data with the sequence kernel association test. , 2011, American journal of human genetics.
[11] Patrick F. Sullivan,et al. zCall: a rare variant caller for array-based genotyping: Genetics and population analysis , 2012, Bioinform..
[12] G. McVean,et al. Differential confounding of rare and common variants in spatially structured populations , 2011, Nature Genetics.
[13] James A. Morris,et al. optiCall: a robust genotype-calling algorithm for rare, low-frequency and common variants , 2012, Bioinform..
[14] Iuliana Ionita-Laza,et al. Sequence kernel association tests for the combined effect of rare and common variants. , 2013, American journal of human genetics.