zCall: a rare variant caller for array-based genotyping: Genetics and population analysis
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Patrick F. Sullivan | Menachem Fromer | Benjamin M. Neale | Colm O'Dushlaine | George B. Grant | Steven A. McCarroll | Mark J. Daly | Christine Stevens | Christina M. Hultman | Pamela Sklar | Jason P. Carey | Andrew Crenshaw | Jennifer L. Moran | Jacqueline I. Goldstein | Jared Maguire | Kimberly Chambert | Shaun Purcell | J. Maguire | M. Daly | P. Sullivan | S. Mccarroll | B. Neale | S. Purcell | George B. Grant | P. Sklar | C. Hultman | K. Chambert | M. Fromer | A. Crenshaw | J. Goldstein | C. Stevens | J. Moran | Jason P. Carey | C. O’Dushlaine
[1] R Core Team,et al. R: A language and environment for statistical computing. , 2014 .
[2] James A. Morris,et al. optiCall: a robust genotype-calling algorithm for rare, low-frequency and common variants , 2012, Bioinform..
[3] R. Handsaker,et al. Genome-wide association study in a Swedish population yields support for greater CNV and MHC involvement in schizophrenia compared with bipolar disorder , 2012, Molecular Psychiatry.
[4] P. Visscher,et al. Five years of GWAS discovery. , 2012, American journal of human genetics.
[5] Joshua M. Korn,et al. Integrated genotype calling and association analysis of SNPs, common copy number polymorphisms and rare CNVs , 2008, Nature Genetics.
[6] D. Botstein,et al. Discovering genotypes underlying human phenotypes: past successes for mendelian disease, future approaches for complex disease , 2003, Nature Genetics.
[7] Ruijie Liu,et al. Comparing genotyping algorithms for Illumina's Infinium whole-genome SNP BeadChips , 2011, BMC Bioinformatics.