Hui Wang

发表

Markov Models for Inferring Copy Number Variations from Genotype Data on Illumina Platforms

C. Sabatti, R. Ophoff, H. Blauw, 2009, Human Heredity.

Backward Genotype-Trait Association (BGTA)-Based Dissection of Complex Traits in Case-Control Designs

Tian Zheng, Shaw-Hwa Lo, S. Lo, 2006, Human Heredity.

Inferring genomic loss and location of tumor suppressor genes from high density genotypes

C. Sabatti, S. Nelson, Yohan Lee, 2005 .

Linkage Disequilibrium and Haplotype Homozygosity in Population Samples Genotyped at a High Marker Density

C. Sabatti, N. Freimer, Yuguo Chen, 2006, Human Heredity.

A genome-wide linkage scan of familial benign recurrent vertigo: linkage to 22q12 with evidence of heterogeneity.

C. Sabatti, S. Nelson, R. Baloh, 2006, Human molecular genetics.

A novel mutation in KCNA1 causes episodic ataxia without myokymia

C. Sabatti, S. Nelson, J. Jen, 2004, Human mutation.

Title Markov models for inferring Copy Number Variations from genotype data on Illumina platforms Permalink

C. Sabatti, J. Veldink, Hui Wang, 2008 .

Title Markov models for inferring Copy Number Variations from genotype data Permalink

C. Sabatti, J. Veldink, Hui Wang, 2008 .

Inferring genomic loss and location of tumor suppressor genes from high density genotypes

C. Sabatti, S. Nelson, Yohan Lee, 2005 .