Revisiting Mendelian disorders through exome sequencing

由 Ku, C.-S., Naidoo, N., Pawitan, Y.
出版 2014

The pursuit of genome-wide association studies: Where are we now

由 Ku, C.S., Loy, E.Y., Chia, K.S., Pawitan, Y.
出版 2011

Modified least-variant set normalization for miRNA microarray

由 Suo, C., Salim, A., Chia, K.-S., Pawitan, Y., Calza, S.
出版 2014

Regions of homozygosity and their impact on complex diseases and traits

由 Ku, C.S., Naidoo, N., Teo, S.M., Pawitan, Y.
出版 2014

How many genetic variants remain to be discovered?

由 Pawitan, Y., Seng, K.C., Magnusson, P.K.E.
出版 2014

The pursuit of genome-wide association studies: Where are we now

由 Ku, C.S., Loy, E.Y., Chia, K.S., Pawitan, Y.
出版 2011

Identification of recurrent regions of copy-number variants across multiple individuals

由 Mei, T.S., Salim, A., Seng, C.K., Calza, S., Pawitan, Y.
出版 2011

Finding regions of significance in SELDI measurements for identifying protein biomarkers

由 Tan, C.S., Ploner, A., Quandt, A., Pawitan, Y., Lehtio, J.
出版 2011

The discovery of human genetic variations and their use as disease markers: Past, present and future

由 Ku, C.S., Loy, E.Y., Salim, A., Pawitan, Y., Chia, K.S.
出版 2014

Statistical challenges associated with detecting copy number variations with next-generation sequencing

由 Teo, S.M., Pawitan, Y., Ku, C.S., Chia, K.S., Salim, A.
出版 2014

Classification of array CGH data using smoothed logistic regression model

由 Huang, J., O'Sullivan, K., Salim, A., Lei, K., Pawitan, Y.
出版 2011

Human genetics and genomics a decade after the release of the draft sequence of the human genome

由 Naidoo, N., Pawitan, Y., Soong, R., Cooper, D.N., Ku, C.-S.
出版 2014

Regions of homozygosity in three Southeast Asian populations

由 Teo, S.-M., Ku, C.-S., Salim, A., Naidoo, N., Chia, K.-S., Pawitan, Y.
出版 2014

Correlating gene and protein expression data using correlated factor analysis

由 Tan, C.S., Ploner, A., Chia, K.S., Pawitan, Y., Salim, A., Lehtio, J.
出版 2011

Annotated regions of significance of SELDI-TOF-MS spectra for detecting protein biomarkers

由 Tan, C.S., Ploner, A., Quandt, A., Pawitan, Y., Lehtio, J., Pernemalm, M., Lewensohn, R.
出版 2011

A population-based study of copy number variants and regions of homozygosity in healthy Swedish individuals

由 Teo, S.-M., Ku, C.-S., Naidoo, N., Hall, P., Chia, K.-S., Salim, A., Pawitan, Y.
出版 2014

Estimating the number of true discoveries in genome-wide association studies

由 Lee, W., Gusnanto, A., Salim, A., Magnusson, P., Sim, X., Tai, E.S., Pawitan, Y.
出版 2014

Multi-platform segmentation for joint detection of copy number variants

由 Teo, S.M., Pawitan, Y., Kumar, V., Thalamuthu, A., Seielstad, M., Chia, K.S., Salim, A.
出版 2014

Gene discovery in familial cancer syndromes by exome sequencing: Prospects for the elucidation of familial colorectal cancer type X

由 Ku, C.-S., Cooper, D.N., Wu, M., Roukos, D.H., Pawitan, Y., Soong, R., Iacopetta, B.
出版 2014

Technological advances in DNA sequence enrichment and sequencing for germline genetic diagnosis

由 Ku, C.-S., Wu, M., Cooper, D.N., Naidoo, N., Pawitan, Y., Pang, B., Iacopetta, B., Soong, R.
出版 2014