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J. T. Gene Hwang

dblp:96/5302 · DBLP profile ↗
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3ranked-venue papers
0as first author
0since 2021 · last 2008
—ORCID · none

Domains — the database's venue-derived domains; a paper can count in several

Applied, interdisciplinary, general and emerging computing · 3

Expertise — from the expertise taxonomy: the topics of the expert's papers under the CCF categories. A weight counts papers with recency: 1 for a paper about the topic, 0.3 when the topic is its context, halved every five years.

Interdisciplinary, comprehensive, and emerging computing
2 papers
Bioinformatics and computational biology · 100%

Topics — the 2 heaviest of 2, each with the papers that count most for it

TopicWeightPapersLastEvidence papers
Bioinformatics and computational biology › gene expression analysis
microarray data analysis
0.222008
Gene expression: Quick calculation for sample size while controlling false discovery rate with application to microarray analysis · Bioinform. 2008
Quick calculation for sample size while controlling false discovery rate with application to microarray analysis · Bioinform. 2007
Bioinformatics and computational biology › biostatistics
sample size determination
0.222008
Gene expression: Quick calculation for sample size while controlling false discovery rate with application to microarray analysis · Bioinform. 2008
Quick calculation for sample size while controlling false discovery rate with application to microarray analysis · Bioinform. 2007

Methods — techniques the papers use, named apart from their topics

t-test · 0.1q-value procedure · 0.1f-test · 0.1
YearPublicationVenuePosition
2008 Gene expression: Quick calculation for sample size while controlling false discovery rate with application to microarray analysis
Peng Liu 0007, J. T. Gene Hwang
Bioinform.2
2007 Quick calculation for sample size while controlling false discovery rate with application to microarray analysis
abstract
MOTIVATION: Sample size calculation is important in experimental design and is even more so in microarray or proteomic experiments since only a few repetitions can be afforded. In the multiple testing problems involving these experiments, it is more powerful and more reasonable to control false discovery rate (FDR) or positive FDR (pFDR) instead of type I error, e.g. family-wise error rate (FWER). When controlling FDR, the traditional approach of estimating sample size by controlling type I error is no longer applicable. RESULTS: Our proposed method applies to controlling FDR. The sample size calculation is straightforward and requires minimal computation, as illustrated with two sample t-tests and F-tests. Based on simulation with the resultant sample size, the power is shown to be achievable by the q-value procedure. AVAILABILITY: A Matlab code implementing the described methods is available upon request.
Peng Liu 0007, J. T. Gene Hwang
Bioinform.2
2002 Classification of pixels in a noisy grayscale image of polar ice
abstract
Often, in synthetic aperture radar (SAR) images of polar ice, one encounters shadow-like features across the images. Such features make it difficult to classify pixels into ice and water. Accordingly, it becomes a challenge to determine the true size and boundaries of ice floes in an SAR image of polar ice. We develop a simple statistical procedure which classifies pixels of an image by eliminating the effects of shadow-like features. Methodology developed in this paper is illustrated using some noisy SAR images of ice floes in the Arctic sea.
Shyamal D. Peddada, J. T. Gene Hwang
IEEE Trans. Geosci. Remote. Sens.2