171
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BMCBI
2011
14 years 8 months ago
2011
Background: Copy number variants (CNVs), including deletions, amplifications, and other rearrangements, are common in human and cancer genomes. Copy number data from array compara...
174
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BMCBI
2011
14 years 8 months ago
2011
Background: Next generation ultra-sequencing technologies are starting to produce extensive quantities of data from entire human genome or exome sequences, and therefore new softw...
162
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BMCBI
2011
14 years 8 months ago
2011
Background: Identification of discourse relations, such as causal and contrastive relations, between situations mentioned in text is an important task for biomedical text-mining. ...
160
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BMCBI
2011
14 years 8 months ago
2011
Background: The implementation of high throughput sequencing for exploring biodiversity poses high demands on bioinformatics applications for automated data processing. Here we in...
154
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BMCBI
2011
14 years 8 months ago
2011
Background: The cost efficient two-stage design is often used in genome-wide association studies (GWASs) in searching for genetic loci underlying the susceptibility for complex di...
169
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BMCBI
2011
14 years 8 months ago
2011
Background: The search for cluster structure in microarray datasets is a base problem for the so-called “-omic sciences”. A difficult problem in clustering is how to handle da...
285
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BMCBI
2011
14 years 8 months ago
2011
Background: Discovering the genetic basis of common genetic diseases in the human genome represents a public health issue. However, the dimensionality of the genetic data (up to 1...
161
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BMCBI
2011
14 years 8 months ago
2011
Background: Next-generation sequencing (NGS) offers a unique opportunity for high-throughput genomics and has potential to replace Sanger sequencing in many fields, including de-n...
166
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BIOINFORMATICS
2011
14 years 8 months ago
2011
196
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BIOINFORMATICS
2011
14 years 8 months ago
2011