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Works
10
Dissecting the genetic basis of comorbid epilepsy phenotypes in neurodevelopmental disorders
The discovery of integrated gene networks for autism and related disorders
Resolving the complexity of the human genome using single-molecule sequencing
Neurodevelopmental disease genes implicated by de novo mutation and copy number variation morbidity
Discovery of tandem and interspersed segmental duplications using high throughput sequencing
Combinatorial algorithms for structural variation detection in high-throughput sequenced genomes
Discovery of tandem and interspersed segmental duplications using high-throughput sequencing
mrsFAST: a cache-oblivious algorithm for short-read mapping.
Combinatorial Approach for Complex Disorder Prediction: Case Study of Neurodevelopmental Disorders
Mapping copy number variation by population-scale genome sequencing
