Vineith Kaul

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PURPOSE Copy number variants have emerged as a major cause of human disease such as autism and intellectual disabilities. Because copy number variants are common in normal individuals, determining the functional and clinical significance of rare copy number variants in patients remains challenging. The adoption of whole-genome chromosomal microarray(More)
Saturated patterns with don't care like those emerged in biosequence motif discovery have proven a valuable notion also in the design of lossless and lossy compression of sequence data. In independent endeavors, the peculiarities inherent to the compression of tables have been examined, leading to compression schemata advantageously hinged on a prudent(More)
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