Rahul Roy Chowdhury

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This study was undertaken to decipher the interdependent roles of (i) methylation within E2 binding site I and II (E2BS-I/II) and replication origin (nt 7862) in the long control region (LCR), (ii) expression of viral oncogene E7, (iii) expression of the transcript (E7-E1/E4) that encodes E2 repressor protein and (iv) viral load, in human papillomavirus 16(More)
The major histocompatibility complex (MHC) is located on human Chromosome 6 and includes clusters of class I, class II, and class III genes. Centromeric to the class I region is a cluster of genes designated as MHC class IV encoding genes involved in immunity and inflammation, including the 1C7 gene. The human 1C7 gene has several alternatively spliced(More)
In recent times enumerable number of clustering algorithms have been developed whose main function is to make sets of objects having almost the same features. But due to the presence of categorical data values, these algorithms face a challenge in their implementation. Also some algorithms which are able to take care of categorical data are not able to(More)
Cars are an essential part of our everyday life. Nowadays we have a wide plethora of cars produced by a number of companies in all segments. The buyer has to consider a lot of factors while buying a car which makes the whole process a lot more difficult. So in this paper we have developed a method of ensemble learning to aid people in making the decision.(More)
The Homeobox (HOX) genes encode important transcription factors showing deregulated expression in several cancers. However, their role in cervical cancer pathogenesis, remains largely unexplored. Herein, we studied their association with Human Papillomavirus type 16 (HPV16) mediated cervical cancers. Our previously published gene expression microarray data(More)
Previously, over-expression of the long noncoding RNA (lncRNA) HOTAIR has been found to be associated with the invasive and metastatic capacities of several epithelial cancers, including cervical cancer (CaCx). Here, we aimed at identifying functionally relevant genetic variants that may be employed to differentiate between clinically distinct CaCx(More)
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