Jain, Dhawal

Comprehensive analysis of chromothripsis in 2,658 human cancers using whole-genome sequencing

Cortés-Ciriano, I., Lee, J. J.-K., Xi, R., Jain, D., Jung, Y. L., Yang, L., Gordenin, D., Klimczak, L. J., Zhang, C.-Z., Pellman, D. S., et al. (2020) · Nature Genetics

Cancer Genomics and DiagnosticsGenomic variations and chromosomal abnormalities

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Active promoters give rise to false positive ‘Phantom Peaks’ in ChIP-seq experiments

Jain, D., Baldi, S., Zabel, A., Straub, T., & Becker, P. B. (2015) · Nucleic Acids Research

Genomics and Chromatin DynamicsChromatin Remodeling and Cancer

Cited by 156

HiNT: a computational method for detecting copy number variations and translocations from Hi-C data

Wang, S., Lee, S., Chu, C., Jain, D., Kerpedjiev, P., Nelson, G. M., Walsh, J. M., Alver, B. H., & Park, P. J. (2020) · Genome Biology

Genomic variations and chromosomal abnormalitiesGenomics and Chromatin Dynamics

Cited by 99