Ankit Malhotra
Affiliations: | Jackson Laboratory for Genomic Medicine |
Area:
Genomics, BioinformaticsGoogle:
"Ankit Malhotra"Mean distance: (not calculated yet)
Parents
Sign in to add mentor| Anindya Dutta | grad student | 2003-2010 | UVA | |
| (Computational analysis of high throughout sequencing data - Applications to DNA and RNA studies.) | ||||
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Publications
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| Chaisson MJP, Sanders AD, Zhao X, et al. (2019) Multi-platform discovery of haplotype-resolved structural variation in human genomes. Nature Communications. 10: 1784 |
| Becker T, Lee WP, Leone J, et al. (2018) FusorSV: an algorithm for optimally combining data from multiple structural variation detection methods. Genome Biology. 19: 38 |
| Wang X, Philip VM, Ananda G, et al. (2018) A Bayesian Framework for Generalized Linear Mixed Modeling Identifies New Candidate Loci for Late-Onset Alzheimer's Disease. Genetics |
| Kurum E, Benayoun BA, Malhotra A, et al. (2016) Computational inference of a genomic pluripotency signature in human and mouse stem cells. Biology Direct. 11: 47 |
| Poznik GD, Xue Y, Mendez FL, et al. (2016) Punctuated bursts in human male demography inferred from 1,244 worldwide Y-chromosome sequences. Nature Genetics |
| Menghi F, Inaki K, Woo X, et al. (2016) The tandem duplicator phenotype as a distinct genomic configuration in cancer. Proceedings of the National Academy of Sciences of the United States of America |
| Sudmant PH, Rausch T, Gardner EJ, et al. (2015) An integrated map of structural variation in 2,504 human genomes. Nature. 526: 75-81 |
| Qin W, Dion SL, Kutny PM, et al. (2015) Efficient CRISPR/Cas9-Mediated Genome Editing in Mice by Zygote Electroporation of Nuclease. Genetics. 200: 423-30 |
| Malhotra A, Wang Y, Waters J, et al. (2015) Ploidy-Seq: inferring mutational chronology by sequencing polyploid tumor subpopulations. Genome Medicine. 7: 6 |
| Inaki K, Menghi F, Woo XY, et al. (2014) Systems consequences of amplicon formation in human breast cancer. Genome Research. 24: 1559-71 |