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BMC Bioinformatics
|
November 13, 2020
SCELLECTOR: ranking amplification bias in single cells using shallow sequencing
Vivekananda Sarangi, Alexandre Jourdon, Taejeong Bae, et al.
Drug Metabolism and Disposition: the Biological Fate of Chemicals
|
March 4, 2021
<i>SLCO1B1</i>: Application and Limitations of Deep Mutational Scanning for Genomic Missense Variant Function
Lingxin Zhang, Vivekananda Sarangi, Ming-Fen Ho, et al.
Plos One
|
December 21, 2013
SoftSearch: integration of multiple sequence features to identify breakpoints of structural variations
Steven N Hart, Vivekananda Sarangi, Raymond Moore, et al.
Expert Systems with Applications
|
August 27, 2025
Corrigendum to "Identification of gene regulatory networks associated with breast cancer patient survival using an interpretable deep neural network model" [Expert Syst. Appl. 262 (2025) 125632]
Xue Wang, Vivekananda Sarangi, Daniel P Wickland, et al.
Expert Systems with Applications
|
December 16, 2024
Identification of Gene Regulatory Networks Associated with Breast Cancer Patient Survival Using an Interpretable Deep Neural Network Model
Xue Wang, Vivekananda Sarangi, Daniel P Wickland, et al.
Plos Computational Biology
|
April 20, 2022
All2: A tool for selecting mosaic mutations from comprehensive multi-cell comparisons
Vivekananda Sarangi, Yeongjun Jang, Milovan Suvakov, et al.
Plos Computational Biology
|
November 15, 2022
Correction: All2: A tool for selecting mosaic mutations from comprehensive multi-cell comparisons
Vivekananda Sarangi, Yeongjun Jang, Milovan Suvakov, et al.
BMC Medical Genomics
|
June 23, 2021
Frequent POLE-driven hypermutation in ovarian endometrioid cancer revealed by mutational signatures in RNA sequencing
Jaime I Davila, Pritha Chanana, Vivekananda Sarangi, et al.
Clinical and Translational Science
|
February 1, 2020
CYP2C9 and CYP2C19: Deep Mutational Scanning and Functional Characterization of Genomic Missense Variants
Lingxin Zhang, Vivekananda Sarangi, Irene Moon, et al.
Modern Pathology : an Official Journal of the United States and Canadian Academy of Pathology, Inc
|
September 3, 2025
HNF1A-inactived Hepatocellular Adenomas in Fibropolycystic Kidney and Liver Disease Are Associated with Germline HNF1B Variant
Catherine E Hagen, Dipti M Karamchandani, Luisa Ricaurte, et al.
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Search research articles
Search
Showing results (1-10 of 38) with videos related to
Sort By:
Page
of 4
BMC Bioinformatics
|
November 13, 2020
SCELLECTOR: ranking amplification bias in single cells using shallow sequencing
Vivekananda Sarangi, Alexandre Jourdon, Taejeong Bae, et al.
Drug Metabolism and Disposition: the Biological Fate of Chemicals
|
March 4, 2021
<i>SLCO1B1</i>: Application and Limitations of Deep Mutational Scanning for Genomic Missense Variant Function
Lingxin Zhang, Vivekananda Sarangi, Ming-Fen Ho, et al.
Plos One
|
December 21, 2013
SoftSearch: integration of multiple sequence features to identify breakpoints of structural variations
Steven N Hart, Vivekananda Sarangi, Raymond Moore, et al.
Expert Systems with Applications
|
August 27, 2025
Corrigendum to "Identification of gene regulatory networks associated with breast cancer patient survival using an interpretable deep neural network model" [Expert Syst. Appl. 262 (2025) 125632]
Xue Wang, Vivekananda Sarangi, Daniel P Wickland, et al.
Expert Systems with Applications
|
December 16, 2024
Identification of Gene Regulatory Networks Associated with Breast Cancer Patient Survival Using an Interpretable Deep Neural Network Model
Xue Wang, Vivekananda Sarangi, Daniel P Wickland, et al.
Plos Computational Biology
|
April 20, 2022
All2: A tool for selecting mosaic mutations from comprehensive multi-cell comparisons
Vivekananda Sarangi, Yeongjun Jang, Milovan Suvakov, et al.
Plos Computational Biology
|
November 15, 2022
Correction: All2: A tool for selecting mosaic mutations from comprehensive multi-cell comparisons
Vivekananda Sarangi, Yeongjun Jang, Milovan Suvakov, et al.
BMC Medical Genomics
|
June 23, 2021
Frequent POLE-driven hypermutation in ovarian endometrioid cancer revealed by mutational signatures in RNA sequencing
Jaime I Davila, Pritha Chanana, Vivekananda Sarangi, et al.
Clinical and Translational Science
|
February 1, 2020
CYP2C9 and CYP2C19: Deep Mutational Scanning and Functional Characterization of Genomic Missense Variants
Lingxin Zhang, Vivekananda Sarangi, Irene Moon, et al.
Modern Pathology : an Official Journal of the United States and Canadian Academy of Pathology, Inc
|
September 3, 2025
HNF1A-inactived Hepatocellular Adenomas in Fibropolycystic Kidney and Liver Disease Are Associated with Germline HNF1B Variant
Catherine E Hagen, Dipti M Karamchandani, Luisa Ricaurte, et al.
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of 4