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Vartika Agrawal
Vartika Agrawal
10x Genomics
Verified email at 10xgenomics.com
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Cited by
Cited by
Year
Exome sequencing of patients with histiocytoid cardiomyopathy reveals a de novo NDUFB11 mutation that plays a role in the pathogenesis of histiocytoid …
BM Shehata, CA Cundiff, K Lee, A Sabharwal, MK Lalwani, AK Davis, ...
American Journal of Medical Genetics Part A 167 (9), 2114-2121, 2015
352015
Omic personality: implications of stable transcript and methylation profiles for personalized medicine
R Tabassum, A Sivadas, V Agrawal, H Tian, D Arafat, G Gibson
Genome medicine 7 (1), 1-17, 2015
142015
Genomic informatics service
N Dimitrova, WK Carey, RJ Krasinski, J Nilsson, B Grantham, ...
US Patent 10,528,758, 2020
62020
Secure transmission of genomic data
V Agrawal, N Dimitrova, RJ Krasinski
US Patent 10,957,420, 2021
42021
Relevance feedback to improve the performance of clustering model that clusters patients with similar profiles together
V Agrawal, AR Mankovich, N Dimitrova, N Banerjee, YH Cheung, ...
US Patent App. 16/084,800, 2019
22019
Securing Genomic Computations for Research and Clinical Decision Support
K Carey, N Dimitrova, B Grantham, V Agrawal, J Nilsson, R Krasinski
1st PETS Workshop on Genome Privacy (GenoPri), 2014
22014
Method and apparatus for masking clinically irrelevant ancestry information in genetic data
V Agrawal
US Patent App. 16/500,459, 2020
12020
PAPAyA: A Highly Scalable Cloud-based Framework for Genomic Processing.
F Andry, N Dimitrova, A Mankovich, V Agrawal, A Bder, A David
BIOINFORMATICS, 198-206, 2016
12016
Abstract P4-04-07: Heterogeneous gene fusions detected by RNASeq show enrichment of insulin signaling pathway genes in breast cancer
V Varadan, V Agrawal, S Kamalakaran, N Banerjee, K Miskimen, ...
Cancer Research 73 (24_Supplement), P4-04-07-P4-04-07, 2013
12013
Method for assessing genome alignment basis
V Agrawal
US Patent App. 17/272,517, 2021
2021
Systems and methods for prioritizing variants of unknown significance
V Agrawal, N Dimitrova
US Patent 10,734,095, 2020
2020
A method and apparatus for collaborative variant selection and therapy matching reporting
N Dimitrova, R Solomon, K Payal, M Danisman-Tasar, M Bentzur, ...
US Patent App. 16/336,246, 2020
2020
Sub-population detection and quantization of receptor-ligand states for characterizing inter-cellular communication and intratumoral heterogeneity
BS Santhanam, YH Cheung, V Agrawal, JM De Bont, N Dimitrova
US Patent App. 16/093,696, 2019
2019
Systems and methods for prioritizing variants of unknown significance
V Agrawal, N Dimitrova
US Patent App. 15/747,279, 2018
2018
Abstract P2-05-06: Not presented
V Agrawal, YH Cheung, P Keswarpu, G Somlo, M Abu-Khalaf, W Sikov, ...
Cancer Research 78 (4_Supplement), P2-05-06-P2-05-06, 2018
2018
Methods and systems for visualizing gene expression data
AR Mankovich, N Dimitrova, V Agrawal, N Banerjee
US Patent App. 15/507,275, 2017
2017
RNA-Seq to reveal mitochondrial gene fusions in breast cancer.
V Agrawal, YH Cheung, P Keswarpu, G Somlo, M Abu-Khalaf, WM Sikov, ...
Journal of Clinical Oncology 35 (15_suppl), e13019-e13019, 2017
2017
Abstract P1-05-29: Genomic variants in 5 male breast cancers using whole exome sequencing
V Agrawal, M Zhong, W Huang, P Kewarpu, N Dimitrova, JT Fallon
Cancer Research 77 (4_Supplement), P1-05-29-P1-05-29, 2017
2017
Validation of an Amplicon-Based NGS Cancer Panel and Informatics Pipeline as Potential Replacement for Sanger and PCR-Based Methods for Somatic Mutation Detection in a Hospital …
M Zhong, A Mankovich, J Zhuge, Y Mao, W Huang, G Wang, V Agrawal, ...
JOURNAL OF MOLECULAR DIAGNOSTICS 18 (6), 1005-1005, 2016
2016
Dissecting components of intercellular communication in a heterogeneous tumor
B Santhanam, YH Cheung, V Agrawal, K Volyanskyy, N Dimitrova
Cancer Research 76 (14_Supplement), 170-170, 2016
2016
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