Evan K. Maxwell
Evan K. Maxwell
Senior Manager, Data Engineering, Regeneron Genetics Center, Regeneron Pharmaceuticals
Verified email at regeneron.com
Cited by
Cited by
GlycReSoft: A Software Package for Automated Recognition of Glycans from LC/MS Data
E Maxwell, Y Tan, Y Tan, H Hu, G Benson, K Aizikov, S Conley, ...
PLOS ONE 7 (9), e45474, 2012
Global gene expression analysis of murine limb development
L Taher, NM Collette, D Murugesh, E Maxwell, I Ovcharenko, GG Loots
PloS one 6 (12), e28358, 2011
Diagnosing memory leaks using graph mining on heap dumps
EK Maxwell, G Back, N Ramakrishnan
Proceedings of the 16th ACM SIGKDD international conference on Knowledge …, 2010
MicroRNAs and essential components of the microRNA processing machinery are not encoded in the genome of the ctenophore Mnemiopsis leidyi
EK Maxwell, JF Ryan, CE Schnitzler, WE Browne, AD Baxevanis
BMC genomics 13 (1), 1-11, 2012
CLAMMS: a scalable algorithm for calling common and rare copy number variants from exome sequencing data
JS Packer, EK Maxwell, C O’Dushlaine, AE Lopez, FE Dewey, ...
Bioinformatics 32 (1), 133-135, 2016
Whole exome sequencing and characterization of coding variation in 49,960 individuals in the UK Biobank
CV Van Hout, I Tachmazidou, JD Backman, JX Hoffman, B Ye, AK Pandey, ...
BioRxiv, 572347, 2019
Evolutionary profiling reveals the heterogeneous origins of classes of human disease genes: implications for modeling disease genetics in animals
EK Maxwell, CE Schnitzler, P Havlak, NH Putnam, AD Nguyen, ...
BMC evolutionary biology 14 (1), 212, 2014
Profiling and leveraging relatedness in a precision medicine cohort of 92,455 exomes
J Staples, EK Maxwell, N Gosalia, C Gonzaga-Jauregui, C Snyder, ...
The American Journal of Human Genetics 102 (5), 874-889, 2018
SubmiRine: assessing variants in microRNA targets using clinical genomic data sets
EK Maxwell, JD Campbell, A Spira, AD Baxevanis
Nucleic acids research 43 (8), 3886-3898, 2015
Rare-variant pathogenicity triage and inclusion of synonymous variants improves analysis of disease associations of orphan G protein–coupled receptors
R Dershem, RPR Metpally, K Jeffreys, S Krishnamurthy, DT Smelser, ...
Journal of Biological Chemistry 294 (48), 18109-18121, 2019
Profiling copy number variation and disease associations from 50,726 DiscovEHR Study exomes
EK Maxwell, JS Packer, C O’Dushlaine, SE McCarthy, A Hare-Harris, ...
bioRxiv, 119461, 2017
Genetic Variant-Phenotype Analysis System And Methods Of Use
J Reid, O Gottesman, L Habegger, B Cajes, J Staples, E Maxwell
US Patent App. 15/473,302, 2017
Graph mining algorithms for memory leak diagnosis and biological database clustering
EK Maxwell
Virginia Tech, 2010
Methods and systems for detection of abnormal karyotypes
E Maxwell, L Habegger, J Reid
US Patent App. 15/431,715, 2017
KaryoScan: abnormal karyotype detection from whole-exome sequence
EK Maxwell, C Gonzaga-Jauregui, SE McCarthy, C O’Dushlaine, ...
bioRxiv, 204719, 2017
Supplementary Materials for CLAMMS: A Scalable Algorithm for Calling Common and Rare Copy Number Variants from Exome Sequencing Data
JS Packer, EK Maxwell, C O’Dushlaine, AE Lopez, FE Dewey, ...
Bioinformatics Advance Access, 1-24, 2015
Methods And Systems For Copy Number Variant Detection
J Reid, L Habegger, J Packer, E Maxwell
US Patent App. 16/460,420, 2020
Computationally efficient whole genome regression for quantitative and binary traits
J Mbatchou, L Barnard, J Backman, A Marcketta, JA Kosmicki, ...
bioRxiv, 2020
Methods and systems for sparse vector-based matrix transformations
E Maxwell, L Barnard, A Yadav, J Staples, J Reid, L Habegger
US Patent App. 16/428,509, 2019
Methods and systems for copy number variant detection
J Reid, L Habegger, J Packer, E Maxwell
US Patent 10,395,759, 2019
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