Artikel dengan mandat akses publik - Michael LindermanPelajari lebih lanjut
Tidak tersedia di mana pun: 1
Visualization and cellular hierarchy inference of single-cell data using SPADE
B Anchang, TDP Hart, SC Bendall, P Qiu, Z Bjornson, M Linderman, ...
Nature Protocols 11 (7), 1264-1279, 2016
Mandat: Bill & Melinda Gates Foundation, US National Institutes of Health, Damon …
Tersedia di suatu tempat: 25
Extracting a cellular hierarchy from high-dimensional cytometry data with SPADE
P Qiu, EF Simonds, SC Bendall, KD Gibbs Jr, RV Bruggner, ...
Nature biotechnology 29 (10), 886-891, 2011
Mandat: US National Institutes of Health
Computational solutions to large-scale data management and analysis
EE Schadt, MD Linderman, J Sorenson, L Lee, GP Nolan
Nature Reviews Genetics 11 (9), 647-657, 2010
Mandat: US National Institutes of Health
Genetic fine mapping and genomic annotation defines causal mechanisms at type 2 diabetes susceptibility loci
KJ Gaulton, T Ferreira, Y Lee, A Raimondo, R Mägi, ME Reschen, ...
Nature genetics 47 (12), 1415-1425, 2015
Mandat: US National Institutes of Health, German Research Foundation, Danish Council …
Rethinking data-intensive science using scalable analytics systems
FA Nothaft, M Massie, T Danford, Z Zhang, U Laserson, C Yeksigian, ...
Proceedings of the 2015 ACM SIGMOD International Conference on Management of …, 2015
Mandat: US National Institutes of Health
Motivations, concerns and preferences of personal genome sequencing research participants: Baseline findings from the HealthSeq project
SC Sanderson, MD Linderman, SA Suckiel, GA Diaz, RE Zinberg, ...
European Journal of Human Genetics 24 (1), 14-20, 2016
Mandat: US National Institutes of Health
Development and clinical application of an integrative genomic approach to personalized cancer therapy
AV Uzilov, W Ding, MY Fink, Y Antipin, AS Brohl, C Davis, CY Lau, ...
Genome medicine 8 (1), 62, 2016
Mandat: US National Institutes of Health
Toward clinical genomics in everyday medicine: perspectives and recommendations
SK Delaney, ML Hultner, HJ Jacob, DH Ledbetter, JJ McCarthy, M Ball, ...
Expert review of molecular diagnostics 16 (5), 521-532, 2016
Mandat: US National Institutes of Health
Genetic identification of a common collagen disease in Puerto Ricans via identity-by-descent mapping in a health system
GM Belbin, J Odgis, EP Sorokin, MC Yee, S Kohli, BS Glicksberg, ...
Elife 6, e25060, 2017
Mandat: US National Institutes of Health
Integrated genome-wide association, coexpression network, and expression single nucleotide polymorphism analysis identifies novel pathway in allergic rhinitis
S Bunyavanich, EE Schadt, BE Himes, J Lasky-Su, W Qiu, R Lazarus, ...
BMC medical genomics 7 (1), 48, 2014
Mandat: US National Institutes of Health
Genome-wide association analysis of red blood cell traits in African Americans: the COGENT Network
Z Chen, H Tang, R Qayyum, UM Schick, MA Nalls, R Handsaker, J Li, ...
Human molecular genetics 22 (12), 2529-2538, 2013
Mandat: US National Institutes of Health
Towards program optimization through automated analysis of numerical precision
MD Linderman, M Ho, DL Dill, TH Meng, GP Nolan
Proceedings of the 8th annual IEEE/ACM international symposium on Code …, 2010
Mandat: US National Institutes of Health
Personal Genome Sequencing in Ostensibly Healthy Individuals and the PeopleSeq Consortium
MD Linderman, DE Nielsen, RC Green
Journal of Personalized Medicine 6 (2), 14, 2016
Mandat: US National Institutes of Health, Canadian Institutes of Health Research
Predispositional genome sequencing in healthy adults: design, participant characteristics, and early outcomes of the PeopleSeq Consortium
ES Zoltick, MD Linderman, MA McGinniss, E Ramos, MP Ball, GM Church, ...
Genome Medicine 11 (1), 10, 2019
Mandat: US Department of Defense, US National Institutes of Health, Canadian …
Costs of telaprevir‐based triple therapy for hepatitis C: $189,000 per sustained virological response
K Bichoupan, V Martel‐Laferriere, D Sachs, M Ng, EA Schonfeld, ...
Hepatology 60 (4), 1187-1195, 2014
Mandat: US National Institutes of Health
Novel, Compound Heterozygous, Single‐Nucleotide Variants in MARS2 Associated with Developmental Delay, Poor Growth, and Sensorineural Hearing Loss
BD Webb, PG Wheeler, JJ Hagen, N Cohen, MD Linderman, GA Diaz, ...
Human mutation 36 (6), 587-592, 2015
Mandat: US National Institutes of Health
CytoSPADE: high-performance analysis and visualization of high-dimensional cytometry data
MD Linderman, Z Bjornson, EF Simonds, P Qiu, RV Bruggner, K Sheode, ...
Bioinformatics 28 (18), 2400-2401, 2012
Mandat: US National Institutes of Health
Exome sequencing of extreme clopidogrel response phenotypes identifies B4GALT2 as a determinant of on‐treatment platelet reactivity
SA Scott, JP Collet, U Baber, Y Yang, I Peter, M Linderman, J Sload, ...
Clinical Pharmacology & Therapeutics 100 (3), 287-294, 2016
Mandat: US National Institutes of Health
Concordance between research sequencing and clinical pharmacogenetic genotyping in the eMERGE-PGx study
LJ Rasmussen-Torvik, B Almoguera, KF Doheny, RR Freimuth, ...
The Journal of Molecular Diagnostics 19 (4), 561-566, 2017
Mandat: US National Institutes of Health
Impacts of incorporating personal genome sequencing into graduate genomics education: a longitudinal study over three course years
MD Linderman, SC Sanderson, A Bashir, GA Diaz, A Kasarskis, R Zinberg, ...
BMC Medical Genomics 11 (1), 5, 2018
Mandat: US National Institutes of Health
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