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HGVS recommendations for the description of sequence variants: 2016 update
JT Den Dunnen, R Dalgleish, DR Maglott, RK Hart, MS Greenblatt, ...
Human mutation 37 (6), 564-569, 2016
16652016
Analysis and application of potential energy smoothing and search methods for global optimization
RV Pappu, RK Hart, JW Ponder
The Journal of Physical Chemistry B 102 (48), 9725-9742, 1998
3171998
GA4GH: International policies and standards for data sharing across genomic research and healthcare
HL Rehm, AJH Page, L Smith, JB Adams, G Alterovitz, LJ Babb, ...
Cell genomics 1 (2), 2021
2012021
Functional characterization of the Bcl-2 gene family in the zebrafish
E Kratz, PM Eimon, K Mukhyala, H Stern, J Zha, A Strasser, R Hart, ...
Cell Death & Differentiation 13 (10), 1631-1640, 2006
1642006
VariantValidator: Accurate validation, mapping, and formatting of sequence variation descriptions
PJ Freeman, RK Hart, LJ Gretton, AJ Brookes, R Dalgleish
Human mutation 39 (1), 61-68, 2018
1432018
An international effort towards developing standards for best practices in analysis, interpretation and reporting of clinical genome sequencing results in the CLARITY Challenge
CA Brownstein, AH Beggs, N Homer, B Merriman, TW Yu, KC Flannery, ...
Genome biology 15, 1-18, 2014
1272014
Somatic cancer variant curation and harmonization through consensus minimum variant level data
DI Ritter, S Roychowdhury, A Roy, S Rao, MJ Landrum, D Sonkin, ...
Genome Medicine 8, 1-9, 2016
682016
The GA4GH variation representation specification: a computational framework for variation representation and federated identification
AH Wagner, L Babb, G Alterovitz, M Baudis, M Brush, DL Cameron, ...
Cell genomics 1 (2), 2021
412021
Exploring the similarities between potential smoothing and simulated annealing
RK Hart, RV Pappu, JW Ponder
Journal of Computational Chemistry 21 (7), 531-552, 2000
412000
Isolation, localization, and physical mapping of a highly polymorphic locus on human chromosome 11q13
JH Eubanks, L Selleri, R Hart, C Rosette, GA Evans
Genomics 11 (3), 720-729, 1991
401991
A Python package for parsing, validating, mapping and formatting sequence variants using HGVS nomenclature
RK Hart, R Rico, E Hare, J Garcia, J Westbrook, VA Fusaro
Bioinformatics 31 (2), 268-270, 2015
382015
CAGI, the Critical Assessment of Genome Interpretation, establishes progress and prospects for computational genetic variant interpretation methods
Genome biology 25 (1), 53, 2024
332024
Systematic and fully automated identification of protein sequence patterns
RK Hart, AK Royyuru, G Stolovitzky, A Califano
Journal of Computational Biology 7 (3-4), 585-600, 2000
322000
hgvs: A Python package for manipulating sequence variants using HGVS nomenclature: 2018 Update
M Wang, KM Callenberg, R Dalgleish, A Fedtsov, NK Fox, PJ Freeman, ...
Human mutation 39 (12), 1803-1813, 2018
232018
Systematic and automated discovery of patterns in PROSITE families
R Hart, AK Royyuru, G Stolovitzky, A Califano
Proceedings of the fourth annual international conference on Computational ¡¦, 2000
202000
SeqRepo: a system for managing local collections of biological sequences
RK Hart, A Prlić
PLoS One 15 (12), e0239883, 2020
112020
ESICM LIVES 2016: part three: Milan, Italy. 1–5 October 2016
T Velasquez, G Mackey, J Lusk, UG Kyle, T Fontenot, P Marshall, ...
Intensive Care Medicine Experimental 4, 405-607, 2016
82016
Unison: an integrated platform for computational biology discovery
RK Hart, K Mukhyala
Biocomputing 2009, 403-414, 2009
72009
Development and application of a computable genotype model in the GA4GH Variation Representation Specification
W Goar, L Babb, S Chamala, M Cline, RR Freimuth, RK Hart, K Kuzma, ...
PACIFIC SYMPOSIUM ON BIOCOMPUTING 2023: Kohala Coast, Hawaii, USA, 3–7 ¡¦, 2022
62022
Pathogenicity interpretation in the Age of precision medicine: the 2015 annual scientific meeting of the human genome variation society
WS Oetting, SE Brenner, AJ Brookes, MS Greenblatt, RK Hart, R Karchin, ...
Human mutation 37 (4), 406, 2016
62016
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