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Hannah Carter
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2020 – today
- 2024
- [j9]Eve Richardson
, Raphael Trevizani, Jason A. Greenbaum, Hannah Carter, Morten Nielsen, Bjoern Peters:
The receiver operating characteristic curve accurately assesses imbalanced datasets. Patterns 5(6): 100994 (2024) - 2023
- [j8]Zeynep Kosaloglu-Yalçin
The Cancer Epitope Database and Analysis Resource (CEDAR). Nucleic Acids Res. 51(D1): 845-852 (2023) - [j7]Adam R. Klie
Predictive analyses of regulatory sequences with EUGENe. Nat. Comput. Sci. 3(11): 946-956 (2023) - 2021
- [j6]Adam R. Klie
Increasing metadata coverage of SRA BioSample entries using deep learning-based named entity recognition. Database J. Biol. Databases Curation 2021 (2021)
2010 – 2019
- 2019
- [j5]Alexandra R. Buckley, Trey Ideker
Rare variant phasing using paired tumor: normal sequence data. BMC Bioinform. 20(1): 265:1-265:11 (2019) - [c4]Rachel M. Pyke, Raphael Genolet, Alexandre Harari, George Coukos, David Gfeller, Hannah Carter:
Computational KIR copy number discovery reveals interaction between inhibitory receptor burden and survival. PSB 2019: 148-159 - [c3]Brian Tsui, Michelle Dow, Dylan Skola, Hannah Carter:
Extracting allelic read counts from 250, 000 human sequencing runs in Sequence Read Archive. PSB 2019: 196-207 - 2018
- [c2]Billur Engin, Matan Hofree, Hannah Carter:
Erratum: Identifying mutation specific cancer pathways using a structurally resolved protein interaction network. PSB 2018: 634 - 2015
- [c1]Billur Engin, Matan Hofree, Hannah Carter:
Identifying Mutation Specific Cancer Pathways Using a Structurally Resolved Protein Interaction Network. Pacific Symposium on Biocomputing 2015: 84-95 - 2014
- [j4]Yun-Ching Chen, Christopher Douville, Cheng Wang, Noushin Niknafs, Grace H. T. Yeo
A Probabilistic Model to Predict Clinical Phenotypic Traits from Genome Sequencing. PLoS Comput. Biol. 10(9) (2014) - 2013
- [j3]Christopher Douville, Hannah Carter, Rick Kim, Noushin Niknafs, Mark Diekhans
CRAVAT: cancer-related analysis of variants toolkit. Bioinform. 29(5): 647-648 (2013) - 2011
- [j2]Wing Chung Wong, Dewey Kim, Hannah Carter, Mark Diekhans
CHASM and SNVBox: toolkit for detecting biologically important single nucleotide mutations in cancer. Bioinform. 27(15): 2147-2148 (2011)
2000 – 2009
- 2009
- [j1]Ursula Pieper
MODBASE, a database of annotated comparative protein structure models and associated resources. Nucleic Acids Res. 37(Database-Issue): 347-354 (2009)
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