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Jonathan K. Pritchard
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2020 – today
- 2024
- [c4]Romain Lopez, Jan-Christian Hütter, Ehsan Hajiramezanali, Jonathan K. Pritchard, Aviv Regev:
Toward the Identifiability of Comparative Deep Generative Models. CLeaR 2024: 868-912 - [i3]Romain Lopez, Jan-Christian Hütter, Ehsan Hajiramezanali, Jonathan K. Pritchard, Aviv Regev:
Toward the Identifiability of Comparative Deep Generative Models. CoRR abs/2401.15903 (2024) - 2023
- [c3]Romain Lopez, Natasa Tagasovska, Stephen Ra, Kyunghyun Cho, Jonathan K. Pritchard, Aviv Regev:
Learning Causal Representations of Single Cells via Sparse Mechanism Shift Modeling. CLeaR 2023: 662-691 - 2022
- [c2]Romain Lopez, Jan-Christian Hütter, Jonathan K. Pritchard, Aviv Regev:
Large-Scale Differentiable Causal Discovery of Factor Graphs. NeurIPS 2022 - [i2]Romain Lopez, Jan-Christian Hütter, Jonathan K. Pritchard, Aviv Regev:
Large-Scale Differentiable Causal Discovery of Factor Graphs. CoRR abs/2206.07824 (2022) - [i1]Romain Lopez, Natasa Tagasovska, Stephen Ra, Kyunghyun Cho, Jonathan K. Pritchard, Aviv Regev:
Learning Causal Representations of Single Cells via Sparse Mechanism Shift Modeling. CoRR abs/2211.03553 (2022)
2010 – 2019
- 2017
- [j5]Eilon Sharon
, Hao Shi
Quantification of transplant-derived circulating cell-free DNA in absence of a donor genotype. PLoS Comput. Biol. 13(8) (2017) - 2011
- [j4]Joseph K. Pickrell, Daniel J. Gaffney
False positive peaks in ChIP-seq and other sequencing-based functional assays caused by unannotated high copy number regions. Bioinform. 27(15): 2144-2146 (2011) - [j3]Páll Melsted
Efficient counting of k-mers in DNA sequences using a Bloom Filter. BMC Bioinform. 12: 333 (2011)
2000 – 2009
- 2009
- [j2]Jacob F. Degner, John C. Marioni
Effect of read-mapping biases on detecting allele-specific expression from RNA-sequencing data. Bioinform. 25(24): 3207-3212 (2009) - 2005
- [j1]Sebastian Zöllner, Xiaoquan Wen
Association mapping and fine mapping with TreeLD. Bioinform. 21(14): 3168-3170 (2005) - 2002
- [c1]Sebastian Zöllner, Jonathan K. Pritchard:
A Coalescent-Based Approach for Complex Disease Mapping. Computational Methods for SNPs and Haplotype Inference 2002: 124-130
Coauthor Index
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last updated on 2024-05-14 21:21 CEST by the dblp team
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