Colin C. Collins

Affiliations:
  • Vancouver Prostate Centre, BC, Canada
  • University of British Columbia, Department of Urologic Sciences, Vancouver, BC, Canada


According to our database1, Colin C. Collins authored at least 22 papers between 2003 and 2024.

Collaborative distances:

Timeline

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Bibliography

2024
Phenotype prediction from single-cell RNA-seq data using attention-based neural networks.
Bioinform., February, 2024

2021
Out-of-distribution generalization from labelled and unlabelled gene expression data for drug response prediction.
Nat. Mach. Intell., 2021

2020
AITL: Adversarial Inductive Transfer Learning with input and output space adaptation for pharmacogenomics.
Bioinform., 2020

Identification of conserved evolutionary trajectories in tumors.
Bioinform., 2020

CircMiner: accurate and rapid detection of circular RNA through splice-aware pseudo-alignment scheme.
Bioinform., 2020

2019
MOLI: multi-omics late integration with deep neural networks for drug response prediction.
Bioinform., 2019

Alignment-free clustering of UMI tagged DNA molecules.
Bioinform., 2019

2018
Computational identification of micro-structural variations and their proteogenomic consequences in cancer.
Bioinform., 2018

MechRNA: prediction of lncRNA mechanisms from RNA-RNA and RNA-protein interactions.
Bioinform., 2018

2017
Clonality Inference from Single Tumor Samples Using Low-Coverage Sequence Data.
J. Comput. Biol., 2017

SiNVICT: ultra-sensitive detection of single nucleotide variants and indels in circulating tumour DNA.
Bioinform., 2017

2014
ShatterProof: operational detection and quantification of chromothripsis.
BMC Bioinform., 2014

ORMAN: Optimal resolution of ambiguous RNA-Seq multimappings in the presence of novel isoforms.
Bioinform., 2014

HIT'nDRIVE: Multi-driver Gene Prioritization Based on Hitting Time.
Proceedings of the Research in Computational Molecular Biology, 2014

2012
Dissect: detection and characterization of novel structural alterations in transcribed sequences.
Bioinform., 2012

CLIIQ: Accurate Comparative Detection and Quantification of Expressed Isoforms in a Population.
Proceedings of the Algorithms in Bioinformatics - 12th International Workshop, 2012

Discovery of Complex Genomic Rearrangements in Cancer Using High-Throughput Sequencing.
Proceedings of the Research in Computational Molecular Biology, 2012

2011
Detection of recurrent rearrangement breakpoints from copy number data.
BMC Bioinform., 2011

Comrad: detection of expressed rearrangements by integrated analysis of RNA-Seq and low coverage genome sequence data.
Bioinform., 2011

Optimally discriminative subnetwork markers predict response to chemotherapy.
Bioinform., 2011

2008
Evaluation of Paired-End Sequencing Strategies for Detection of Genome Rearrangements in Cancer.
PLoS Comput. Biol., 2008

2003
Reconstructing tumor genome architectures.
Proceedings of the European Conference on Computational Biology (ECCB 2003), 2003


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