Benedict Paten

Orcid: 0000-0001-8863-3539

According to our database1, Benedict Paten authored at least 48 papers between 2009 and 2023.

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Bibliography

2023
Building a collaborative cloud platform to accelerate heart, lung, blood, and sleep research.
J. Am. Medical Informatics Assoc., June, 2023

Optimal gap-affine alignment in <i>O</i>(<i>s</i>) space.
Bioinform., February, 2023

GENCODE: reference annotation for the human and mouse genomes in 2023.
Nucleic Acids Res., January, 2023

Genetic Site-Aware Three-Dimensional Layout Algorithm for Variation Graphs.
Proceedings of the 14th ACM International Conference on Bioinformatics, 2023

2022
GBZ file format for pangenome graphs.
Bioinform., November, 2022

2021
The Dockstore: enhancing a community platform for sharing reproducible and accessible computational protocols.
Nucleic Acids Res., 2021

GENCODE 2021.
Nucleic Acids Res., 2021

Efficient dynamic variation graphs.
Bioinform., 2021

The Immersive Graph Genome Explorer: Navigating Genomics in Immersive Virtual Reality.
Proceedings of the 9th IEEE International Conference on Serious Games and Applications for Health, 2021

Walk-Preserving Transformation of Overlapped Sequence Graphs into Blunt Sequence Graphs with GetBlunted.
Proceedings of the Connecting with Computability, 2021

2020
BioHackathon 2015: Semantics of data for life sciences and reproducible research.
F1000Research, 2020

Haplotype-aware graph indexes.
Bioinform., 2020

Gaussian mixture model-based unsupervised nucleotide modification number detection using nanopore-sequencing readouts.
Bioinform., 2020

Distance indexing and seed clustering in sequence graphs.
Bioinform., 2020

SegAlign: a scalable GPU-based whole genome aligner.
Proceedings of the International Conference for High Performance Computing, 2020

2019
The human body at cellular resolution: the NIH Human Biomolecular Atlas Program.
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Nat., 2019

GENCODE reference annotation for the human and mouse genomes.
Nucleic Acids Res., 2019

Sequence tube maps: making graph genomes intuitive to commuters.
Bioinform., 2019

An average-case sublinear forward algorithm for the haploid Li and Stephens model.
Algorithms Mol. Biol., 2019

DP-CGAN: Differentially Private Synthetic Data and Label Generation.
Proceedings of the IEEE Conference on Computer Vision and Pattern Recognition Workshops, 2019

2018
Superbubbles, Ultrabubbles, and Cacti.
J. Comput. Biol., 2018

A Flow Procedure for Linearization of Genome Sequence Graphs.
J. Comput. Biol., 2018

An Average-Case Sublinear Exact Li and Stephens Forward Algorithm.
Proceedings of the 18th International Workshop on Algorithms in Bioinformatics, 2018

2017
Developing a framework for digital objects in the Big Data to Knowledge (BD2K) commons: Report from the Commons Framework Pilots workshop.
J. Biomed. Informatics, 2017

The Dockstore: enabling modular, community-focused sharing of Docker-based genomics tools and workflows.
F1000Research, 2017

Modelling haplotypes with respect to reference cohort variation graphs.
Bioinform., 2017

A graph extension of the positional Burrows-Wheeler transform and its applications.
Algorithms Mol. Biol., 2017

Superbubbles, Ultrabubbles and Cacti.
Proceedings of the Research in Computational Molecular Biology, 2017

A Flow Procedure for the Linearization of Genome Sequence Graphs.
Proceedings of the Research in Computational Molecular Biology, 2017

Data Sharing and Reproducible Clinical Genetic Testing: Successes and Challenges.
Proceedings of the Biocomputing 2017: Proceedings of the Pacific Symposium, 2017

Count Everything: Secure Count Query Framework Across Big Data Centers.
Proceedings of the Summit on Clinical Research Informatics, 2017

Describing the Local Structure of Sequence Graphs.
Proceedings of the Algorithms for Computational Biology, 2017

2016
The UCSC Genome Browser database: 2016 update.
Nucleic Acids Res., 2016

Representing and decomposing genomic structural variants as balanced integer flows on sequence graphs.
BMC Bioinform., 2016

2015
The UCSC Genome Browser database: 2015 update.
Nucleic Acids Res., 2015

Building a Pan-Genome Reference for a Population.
J. Comput. Biol., 2015

The NIH BD2K center for big data in translational genomics.
J. Am. Medical Informatics Assoc., 2015

MinION Analysis and Reference Consortium: Phase 1 data release and analysis.
F1000Research, 2015

Canonical, stable, general mapping using context schemes.
Bioinform., 2015

2014
A unifying model of genome evolution under parsimony.
BMC Bioinform., 2014

Track data hubs enable visualization of user-defined genome-wide annotations on the UCSC Genome Browser.
Bioinform., 2014

Comparative assembly hubs: Web-accessible browsers for comparative genomics.
Bioinform., 2014

Ragout - a reference-assisted assembly tool for bacterial genomes.
Bioinform., 2014

Building a Pangenome Reference for a Population.
Proceedings of the Research in Computational Molecular Biology, 2014

2013
HAL: a hierarchical format for storing and analyzing multiple genome alignments.
Bioinform., 2013

2011
Cactus Graphs for Genome Comparisons.
J. Comput. Biol., 2011

Meta-Alignment with Crumble and Prune: Partitioning very large alignment problems for performance and parallelization.
BMC Bioinform., 2011

2009
Sequence progressive alignment, a framework for practical large-scale probabilistic consistency alignment.
Bioinform., 2009


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