Andrew D. Smith

Orcid: 0000-0002-3337-1970

According to our database1, Andrew D. Smith authored at least 32 papers between 2003 and 2023.

Collaborative distances:
  • Dijkstra number2 of four.
  • Erdős number3 of four.

Timeline

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Links

On csauthors.net:

Bibliography

2023
Pulmonary Surface Irregularity Score as a New Quantitative CT Marker for Idiopathic Pulmonary Fibrosis - a Pilot Study.
J. Digit. Imaging, December, 2023

Counting Distinguishable RNA Secondary Structures.
J. Comput. Biol., October, 2023

2022
On attainability of Kendall's tau matrices and concordance signatures.
J. Multivar. Anal., 2022

Artificial Intelligence in Perioperative Medicine: A Proposed Common Language With Applications to FDA-Approved Devices.
Frontiers Digit. Health, 2022

2020
Predicting the Number of Bases to Attain Sufficient Coverage in High-Throughput Sequencing Experiments.
J. Comput. Biol., 2020

Accurate detection of short and long active ORFs using Ribo-seq data.
Bioinform., 2020

2018
A tool to visualize and analyze perfusion data: Development and application of the R package "CTP".
Comput. Methods Programs Biomed., 2018

2017
Riborex: fast and flexible identification of differential translation from Ribo-seq data.
Bioinform., 2017

2016
WALT: fast and accurate read mapping for bisulfite sequencing.
Bioinform., 2016

2015
Applications of species accumulation curves in large-scale biological data analysis.
Quant. Biol., 2015

2014
Using beta-binomial regression for high-precision differential methylation analysis in multifactor whole-genome bisulfite sequencing experiments.
BMC Bioinform., 2014

Modeling genome coverage in single-cell sequencing.
Bioinform., 2014

The Amordad database engine for metagenomics.
Bioinform., 2014

2013
A Geometric Interpretation for Local Alignment-Free Sequence Comparison.
J. Comput. Biol., 2013

MLML: consistent simultaneous estimates of DNA methylation and hydroxymethylation.
Bioinform., 2013

2012
Site identification in high-throughput RNA-protein interaction data.
Bioinform., 2012

2011
Multiple Sequence Assembly from Reads Alignable to a Common Reference Genome.
IEEE ACM Trans. Comput. Biol. Bioinform., 2011

Identifying dispersed epigenomic domains from ChIP-Seq data.
Bioinform., 2011

2009
Challenges in Understanding Genome-Wide DNA Methylation.
J. Comput. Sci. Technol., 2009

Gene set-based module discovery in the breast cancer transcriptome.
BMC Bioinform., 2009

Updates to the RMAP short-read mapping software.
Bioinform., 2009

2008
Using quality scores and longer reads improves accuracy of Solexa read mapping.
BMC Bioinform., 2008

Integrative bioinformatics analysis of transcriptional regulatory programs in breast cancer cells.
BMC Bioinform., 2008

2007
Statistical significance of cis-regulatory modules.
BMC Bioinform., 2007

Computational prediction of novel components of lung transcriptional networks.
Bioinform., 2007

2005
SIMPROT: Using an empirically determined indel distribution in simulations of protein evolution.
BMC Bioinform., 2005

DWE: Discriminating Word Enumerator.
Bioinform., 2005

Mining ChIP-chip data for transcription factor and cofactor binding sites.
Proceedings of the Proceedings Thirteenth International Conference on Intelligent Systems for Molecular Biology 2005, 2005

2003
On the complexity of finding common approximate substrings.
Theor. Comput. Sci., 2003

A Transition Probability Model for Amino Acid Substitutions from Blocks.
J. Comput. Biol., 2003

Toward Optimal Motif Enumeration.
Proceedings of the Algorithms and Data Structures, 8th International Workshop, 2003

Complexity of Approximating Closest Substring Problems.
Proceedings of the Fundamentals of Computation Theory, 14th International Symposium, 2003


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