Zachary B. Abrams

Orcid: 0000-0001-5219-9996

According to our database1, Zachary B. Abrams authored at least 21 papers between 2015 and 2024.

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

Timeline

Legend:

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PhD thesis 
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Links

On csauthors.net:

Bibliography

2024
Document-level Clinical Entity and Relation extraction via Knowledge Base-Guided Generation.
Proceedings of the 23rd Workshop on Biomedical Natural Language Processing, 2024

2023
Electronic health record data quality assessment and tools: a systematic review.
J. Am. Medical Informatics Assoc., September, 2023

2022
Self-explaining neural network with concept-based explanations for ICU mortality prediction.
Proceedings of the BCB '22: 13th ACM International Conference on Bioinformatics, Computational Biology and Health Informatics, Northbrook, Illinois, USA, August 7, 2022

2021
Simulation-derived best practices for clustering clinical data.
J. Biomed. Informatics, 2021

Pattern recognition in lymphoid malignancies using CytoGPS and Mercator.
BMC Bioinform., 2021

RCytoGPS: an R package for reading and visualizing cytogenetics data.
Bioinform., 2021

Mercator: a pipeline for multi-method, unsupervised visualization and distance generation.
Bioinform., 2021

2020
Explaining Gene Expression Using Twenty-One MicroRNAs.
J. Comput. Biol., 2020

Unsupervised machine learning and prognostic factors of survival in chronic lymphocytic leukemia.
J. Am. Medical Informatics Assoc., 2020

Umpire 2.0: Simulating realistic, mixed-type, clinical data for machine learning.
F1000Research, 2020

CytoGPS: A Web-Enabled Karyotype Analysis Tool for Cytogeneticists and Biomedical Data Scientists.
Proceedings of the AMIA 2020, 2020

2019
A protocol to evaluate RNA sequencing normalization methods.
BMC Bioinform., 2019

Inferring clonal heterogeneity in cancer using SNP arrays and whole genome sequencing.
Bioinform., 2019

CytoGPS: a web-enabled karyotype analysis tool for cytogenetics.
Bioinform., 2019

2018
Thresher: determining the number of clusters while removing outliers.
BMC Bioinform., 2018

2017
Mapping Neuronal Cell Types Using Integrative Multi-Species Modeling of Human and Mouse Single Cell RNA Sequencing.
Proceedings of the Biocomputing 2017: Proceedings of the Pacific Symposium, 2017

2016
Session Introduction.
Proceedings of the Biocomputing 2016: Proceedings of the Pacific Symposium, 2016

Using Karyotype Data for Automated Disease Classification: A Proof of Concept Demonstration.
Proceedings of the Summit on Clinical Research Informatics, 2016

Use of Administrative Data to Predict Risk of Liver Disease.
Proceedings of the Summit on Clinical Research Informatics, 2016

2015
Text Mining and Data Modeling of Karyotypes to aid in Drug Repurposing Efforts.
Proceedings of the MEDINFO 2015: eHealth-enabled Health, 2015

KaryoViz: Designing A Karyotype Visualization Platform for Clinical Decision Support.
Proceedings of the AMIA 2015, 2015


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