Michael C. Schatz

Orcid: 0000-0002-4118-4446

According to our database1, Michael C. Schatz authored at least 24 papers between 2007 and 2023.

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

Timeline

Legend:

Book 
In proceedings 
Article 
PhD thesis 
Dataset
Other 

Links

On csauthors.net:

Bibliography

2023
Fast and accurate genome-wide predictions and structural modeling of protein-protein interactions using Galaxy.
BMC Bioinform., December, 2023

2022
The Galaxy platform for accessible, reproducible and collaborative biomedical analyses: 2022 update.
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Nucleic Acids Res., 2022

Diversifying the Genomic Data Science Research Community.
CoRR, 2022

Sketching and sampling approaches for fast and accurate long read classification.
BMC Bioinform., 2022

2021
Ribbon: intuitive visualization for complex genomic variation.
Bioinform., 2021

Sapling: accelerating suffix array queries with learned data models.
Bioinform., 2021

2020
Skyhawk: an artificial neural network-based discriminator for reviewing clinically significant genomic variants.
Int. J. Comput. Biol. Drug Des., 2020

Vargas: heuristic-free alignment for assessing linear and graph read aligners.
Bioinform., 2020

2019
Recovering rearranged cancer chromosomes from karyotype graphs.
BMC Bioinform., 2019

2017
GenomeScope: fast reference-free genome profiling from short reads.
Bioinform., 2017

2016
Assemblytics: a web analytics tool for the detection of variants from an assembly.
Bioinform., 2016

NanoBLASTer: Fast alignment and characterization of Oxford Nanopore single molecule sequencing reads.
Proceedings of the 6th IEEE International Conference on Computational Advances in Bio and Medical Sciences, 2016

2014
The contribution of <i>de novo</i> coding mutations to autism spectrum disorder.
Nat., 2014

Answering the demands of digital genomics.
Concurr. Comput. Pract. Exp., 2014

SplitMEM: a graphical algorithm for pan-genome analysis with suffix skips.
Bioinform., 2014

Large-scale Sequencing and Assembly of Cereal Genomes Using Blacklight.
Proceedings of the Annual Conference of the Extreme Science and Engineering Discovery Environment, 2014

On Algorithmic Complexity of Biomolecular Sequence Assembly Problem.
Proceedings of the Algorithms for Computational Biology - First International Conference, 2014

2013
Hawkeye and AMOS: visualizing and assessing the quality of genome assemblies.
Briefings Bioinform., 2013

2012
Genomic dark matter: the reliability of short read mapping illustrated by the genome mappability score.
Bioinform., 2012

2010
Assembly complexity of prokaryotic genomes using short reads.
BMC Bioinform., 2010

2009
Optimizing data intensive GPGPU computations for DNA sequence alignment.
Parallel Comput., 2009

Revealing Biological Modules via Graph Summarization.
J. Comput. Biol., 2009

CloudBurst: highly sensitive read mapping with MapReduce.
Bioinform., 2009

2007
High-throughput sequence alignment using Graphics Processing Units.
BMC Bioinform., 2007


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