Michael I. Love

Orcid: 0000-0001-8401-0545

According to our database1, Michael I. Love authored at least 18 papers between 2012 and 2024.

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Bibliography

2024
Perceptual and technical barriers in sharing and formatting metadata accompanying omics studies.
CoRR, 2024

2023
Comprehensive evaluation of methods for differential expression analysis of metatranscriptomics data.
Briefings Bioinform., September, 2023

bootRanges: flexible generation of null sets of genomic ranges for hypothesis testing.
Bioinform., May, 2023

matchRanges: generating null hypothesis genomic ranges via covariate-matched sampling.
Bioinform., May, 2023

excluderanges: exclusion sets for T2T-CHM13, GRCm39, and other genome assemblies.
Bioinform., April, 2023

2022
Airpart: interpretable statistical models for analyzing allelic imbalance in single-cell datasets.
Bioinform., 2022

Plotgardener: cultivating precise multi-panel figures in R.
Bioinform., 2022

2021
Compression of quantification uncertainty for scRNA-seq counts.
Bioinform., 2021

An approach for normalization and quality control for NanoString RNA expression data.
Briefings Bioinform., 2021

2020
Tximeta: Reference sequence checksums for provenance identification in RNA-seq.
PLoS Comput. Biol., 2020

Finding Stable Groups of Cross-Correlated Features in Multi-View data.
CoRR, 2020

Terminus enables the discovery of data-driven, robust transcript groups from RNA-seq data.
Bioinform., 2020

Consistency and overfitting of multi-omics methods on experimental data.
Briefings Bioinform., 2020

2019
Heavy-tailed prior distributions for sequence count data: removing the noise and preserving large differences.
Bioinform., 2019

SAFE-clustering: Single-cell Aggregated (from Ensemble) clustering for single-cell RNA-seq data.
Bioinform., 2019

2018
coTRaCTE predicts co-occurring transcription factors within cell-type specific enhancers.
PLoS Comput. Biol., 2018

Swimming downstream: statistical analysis of differential transcript usage following Salmon quantification.
F1000Research, 2018

2012
Breakpointer: using local mapping artifacts to support sequence breakpoint discovery from single-end reads.
Bioinform., 2012


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