Found: 11
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Missing data and technical variability in single-cell RNA-sequencing experiments.
- Published in:
- 2018
- By:
- Publication type:
- journal article
Telescoping bimodal latent Dirichlet allocation to identify expression QTLs across tissues.
- Published in:
- Life Science Alliance, 2022, v. 5, n. 12, p. 1, doi. 10.26508/lsa.202101297
- By:
- Publication type:
- Article
Identifying longevity associated genes by integrating gene expression and curated annotations.
- Published in:
- PLoS Computational Biology, 2020, v. 16, n. 11, p. 1, doi. 10.1371/journal.pcbi.1008429
- By:
- Publication type:
- Article
Predicting Subnational Ebola Virus Disease Epidemic Dynamics from Sociodemographic Indicators.
- Published in:
- PLoS ONE, 2016, v. 11, n. 10, p. 1, doi. 10.1371/journal.pone.0163544
- By:
- Publication type:
- Article
Thermal Preference and Species Range in Mountaintop Salamanders and Their Widespread Competitors.
- Published in:
- Journal of Herpetology, 2019, v. 53, n. 2, p. 96, doi. 10.1670/18-110
- By:
- Publication type:
- Article
Cerebellar contributions to a brainwide network for flexible behavior in mice.
- Published in:
- Communications Biology, 2023, v. 6, n. 1, p. 1, doi. 10.1038/s42003-023-04920-0
- By:
- Publication type:
- Article
Author Correction: Feature selection and dimension reduction for single-cell RNA-Seq based on a multinomial model.
- Published in:
- 2020
- By:
- Publication type:
- Correction Notice
Quantile normalization of single-cell RNA-seq read counts without unique molecular identifiers.
- Published in:
- Genome Biology, 2020, v. 21, n. 1, p. 1, doi. 10.1186/s13059-020-02078-0
- By:
- Publication type:
- Article
Feature selection and dimension reduction for single-cell RNA-Seq based on a multinomial model.
- Published in:
- Genome Biology, 2019, v. 20, n. 1, p. 1, doi. 10.1186/s13059-019-1861-6
- By:
- Publication type:
- Article
Family‐based tests for associating haplotypes with general phenotype data.
- Published in:
- Genetic Epidemiology, 2018, v. 42, n. 1, p. 123, doi. 10.1002/gepi.22094
- By:
- Publication type:
- Article
A unifying framework for rare variant association testing in family-based designs, including higher criticism approaches, SKATs, and burden tests.
- Published in:
- Bioinformatics, 2020, v. 36, n. 22/23, p. 5432, doi. 10.1093/bioinformatics/btaa1055
- By:
- Publication type:
- Article