ScholarGate
Assistent

Methoden vergleichen

Prüfen Sie die ausgewählten Methoden nebeneinander; abweichende Zeilen sind hervorgehoben.

Bayesian Single-Cell RNA-seq Analysis×Variationaler Autoencoder×
FachgebietBioinformatikDeep Learning
FamilieProcess / pipelineMachine learning
Entstehungsjahr2018 (scVI landmark); Bayesian scRNA-seq approaches emerged 2015-20182014
UrheberRomain Lopez, Nir Yosef and Michael I. Jordan (scVI framework); preceded by Bayesian single-cell methods from Kharchenko, Markowetz, and othersKingma, D. P. & Welling, M.
TypProbabilistic generative modeling pipelineDeep generative latent-variable model (encoder–decoder)
Wegweisende QuelleLopez, R., Regier, J., Cole, M. B., Jordan, M. I., & Yosef, N. (2018). Deep generative modeling for single-cell transcriptomics. Nature Methods, 15(12), 1053-1058. DOI ↗Kingma, D. P. & Welling, M. (2014). Auto-Encoding Variational Bayes. International Conference on Learning Representations (ICLR). link ↗
AliasnamenBayesian scRNA-seq, scRNA-seq Bayesian modeling, probabilistic single-cell transcriptomics, Bayesian single-cell genomicsDeğişkensel Otokodlayıcı (VAE), VAE, auto-encoding variational Bayes, deep latent variable model
Verwandt35
ZusammenfassungBayesian single-cell RNA-seq analysis applies probabilistic generative models to the sparse, overdispersed count matrices produced by single-cell RNA sequencing. By placing prior distributions over latent biological variables — cell state, batch effects, dropout — the framework propagates uncertainty through every downstream inference step. Tools such as scVI, SCVI-tools, and BayesPrism implement this paradigm, enabling principled cell clustering, differential expression testing, and batch integration that explicitly models technical noise rather than ignoring it.The Variational Autoencoder (VAE) is a deep generative latent-variable model, introduced by Diederik Kingma and Max Welling in 2014, that encodes data as a probability distribution in a latent space and samples from that distribution to generate new examples. It is used for data generation, anomaly detection, and feature learning.
ScholarGateDatensatz
  1. v1
  2. 2 Quellen
  3. PUBLISHED
  1. v1
  2. 2 Quellen
  3. PUBLISHED

Zur Suche Folien herunterladen

ScholarGateMethoden vergleichen: Bayesian single-cell RNA-seq analysis · Variational Autoencoder. Abgerufen am 2026-06-15 von https://scholargate.app/de/compare