[HTML][HTML] Reference-free inferring of transcriptomic events in cancer cells on single-cell data

B Eralp, E Sefer - BMC cancer, 2024 - Springer
Background Cancerous cells' identity is determined via a mixture of multiple factors such as
genomic variations, epigenetics, and the regulatory variations that are involved in …

Clustering malignant cell states using universally variable genes

SH Yoon, JW Nam - Briefings in Bioinformatics, 2024 - academic.oup.com
Single-cell RNA sequencing (scRNA-seq) has revealed important insights into the
heterogeneity of malignant cells. However, sample-specific genomic alterations often …

CanSig: discovery of shared transcriptional states across cancer patients from single-cell RNA sequencing data

J Yates, F Barkmann, P Czyz, A Kraft, M Glettig… - bioRxiv, 2022 - biorxiv.org
Multiple cancer types have been shown to exhibit heterogeneity in the transcriptional states
of malignant cells across patients and within the same tumor. The intra-tumor transcriptional …

[HTML][HTML] Variant calling enhances the identification of cancer cells in single-cell RNA sequencing data

W Gasper, F Rossi, M Ligorio… - PLoS computational …, 2022 - journals.plos.org
Single-cell RNA-sequencing is an invaluable research tool that allows for the investigation
of gene expression in heterogeneous cancer cell populations in ways that bulk RNA-seq …

[PDF][PDF] CanSig: Discovering de novo shared transcriptional programs in single cancer cells

J Yates, F Barkmann, P Czyż, M Glettig, F Lohmann… - doi - academia.edu
Human tumors are highly heterogeneous in their cell composition; specifically, they exhibit
heterogeneity in transcriptional states of malignant cells, as has been recently discovered …

The contribution of uncharted RNA sequences to tumor identity in lung adenocarcinoma

Y Wang, H Xue, M Aglave, A Lainé, M Gallopin… - NAR …, 2022 - academic.oup.com
The identity of cancer cells is defined by the interplay between genetic, epigenetic
transcriptional and post-transcriptional variation. A lot of this variation is present in RNA-seq …

rcCAE: a convolutional autoencoder method for detecting intra-tumor heterogeneity and single-cell copy number alterations

Z Yu, F Liu, F Shi, F Du - Briefings in Bioinformatics, 2023 - academic.oup.com
Intra-tumor heterogeneity (ITH) is one of the major confounding factors that result in cancer
relapse, and deciphering ITH is essential for personalized therapy. Single-cell DNA …

KINOMO: A non-negative matrix factorization framework for recovering intra-and inter-tumoral heterogeneity from single-cell RNA-seq data

S Tagore, Y Wang, J Biermann, R Rabadan, E Azizi… - BioRxiv, 2022 - biorxiv.org
Single-cell RNA-sequencing (scRNA-seq) is a powerful technology to uncover cellular
heterogeneity in tumor ecosystems. Due to differences in underlying gene load, direct …

[HTML][HTML] Comprehensive discovery of subsample gene expression components by information explanation: therapeutic implications in cancer

S Pepke, G Ver Steeg - BMC medical genomics, 2017 - Springer
Background De novo inference of clinically relevant gene function relationships from tumor
RNA-seq remains a challenging task. Current methods typically either partition patient …

Inferring cancer progression from single-cell sequencing while allowing mutation losses

S Ciccolella, C Ricketts, M Soto Gomez… - …, 2021 - academic.oup.com
Motivation In recent years, the well-known Infinite Sites Assumption has been a fundamental
feature of computational methods devised for reconstructing tumor phylogenies and inferring …