Recent advances in cancer fusion transcript detection

R Dorney, BP Dhungel, JEJ Rasko… - Briefings in …, 2023 - academic.oup.com
Extensive investigation of gene fusions in cancer has led to the discovery of novel
biomarkers and therapeutic targets. To date, most studies have neglected chromosomal …

The peptide woods are lovely, dark and deep: Hunting for novel cancer antigens

D Oreper, S Klaeger, S Jhunjhunwala… - Seminars in …, 2023 - Elsevier
Harnessing the patient's immune system to control a tumor is a proven avenue for cancer
therapy. T cell therapies as well as therapeutic vaccines, which target specific antigens of …

Accurate detection of tumor-specific gene fusions reveals strongly immunogenic personal neo-antigens

D Weber, J Ibn-Salem, P Sorn, M Suchan… - Nature …, 2022 - nature.com
Cancer-associated gene fusions are a potential source for highly immunogenic
neoantigens, but the lack of computational tools for accurate, sensitive identification of …

nextNEOpi: a comprehensive pipeline for computational neoantigen prediction

D Rieder, G Fotakis, M Ausserhofer, G Rene… - …, 2022 - academic.oup.com
Somatic mutations and gene fusions can produce immunogenic neoantigens mediating
anticancer immune responses. However, their computational prediction from sequencing …

Fast and sensitive validation of fusion transcripts in whole-genome sequencing data

V Hafstað, J Häkkinen, H Persson - BMC bioinformatics, 2023 - Springer
Background In cancer, genomic rearrangements can create fusion genes that either
combine protein-coding sequences from two different partner genes or place one gene …

Proteogenomic analysis reveals non-small cell lung cancer subtypes predicting chromosome instability, and tumor microenvironment

KJ Song, S Choi, K Kim, HS Hwang, E Chang… - Nature …, 2024 - nature.com
Non-small cell lung cancer (NSCLC) is histologically classified into lung adenocarcinoma
(LUAD) and lung squamous cell carcinoma (LSCC). However, some tumors are …

Insights into mechanisms of pheochromocytomas and paragangliomas driven by known or new genetic drivers

SK Flores, CM Estrada-Zuniga, K Thallapureddy… - Cancers, 2021 - mdpi.com
Simple Summary Pheochromocytomas and paragangliomas are rare neuroendocrine
tumors that are often hereditary. Although research has advanced considerably, significant …

PolyASite v3. 0: a multi-species atlas of polyadenylation sites inferred from single-cell RNA-sequencing data

Y Moon, CJ Herrmann, A Mironov… - Nucleic Acids …, 2024 - academic.oup.com
The broadly used 10X Genomics technology for single-cell RNA sequencing (scRNA-seq)
captures RNA 3′ ends. Thus, some reads contain part of the non-templated polyadenosine …

Clinical interpretation of whole-genome and whole-transcriptome sequencing for precision oncology

V Jobanputra, KO Wrzeszczynski, R Buttner… - Seminars in Cancer …, 2022 - Elsevier
Whole-genome sequencing either alone or in combination with whole-transcriptome
sequencing has started to be used to analyze clinical tumor samples to improve diagnosis …

Whole-Genome and Transcriptome Sequencing-Based Characterization of Bacillus Cereus NR1 From Subtropical Marine Mangrove and Its Potential Role in Sulfur …

M Kashif, Z Lu, Y Sang, B Yan, SJ Shah… - Frontiers in …, 2022 - frontiersin.org
Sulfur, organosulfur compounds, and sulfides are essential parts of life. Microbial sulfate
assimilation is among the most active and ancient metabolic activities in the sulfur cycle that …