Searching journal content for articles similar to Pacholewska et al. 34 (11): 1832.

Displaying results 1-2 of 2

For checked items

view abstracts
download to citation manager

Select this article
Method: Single-cell Rapid Capture Hybridization sequencing reliably detects isoform usage and coding mutations in targeted genes
- Hongke Peng,
- Jafar S. Jabbari,
- Luyi Tian,
- Changqing Wang,
- Yupei You,
- Chong Chyn Chua,
- Natasha S. Anstee,
- Noorul Amin,
- Andrew H. Wei,
- Nadia M. Davidson,
- Andrew W. Roberts,
- David C.S. Huang,
- Matthew E. Ritchie,
- and Rachel Thijssen
Genome Res. April 2025 35: 942-955; Published in Advance January 10, 2025, doi:10.1101/gr.279322.124
...-read single-cell RNA sequencing (scRNA-seq) data reveals significant gene expression differences in SF3B1-mutated CLL cells, although it does not impact the sensitivity of the anticancer drug venetoclax. scRaCH-seq's capability to study long-read transcripts of multiple genes makes it a powerful tool...
OPEN ACCESS ARTICLE
Select this article
Editorial: Revolutionizing genomics and medicine—one long molecule at a time
- Ana Conesa,
- Alexander Hoischen,
- and Fritz J. Sedlazeck
Genome Res. November 2024 34: ix-xi; doi:10.1101/gr.280179.124
..., Königs A, Heß F, Becker K, Köhrer K, Kaiser J, et al. 2024. Long-read transcriptome sequencing of CLL and MDS patients uncovers molecular effects of SF3B1 mutations. Genome Res (this issue) 34: 1832–1848. doi:10.1101/gr.279327.124 ↵Ritter AJ, Draper JM, Vollmers C, Sanford JR. 2024. Long-read subcellular...

For checked items

view abstracts
download to citation manager

Modify Results

Citation format:
Results / page:
Results order:

Preprint Server

Current Issue

March 2026, 36 (3)