Searching journal content for articles similar to Mitsutomi et al. 35 (11): 2406.

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  1. Research: Genetic regulation of nascent RNA maturation revealed by direct RNA nanopore sequencing
    • Karine Choquet,
    • Louis-Philippe Chaumont,
    • Simon Bache,
    • Autum R. Baxter-Koenigs,
    • and L. Stirling Churchman
    Genome Res. April 2025 35: 712-724; Published in Advance February 14, 2025, doi:10.1101/gr.279203.124
    ...the many introns of a human gene are removed can substantially influence AS, while nascent RNA polyadenylation can affect RNA stability and decay. However, how splicing order and poly(A) tail length are regulated by genetic variation has never been explored. Here, we used direct RNA nanopore sequencing...
  2. Method: Rapid and accurate demultiplexing of direct RNA nanopore sequencing data with SeqTagger
    • Leszek P. Pryszcz,
    • Gregor Diensthuber,
    • Laia Llovera,
    • Rebeca Medina,
    • Anna Delgado-Tejedor,
    • Luca Cozzuto,
    • Julia Ponomarenko,
    • and Eva Maria Novoa
    Genome Res. April 2025 35: 956-966; Published in Advance January 29, 2025, doi:10.1101/gr.279290.124
    ...assembly and decoding of molecular tags with DNA-based nanopore signatures. Nat Commun 11: 5454. doi:10.1038/s41467-020-19151-8 ↵Drexler HL, Choquet K, Churchman LS. 2020. Splicing kinetics and coordination revealed by direct nascent RNA sequencing through nanopores. Mol Cell 77: 985–998.e8. doi:10.1016/j...
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  3. Method: An optimized protocol for quality control of gene therapy vectors using nanopore direct RNA sequencing
    • Kathleen Zeglinski,
    • Christian Montellese,
    • Matthew E. Ritchie,
    • Monther Alhamdoosh,
    • Cédric Vonarburg,
    • Rory Bowden,
    • Monika Jordi,
    • Quentin Gouil,
    • Florian Aeschimann,
    • and Arthur Hsu
    Genome Res. November 2024 34: 1966-1975; Published in Advance October 28, 2024, doi:10.1101/gr.279405.124
    ...of cryptic poly(A) sites. Similarly, for PacBio sequencing, the lower number of reads and high cost per base limited the identification of rarer splicing events.ONT direct RNA sequencing identifies cryptic poly(A) and splice sitesTo further evaluate the utility of nanopore direct RNA sequencing for LV QC, we...
  4. Method: Long-read RNA sequencing reveals allele-specific N6-methyladenosine modifications
    • Dayea Park and
    • Can Cenik
    Genome Res. April 2025 35: 999-1011; Published in Advance October 29, 2024, doi:10.1101/gr.279270.124
    ...). Five micrograms of total RNA without poly(A) RNA isolation was used for DRS (Viscardi and Arribere 2022). The library was generated using the Oxford Nanopore Direct RNA Sequencing Kit (Nanopore SQK-RNA002) following the manufacturer's protocol. The RNA sequencing from each RNA replicate was performed...
  5. Method: Detecting m6A RNA modification from nanopore sequencing using a semisupervised learning framework
    • Haotian Teng,
    • Marcus Stoiber,
    • Ziv Bar-Joseph,
    • and Carl Kingsford
    Genome Res. November 2024 34: 1987-1999; Published in Advance October 15, 2024, doi:10.1101/gr.278960.124
    ...Intyre et al. 2020; Zhang et al. 2021), low single-nucleotide resolutions (Dominissini et al. 2012; Meyer et al. 2012), and, importantly, an inability to identify the exact location of a modification.Direct RNA sequencing using nanopores offers a promising alternative (Garalde et al. 2018). An RNA molecule...
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  6. Method: Deep structural clustering reveals hidden systematic biases in RNA sequencing data
    • Qiang Su,
    • Yi Long,
    • Deming Gou,
    • Junmin Quan,
    • Xiaoming Zhou,
    • and Qizhou Lian
    Genome Res. November 2025 35: 2563-2577; Published in Advance September 19, 2025, doi:10.1101/gr.280713.125
    ...-in sequences reveals 16 major clusters among the 65,536 spike-ins. (D,E) Visualization of all spike-in RNAs, color-coded by GC-content cluster and by MFE cluster. The nine GC-content categories and 120 MFE levels reflect the full breadth of the 65,536 spike-in sequences.For validation, we designed synthetic...
  7. Method: PoreMeth2 for decoding the evolution of methylome alterations with nanopore sequencing
    • Gianluca Mattei,
    • Marta Baragli,
    • Barbara Gega,
    • Alessandra Mingrino,
    • Martina Chieca,
    • Tommaso Ducci,
    • Gianmaria Frigè,
    • Luca Mazzarella,
    • Romina D'Aurizio,
    • Francesco De Logu,
    • Romina Nassini,
    • Pier Giuseppe Pelicci,
    • and Alberto Magi
    Genome Res. November 2025 35: 2501-2512; Published in Advance October 20, 2025, doi:10.1101/gr.280259.124
    ...with Salmon v. 0.14.1 and the reference transcriptome GRCh37 from Ensembl. Normalization and statistical analysis were performed with DESeq2 (v. 1.30.1). DEGs with adjusted P-value < 0.05, as scored by the Benjamin–Hopkins formula, and absolute log2FC > 0.5 were selected. DNA and RNA nanopore sequencing data...
  8. Research: Enhanced detection of RNA modifications and read mapping with high-accuracy nanopore RNA basecalling models
    • Gregor Diensthuber,
    • Leszek P. Pryszcz,
    • Laia Llovera,
    • Morghan C. Lucas,
    • Anna Delgado-Tejedor,
    • Sonia Cruciani,
    • Jean-Yves Roignant,
    • Oguzhan Begik,
    • and Eva Maria Novoa
    Genome Res. November 2024 34: 1865-1877; Published in Advance September 13, 2024, doi:10.1101/gr.278849.123
    ...contributed equally to this work. Corresponding authors: oguzhan.begik@crg.eu, eva.novoa@crg.euAbstractIn recent years, nanopore direct RNA sequencing (DRS) became a valuable tool for studying the epitranscriptome, owing to its ability to detect multiple modifications within the same full-length native RNA...
  9. Research: Assessing the readiness of Oxford Nanopore sequencing for clinical genomics applications
    • Judith Arres,
    • Santosh Elavalli,
    • Shalini Behl,
    • Daniel Matias Sanchez,
    • Ayesha Al Ali,
    • Abdelrahman Ahmed Yehia Abdelaziz Saad,
    • Azza Attia,
    • Cyla Minas,
    • Sharika Pariyachery,
    • Shariq Ahmed,
    • Fatmah Aldhuhoori,
    • Nitu Thulasidharan,
    • Gurunath Katagi,
    • Omar Soliman,
    • Shilp Purohit,
    • Vinay Kusuma,
    • Raony Cardenas,
    • Thyago Cardoso,
    • Luis F. Paulin,
    • Philippe Sanio,
    • Joseph Mafofo,
    • Haiguo Wu,
    • Val Zvereff,
    • Albarah El-Khani,
    • Fahed Al Marzooqi,
    • Tiago R. Magalhães,
    • Fritz J. Sedlazeck,
    • and Javier Quilez
    Genome Res. March 2026 36: 460-471; Published in Advance February 11, 2026, doi:10.1101/gr.280134.124
    ...: jquilez@m42.aeAbstractLong-read sequencing (LRS) technologies, namely, Oxford Nanopore Technologies (ONT) and Pacific Biosciences (PacBio), have emerged as promising solutions to overcome the limitations of short-read sequencing (SRS). Nevertheless, the still higher sequencing error rates compared...
  10. Research: Long-read sequencing reveals HBV integration patterns and oncogenic impact on early-onset hepatocellular carcinoma
    • Yao Wang,
    • Dong Yu,
    • Yue Mei,
    • ZhiDa Fu,
    • Jian Lin,
    • Di Wu,
    • Yuan Yang,
    • and Hongli Yan
    Genome Res. November 2025 35: 2389-2405; Published in Advance September 16, 2025, doi:10.1101/gr.279889.124
    ...committee of Changhai Hospital. Written consent was obtained from the patients. The clinicopathological information of the patients is listed in Supplemental Table S1.DNA and RNA extractionHigh-molecular-weight (HMW) gDNA and total RNA were extracted from fresh-frozen tumor and matched nontumor tissues...
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