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Clinical Epigenetics
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August 2, 2024
A case of an Angelman-syndrome caused by an intragenic duplication of UBE3A uncovered by adaptive nanopore sequencing
Laura Holthöfer, Stefan Diederich, Verena Haug, et al.
Nature Communications
|
March 31, 2026
Mapping human pre-rRNA processing and modification at single nucleotide resolution using long read nanopore sequencing
Stefan Pastore, Ludivine Wacheul, Lioba Lehmann, et al.
Nucleic Acids Research
|
July 19, 2025
ModiDeC: a multi-RNA modification classifier for direct nanopore sequencing
Nicolò Alagna, Stefan Mündnich, Johannes Miedema, et al.
Nucleic Acids Research
|
December 1, 2025
Direct RNA sequencing enables improved transcriptome assessment and tracking of RNA modifications for medical applications
Charlotte Hewel, Anna Wierczeiko, Johannes Miedema, et al.
Page
of 1
Search research articles
Search
Showing results (1-10 of 4) with videos related to
Sort By:
Page
of 1
Clinical Epigenetics
|
August 2, 2024
A case of an Angelman-syndrome caused by an intragenic duplication of UBE3A uncovered by adaptive nanopore sequencing
Laura Holthöfer, Stefan Diederich, Verena Haug, et al.
Nature Communications
|
March 31, 2026
Mapping human pre-rRNA processing and modification at single nucleotide resolution using long read nanopore sequencing
Stefan Pastore, Ludivine Wacheul, Lioba Lehmann, et al.
Nucleic Acids Research
|
July 19, 2025
ModiDeC: a multi-RNA modification classifier for direct nanopore sequencing
Nicolò Alagna, Stefan Mündnich, Johannes Miedema, et al.
Nucleic Acids Research
|
December 1, 2025
Direct RNA sequencing enables improved transcriptome assessment and tracking of RNA modifications for medical applications
Charlotte Hewel, Anna Wierczeiko, Johannes Miedema, et al.
Page
of 1