- Location
-
Deutsche Nationalbibliothek Frankfurt am Main
- Extent
-
1 Online-Ressource.
- Language
-
Englisch
- Bibliographic citation
-
RNA splicing analysis using heterogeneous and large RNA-seq datasets ; volume:14 ; number:1 ; day:3 ; month:3 ; year:2023 ; pages:1-20 ; date:12.2023
Nature Communications ; 14, Heft 1 (3.3.2023), 1-20, 12.2023
- Creator
-
Vaquero-Garcia, Jorge
Aicher, Joseph K.
Jewell, San
Gazzara, Matthew R.
Radens, Caleb M.
Jha, Anupama
Norton, Scott S.
Lahens, Nicholas F.
Grant, Gregory R.
Barash, Yoseph
- Contributor
-
SpringerLink (Online service)
- DOI
-
10.1038/s41467-023-36585-y
- URN
-
urn:nbn:de:101:1-2024030108152907084805
- Rights
-
Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
-
14.08.2025, 10:56 AM CEST
Data provider
This object is provided by:
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Associated
- Vaquero-Garcia, Jorge
- Aicher, Joseph K.
- Jewell, San
- Gazzara, Matthew R.
- Radens, Caleb M.
- Jha, Anupama
- Norton, Scott S.
- Lahens, Nicholas F.
- Grant, Gregory R.
- Barash, Yoseph
- SpringerLink (Online service)
Other Objects (12)
An interpretable framework for clustering single-cell RNA-Seq datasets
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Detection of aberrant splicing events in RNA-seq data using FRASER
Context-based RNA-seq mapping
Genome-wide Determination Of Splicing Efficiency And Dynamics From RNA-Seq Data
KIS SPLICE: de-novo calling alternative splicing events from RNA-seq data
recount3: summaries and queries for large-scale RNA-seq expression and splicing
ASGAL: aligning RNA-Seq data to a splicing graph to detect novel alternative splicing events
Consequences and opportunities arising due to sparser single-cell RNA-seq datasets
Elimination of PCR duplicates in RNA-seq and small RNA-seq using unique molecular identifiers
SeqOthello: querying RNA-seq experiments at scale
An interpretable framework for clustering single-cell RNA-Seq datasets
GEMmaker: process massive RNA-seq datasets on heterogeneous computational infrastructure
SCRABBLE: single-cell RNA-seq imputation constrained by bulk RNA-seq data
Detection of aberrant splicing events in RNA-seq data using FRASER
Context-based RNA-seq mapping
Genome-wide Determination Of Splicing Efficiency And Dynamics From RNA-Seq Data
KIS SPLICE: de-novo calling alternative splicing events from RNA-seq data
recount3: summaries and queries for large-scale RNA-seq expression and splicing
ASGAL: aligning RNA-Seq data to a splicing graph to detect novel alternative splicing events
Consequences and opportunities arising due to sparser single-cell RNA-seq datasets
Elimination of PCR duplicates in RNA-seq and small RNA-seq using unique molecular identifiers
SeqOthello: querying RNA-seq experiments at scale
An interpretable framework for clustering single-cell RNA-Seq datasets
GEMmaker: process massive RNA-seq datasets on heterogeneous computational infrastructure
SCRABBLE: single-cell RNA-seq imputation constrained by bulk RNA-seq data
Detection of aberrant splicing events in RNA-seq data using FRASER
Context-based RNA-seq mapping
Genome-wide Determination Of Splicing Efficiency And Dynamics From RNA-Seq Data
KIS SPLICE: de-novo calling alternative splicing events from RNA-seq data
recount3: summaries and queries for large-scale RNA-seq expression and splicing
ASGAL: aligning RNA-Seq data to a splicing graph to detect novel alternative splicing events
Consequences and opportunities arising due to sparser single-cell RNA-seq datasets
Elimination of PCR duplicates in RNA-seq and small RNA-seq using unique molecular identifiers