Cargando…
Validation of Splicing Events in Transcriptome Sequencing Data
Genomic alignments of sequenced cellular messenger RNA contain gapped alignments which are interpreted as consequence of intron removal. The resulting gap-sites, genomic locations of alignment gaps, are landmarks representing potential splice-sites. As alignment algorithms report gap-sites with a co...
Autores principales: | Kaisers, Wolfgang, Ptok, Johannes, Schwender, Holger, Schaal, Heiner |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2017
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5485934/ https://www.ncbi.nlm.nih.gov/pubmed/28545234 http://dx.doi.org/10.3390/ijms18061110 |
Ejemplares similares
-
Sample Size Estimation for Detection of Splicing Events in Transcriptome Sequencing Data
por: Kaisers, Wolfgang, et al.
Publicado: (2017) -
Hierarchical Clustering of DNA k-mer Counts in RNAseq Fastq Files Identifies Sample Heterogeneities
por: Kaisers , Wolfgang, et al.
Publicado: (2018) -
Ranking noncanonical 5′ splice site usage by genome-wide RNA-seq analysis and splicing reporter assays
por: Erkelenz, Steffen, et al.
Publicado: (2018) -
Succession of splicing regulatory elements determines cryptic 5΄ss functionality
por: Brillen, Anna-Lena, et al.
Publicado: (2017) -
Age, gender and UV-exposition related effects on gene expression in in vivo aged short term cultivated human dermal fibroblasts
por: Kaisers, Wolfgang, et al.
Publicado: (2017)