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iMapSplice: Alleviating reference bias through personalized RNA-seq alignment
Genomic variants in both coding and non-coding sequences can have functionally important and sometimes deleterious effects on exon splicing of gene transcripts. For transcriptome profiling using RNA-seq, the accurate alignment of reads across exon junctions is a critical step. Existing algorithms th...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6086400/ https://www.ncbi.nlm.nih.gov/pubmed/30096157 http://dx.doi.org/10.1371/journal.pone.0201554 |