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Towards accurate detection and genotyping of expressed variants from whole transcriptome sequencing data
BACKGROUND: Massively parallel transcriptome sequencing (RNA-Seq) is becoming the method of choice for studying functional effects of genetic variability and establishing causal relationships between genetic variants and disease. However, RNA-Seq poses new technical and computational challenges comp...
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| Main Authors: | , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BioMed Central
2012
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3394419/ https://ncbi.nlm.nih.gov/pubmed/22537301 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1471-2164-13-S2-S6 |
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