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Reliable Identification of Genomic Variants from RNA-Seq Data
Identifying genomic variation is a crucial step for unraveling the relationship between genotype and phenotype and can yield important insights into human diseases. Prevailing methods rely on cost-intensive whole-genome sequencing (WGS) or whole-exome sequencing (WES) approaches while the identifica...
Tallennettuna:
| Päätekijät: | , , |
|---|---|
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
Elsevier
2013
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3791257/ https://ncbi.nlm.nih.gov/pubmed/24075185 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.ajhg.2013.08.008 |
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