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Optimizing de novo assembly of short-read RNA-seq data for phylogenomics
BACKGROUND: RNA-seq has shown huge potential for phylogenomic inferences in non-model organisms. However, error, incompleteness, and redundant assembled transcripts for each gene in de novo assembly of short reads cause noise in analyses and a large amount of missing data in the aligned matrix. To a...
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| Hlavní autoři: | , |
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| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
BioMed Central
2013
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3663818/ https://ncbi.nlm.nih.gov/pubmed/23672450 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1471-2164-14-328 |
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