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Evaluating the effect of reference genome divergence on the analysis of empirical RADseq datasets
The advent of high‐throughput sequencing (HTS) has made genomic‐level analyses feasible for nonmodel organisms. A critical step of many HTS pipelines involves aligning reads to a reference genome to identify variants. Despite recent initiatives, only a fraction of species has publically available re...
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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John Wiley and Sons Inc.
2020
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7391306/ https://www.ncbi.nlm.nih.gov/pubmed/32760550 http://dx.doi.org/10.1002/ece3.6483 |