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Optimized Next-Generation Sequencing Genotype-Haplotype Calling for Genome Variability Analysis
The accurate estimation of nucleotide variability using next-generation sequencing data is challenged by the high number of sequencing errors produced by new sequencing technologies, especially for nonmodel species, where reference sequences may not be available and the read depth may be low due to...
Tallennettuna:
| Julkaisussa: | Evol Bioinform Online |
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| Päätekijät: | , , , , |
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
SAGE Publications
2017
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5582667/ https://ncbi.nlm.nih.gov/pubmed/28894353 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1177/1176934317723884 |
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