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Comparing a few SNP calling algorithms using low-coverage sequencing data
BACKGROUND: Many Single Nucleotide Polymorphism (SNP) calling programs have been developed to identify Single Nucleotide Variations (SNVs) in next-generation sequencing (NGS) data. However, low sequencing coverage presents challenges to accurate SNV identification, especially in single-sample data....
Tallennettuna:
| Päätekijät: | , |
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| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
BioMed Central
2013
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3848615/ https://ncbi.nlm.nih.gov/pubmed/24044377 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1471-2105-14-274 |
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