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State of the art de novo assembly of human genomes from massively parallel sequencing data
Recent studies in human genomes have demonstrated the use of de novo assemblies to identify genetic variations that are difficult for mapping-based approaches. Construction of multiple human genome assemblies is enabled by massively parallel sequencing, but a conventional bioinformatics solution is...
Gorde:
| Egile Nagusiak: | , , , |
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| Formatua: | Artigo |
| Hizkuntza: | Inglês |
| Argitaratua: |
BioMed Central
2010
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| Gaiak: | |
| Sarrera elektronikoa: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3525208/ https://ncbi.nlm.nih.gov/pubmed/20511140 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1479-7364-4-4-271 |
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