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A robust framework for detecting structural variations in a genome
Motivation: Recently, structural genomic variants have come to the forefront as a significant source of variation in the human population, but the identification of these variants in a large genome remains a challenge. The complete sequencing of a human individual is prohibitive at current costs, wh...
| Autores principales: | , , |
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| Formato: | Texto |
| Lenguaje: | English |
| Publicado: |
Oxford University Press
2008
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2718654/ https://www.ncbi.nlm.nih.gov/pubmed/18586745 http://dx.doi.org/10.1093/bioinformatics/btn176 |