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Characterizing complex structural variation in germline and somatic genomes
Genome structural variation (SV) is a major source of genetic diversity in mammals and a hallmark of cancer. While SV is typically defined by its canonical forms – duplication, deletion, insertion, inversion and translocation – recent breakpoint mapping studies have revealed a surprising number of “...
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| Main Authors: | , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2011
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| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3249479/ https://ncbi.nlm.nih.gov/pubmed/22094265 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.tig.2011.10.002 |
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