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Human Y chromosome copy number variation in the next generation sequencing era and beyond
The human Y chromosome provides a fertile ground for structural rearrangements owing to its haploidy and high content of repeated sequences. The methodologies used for copy number variation (CNV) studies have developed over the years. Low-throughput techniques based on direct observation of rearrang...
| Autores principales: | , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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Springer Berlin Heidelberg
2017
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5418319/ https://www.ncbi.nlm.nih.gov/pubmed/28378101 http://dx.doi.org/10.1007/s00439-017-1788-5 |