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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...
Tallennettuna:
| Julkaisussa: | Hum Genet |
|---|---|
| Päätekijät: | , |
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
Springer Berlin Heidelberg
2017
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5418319/ https://ncbi.nlm.nih.gov/pubmed/28378101 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s00439-017-1788-5 |
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