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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...
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| Vydáno v: | Hum Genet |
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| Hlavní autoři: | , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
Springer Berlin Heidelberg
2017
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| Témata: | |
| On-line přístup: | 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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