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High-resolution detection of chromosomal rearrangements in leukemias through mate pair whole genome sequencing
The detection of recurrent somatic chromosomal rearrangements is standard of care for most leukemia types. Even though karyotype analysis—a low-resolution genome-wide chromosome analysis—is still the gold standard, it often needs to be complemented with other methods to increase resolution. To evalu...
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| Vydáno v: | PLoS One |
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| Hlavní autoři: | , , , , , , , , , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
Public Library of Science
2018
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5846771/ https://ncbi.nlm.nih.gov/pubmed/29529047 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0193928 |
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