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Performance of High-Throughput Sequencing for the Discovery of Genetic Variation Across the Complete Size Spectrum
We observed that current high-throughput sequencing approaches only detected a fraction of the full size-spectrum of insertions, deletions, and copy number variants compared with a previously published, Sanger-sequenced human genome. The sensitivity for detection was the lowest in the 100- to 10,000...
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| Päätekijät: | , , , , |
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| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
Genetics Society of America
2013
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3887540/ https://ncbi.nlm.nih.gov/pubmed/24192839 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1534/g3.113.008797 |
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