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A Long-Read Sequencing Approach for Direct Haplotype Phasing in Clinical Settings
The reconstruction of individual haplotypes can facilitate the interpretation of disease risks; however, high costs and technical challenges still hinder their assessment in clinical settings. Second-generation sequencing is the gold standard for variant discovery but, due to the production of short...
Wedi'i Gadw mewn:
| Cyhoeddwyd yn: | Int J Mol Sci |
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| Prif Awduron: | , , , , , , , |
| Fformat: | Artigo |
| Iaith: | Inglês |
| Cyhoeddwyd: |
MDPI
2020
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| Pynciau: | |
| Mynediad Ar-lein: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7731377/ https://ncbi.nlm.nih.gov/pubmed/33271988 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/ijms21239177 |
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