Rapid detection of myeloid neoplasm fusions using single-molecule long-read sequencing.
Recurrent gene fusions are common drivers of disease pathophysiology in leukemias. Identifying these structural variants helps stratify disease by risk and assists with therapy choice. Precise molecular diagnosis in low-and-middle-income countries (LMIC) is challenging given the complexity of assays...
| Päätekijät: | , , , , , , , |
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| Aineistotyyppi: | Artikkeli |
| Kieli: | English |
| Julkaistu: |
Public Library of Science (PLoS)
2023-01-01
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| Sarja: | PLOS Global Public Health |
| Linkit: | https://doi.org/10.1371/journal.pgph.0002267 |