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Identifying potential germline variants from sequencing hematopoietic malignancies
Next-generation sequencing (NGS) of bone marrow and peripheral blood increasingly guides clinical care in hematological malignancies. NGS data may help to identify single nucleotide variants, insertions/deletions, copy number variations, and translocations at a single time point, and repeated NGS te...
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| Vydáno v: | Hematology Am Soc Hematol Educ Program |
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| Hlavní autoři: | , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
American Society of Hematology
2020
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7727528/ https://ncbi.nlm.nih.gov/pubmed/33275754 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1182/hematology.2020006910 |
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