Associated Papers
Clinical Validation of Whole Genome Sequencing for Cancer Diagnostics.
Roepman P et al.
The Journal of Molecular Diagnostics : Jmd, 2021
ClinVAP: a reporting strategy from variants to therapeutic options.
Sürün B et al.
Bioinformatics (oxford, England), 2020
31830259 (PubMed )
Supplement: btz924_supplementary_data.zip › btz924-suppl_data › SupplementaryMaterialB_ExampleReport.pdf
Exome sequencing identifies recurrent mutations of the splicing factor SF3B1 gene in chronic lymphocytic leukemia.
Quesada V et al.
Nature Genetics, 2011
Somatic SF3B1 mutation in myelodysplasia with ring sideroblasts.
Papaemmanuil E et al.
The New England Journal of Medicine, 2011
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