Associated Papers
Next-Generation Sequencing-Based Genomic Profiling of Children with Acute Myeloid Leukemia.
Krizsán S et al.
The Journal of Molecular Diagnostics : Jmd, 2023
37088137 (PubMed )
Supplement: mmc4.xlsx › Supplementary_Table_S4
DeteX: A highly accurate software for detecting SNV and InDel in single and paired NGS data in cancer research.
Cui Y et al.
Frontiers in Genetics, 2022
36685970 (PubMed )
Supplement: Table4.xlsx › Sheet1
hgvs: A Python package for manipulating sequence variants using HGVS nomenclature: 2018 Update.
Wang M et al.
Human Mutation, 2018
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