e9bc1b7fbc3372c180b67365be9b4da442e87971
Supplemental_Methods_and_Results.md
| ... | ... | @@ -16,8 +16,8 @@ Any study that described at least one gene as recurrently mutated in DLBCL, FL o |
| 16 | 16 | 15 studies for FL,[@barariaCathepsinAlterationsInduce2020; @cheungAcquiredTNFRSF14Mutations2010; @drevalGeneticSubdivisionsFollicular2023; @hubschmannMutationalMechanismsShaping2021; @krysiakRecurrentSomaticMutations2017; @laurentFollicularLymphomaComprises2024; @louissaintPediatrictypeNodalFollicular2016; @maSubtypespecificCooccurringGenetic2022; @morinFrequentMutationHistonemodifying2011; @morinSomaticMutationsAltering2010; @okosunRecurrentMTORC1activatingRRAGC2016; @pasqualucciInactivatingMutationsAcetyltransferase2011; @rossiAberrantSomaticHypermutation2006; @russler-germainMutationsAssociatedProgression2023; @yildizActivatingSTAT6Mutations2015] and 13 studies for BL.[@abateDistinctViralMutational2015; @burkhardtClinicalRelevanceMolecular2022; @grandeGenomewideDiscoverySomatic2019; @johnstonCmycHypermutationBurkitt1992; @loveGeneticLandscapeMutations2012; @maSubtypespecificCooccurringGenetic2022; @muppidiLossSignalingGa132014; @paneaWholeGenomeLandscape2019; @richterRecurrentMutationID32012; @schmitzBurkittLymphomaPathogenesis2012; @thomasGeneticSubgroupsInform2023; @wildaInactivationARFMDM2p53Pathway2004; @zhouSporadicEndemicBurkitt2019] The number of Tier 1, 2 and 3 genes originating from each of these studies is summarized below. |
| 17 | 17 | |
| 18 | 18 | <figure> |
| 19 | -<img src="" alt="flags1" style="width:500px;"/> |
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| 20 | -<figcaption><strong>Supplemental Figure S1. Comparing FLAGS rank in the DLBCL genes.</strong> <br> |
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| 19 | +<img src="DLBCL_FL_BL_sankey_all-1.svg" alt="flags1" style="width:500px;"/> |
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| 20 | +<figcaption><strong>Supplemental Figure S1. The originating studies for all DLBCL, FL and BL genes.</strong> <br> |
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| 21 | 21 | The FLAGS rank of DLBCL genes in Tier 1, 2 and 3 is compared. The genes in the COSMIC CGC list are included for comparison. Values closer to 1 indicate the gene has a higher number of rare germline variants. |
| 22 | 22 | </figcaption> |
| 23 | 23 | </figure> |