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Supplementary Figures S1-S25 from Late-stage metastatic melanoma emerges through a diversity of evolutionary pathways

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<p>Supplementary figure 1: Cohort overview. Number of samples sequenced with whole exome, panel or whole RNA sequencing. Supplementary figure 2: Phylogeny and WGD events in CRUKP1047. Supplementary figure 3: Ploidy and SCNA burden. Supplementary figure 4: Overview of each case. Supplementary figure 5: MEDICC2 copy number sample trees. Supplementary figure 6: MEDICC tree of all exome samples demonstrating that samples cluster together by patient, and not by melanoma subtype. Supplementary figure 7: SCNA frequency of cutaneous (a), acral (b) and melanoma of unknown primary (MUP, c). Supplementary figure 8: Correlation between liver copy number distance to other sites and time of emergence after stage IV diagnosis. Supplementary figure 9: Examination of tumour heterogeneity of alterations to antigen-presentation machinery genes,with site and patient annotation. Supplementary figure 10: Boxplots indicating the proportion of losses in the cohort for each segment. Supplementary figure 11: Balance of expression between nonsynonymous mutations that were not predicted to be neoantigens and clonal predicted neoantigens. Supplementary figure 12: Barplot of TIL infiltration score frequencies, determined by pathologist assessment of histology, across all samples. Supplementary figure 13: Number of samples per patient that are classified as either none-low in terms of TILs or moderate-heavy. Supplementary figure 14: Histogram of purity for samples with RNA-seq data. Supplementary figure 15: TME deconvolution. Supplementary figure 16: The effect of metastatic site on transcriptional profiles. Supplementary figure 17: Association of PHF3 copy number with expression. Supplementary figure 18: Overview of gene fusions identified in RNA-seq data. Supplementary figure 19: Comparison of ploidy estimates from panel sequencing data, exome data and FISH. Supplementary figure 20: Comparison of ploidy estimates in panel, exome, FISH and single cell data. Supplementary figure 21: FACs sort plot for CRUKP2567 diaphragmatic metastasis. Supplementary figure 22: Ploidy and wGII values from single cell sequencing of FACS-sorted tumour cells. Supplementary figure 23: Copy number profiles on chromosome 5 for bulk samples from primary and DI_2_R2, a diaphragmatic metastasis. Supplementary figure 24: Histogram of purity of samples for which RNA-seq was performed faceted by patient. Supplementary figure 25: Histogram of purity of samples for which RNA-seq was performed faceted by tissue site.</p>
Title: Supplementary Figures S1-S25 from Late-stage metastatic melanoma emerges through a diversity of evolutionary pathways
Description:
<p>Supplementary figure 1: Cohort overview.
Number of samples sequenced with whole exome, panel or whole RNA sequencing.
Supplementary figure 2: Phylogeny and WGD events in CRUKP1047.
Supplementary figure 3: Ploidy and SCNA burden.
Supplementary figure 4: Overview of each case.
Supplementary figure 5: MEDICC2 copy number sample trees.
Supplementary figure 6: MEDICC tree of all exome samples demonstrating that samples cluster together by patient, and not by melanoma subtype.
Supplementary figure 7: SCNA frequency of cutaneous (a), acral (b) and melanoma of unknown primary (MUP, c).
Supplementary figure 8: Correlation between liver copy number distance to other sites and time of emergence after stage IV diagnosis.
Supplementary figure 9: Examination of tumour heterogeneity of alterations to antigen-presentation machinery genes,with site and patient annotation.
Supplementary figure 10: Boxplots indicating the proportion of losses in the cohort for each segment.
Supplementary figure 11: Balance of expression between nonsynonymous mutations that were not predicted to be neoantigens and clonal predicted neoantigens.
Supplementary figure 12: Barplot of TIL infiltration score frequencies, determined by pathologist assessment of histology, across all samples.
Supplementary figure 13: Number of samples per patient that are classified as either none-low in terms of TILs or moderate-heavy.
Supplementary figure 14: Histogram of purity for samples with RNA-seq data.
Supplementary figure 15: TME deconvolution.
Supplementary figure 16: The effect of metastatic site on transcriptional profiles.
Supplementary figure 17: Association of PHF3 copy number with expression.
Supplementary figure 18: Overview of gene fusions identified in RNA-seq data.
Supplementary figure 19: Comparison of ploidy estimates from panel sequencing data, exome data and FISH.
Supplementary figure 20: Comparison of ploidy estimates in panel, exome, FISH and single cell data.
Supplementary figure 21: FACs sort plot for CRUKP2567 diaphragmatic metastasis.
Supplementary figure 22: Ploidy and wGII values from single cell sequencing of FACS-sorted tumour cells.
Supplementary figure 23: Copy number profiles on chromosome 5 for bulk samples from primary and DI_2_R2, a diaphragmatic metastasis.
Supplementary figure 24: Histogram of purity of samples for which RNA-seq was performed faceted by patient.
Supplementary figure 25: Histogram of purity of samples for which RNA-seq was performed faceted by tissue site.
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