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path4204-sup-0001-Figure S1.docWord document50KFigure S1. Somatic SNV analysis of mucosal melanoma samples by whole exome sequencing: mutation spectrum and sequence context.
path4204-sup-0002-Table S1.docWord document41KTable S1. Number of mapped sequenced reads (in millions) and read lengths in the samples which underwent whole exome sequencing (WES) and whole genome sequencing (WGS).
path4204-sup-0003-Table S2.docWord document59KTable S2. Non-synonymous somatic SNVs detected by SomaticSniper exclusively in mucosal melanoma whole exome sequencing samples. Shown are the genomic coordinates and the gene for each variant.
path4204-sup-0004-Table S3.docWord document61KTable S3. Coding structural variants detected in mucosal melanoma sample K16404. Shown are the genomic coordinates for the left (Position 1) and right (Position 2) breakpoints. CTX = interchromosomal; ITX = intrachromosomal
path4204-sup-0005-Table S4.docWord document94KTable S4. Structural variants detected in mucosal melanoma sample K17842. Shown are the genomic coordinates for the left (Position 1) and right (Position 2) breakpoints. CTX = interchromosomal; ITX = intrachromosomal
path4204-sup-0006-Table S5.docWord document150KTable S5. Structural variants detected in mucosal melanoma sample M3. Shown are the genomic coordinates for the left (Position 1) and right (Position 2) breakpoints. CTX = interchromosomal; ITX = intrachromosomal.
path4204-sup-0007-Table S6.docWord document87KTable S6. Coding structural variants detected in mucosal melanoma sample N01803. Shown are the genomic coordinates for the left (Position 1) and right (Position 2) breakpoints. CTX = interchromosomal; ITX = intrachromosomal
path4204-sup-0008-Table S7.docWord document41KTable S7. Coding structural variants detected in mucosal melanoma sample N05408. Shown are the genomic coordinates for the left (Position 1) and right (Position 2) breakpoints. CTX = interchromosomal; ITX = intrachromosomal
path4204-sup-0009-Table S8.docWord document73KTable S8. nsSNVs detected by whole exome sequencing in mucosal melanoma sample N00101. Shown are the genomic coordinates and the gene for each variant
path4204-sup-0010-Table S9.docWord document57KTable S9. nsSNVs detected by whole exome sequencing in mucosal melanoma sample N01502. Shown are the genomic coordinates and the gene for each variant
path4204-sup-0011-Table S10.docWord document58KTable S10. nsSNVs detected by whole exome sequencing in mucosal melanoma sample M1. Shown are the genomic coordinates and the gene for each variant
path4204-sup-0012-Table S11.docWord document67KTable S11. nsSNVs detected by whole exome sequencing in mucosal melanoma sample N06610. Shown are the genomic coordinates and the gene for each variant
path4204-sup-0013-Table S12.docWord document170KTable S12. nsSNVs detected by whole exome sequencing in mucosal melanoma sample N10213. Shown are the genomic coordinates and the gene for each variant
path4204-sup-0014-Table S13.docWord document61KTable S13. nsSNVs detected by whole genome sequencing in mucosal melanoma sample N05408. Shown are the genomic coordinates and the gene for each variant
path4204-sup-0015-Table S14.docWord document77KTable S14. nsSNVs detected by whole genome sequencing in mucosal melanoma sample N01803. Shown are the genomic coordinates and the gene for each variant
path4204-sup-0016-Table S15.docWord document68KTable S15. nsSNVs detected by whole genome sequencing in mucosal melanoma sample M3. Shown are the genomic coordinates and the gene for each variant
path4204-sup-0017-Table S16.docWord document70KTable S16. nsSNVs detected by whole genome sequencing in mucosal melanoma sample K17842. Shown are the genomic coordinates and the gene for each variant
path4204-sup-0018-Table S17.docWord document123KTable S17. nsSNVs detected by whole genome sequencing in mucosal melanoma sample K16404. Shown are the genomic coordinates and the gene for each variant

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