This file contains Supplementary Table S1, and provides the definition of copy number aberration states in CLImAT-HET. (PDF 104Â kb
Figure S1. The genome-wide copy number aberration frequency profile of the TCGA GBM dataset. (PDF 16...
List of genes selected for copy number validation of 9 focal rearrangements using real-time quantita...
Supplementary Tables. Table S1 lists the number of SNV and indel mutations found in each individual ...
The 207 tumor suppress genes (TSGs) with frequent copy number losses (CNLs). (XLSX 18 kb
Overview of single-cell sequencing samples and sequencing statistics. An overview of general sequenc...
The percentage of different mutational subtypes across all defined hotspot mutations. On each hotspo...
Full CNA data identified by array-CGH in the 50 Wilms tumor samples. CNA calling was performed using...
Figure S3. DNA copy number alterations in the IBC cohort. The genes with DNA copy number alterations...
Supplementary tables. Table S1. Cancer genes in detected amplification regions. Table S2. Cancer gen...
Algorithms S1-S3. Figures S1-S7. Table S4-S5, S7-S11. Supplementary materials. (PDF 1721 kb
Cohorts, ethnicity, and tumor stage of samples used for WES, SNP array, and qPCR. Table S2. Regions ...
Table S1. Genomic regions showing copy number loss or loss/LOH in at least 70% of ATM-associated tum...
Frequency of rs200757797 and rs2740090 in the 1000 Genomes continental groups. (DOCX 13.4 kb
Twenty mutation subtypes that were included in the statistical modeling of hotspot mutation definiti...
TCGA head and neck squamous cell carcinoma clinical information of tumors used in comparisons (nâ=...
Figure S1. The genome-wide copy number aberration frequency profile of the TCGA GBM dataset. (PDF 16...
List of genes selected for copy number validation of 9 focal rearrangements using real-time quantita...
Supplementary Tables. Table S1 lists the number of SNV and indel mutations found in each individual ...
The 207 tumor suppress genes (TSGs) with frequent copy number losses (CNLs). (XLSX 18 kb
Overview of single-cell sequencing samples and sequencing statistics. An overview of general sequenc...
The percentage of different mutational subtypes across all defined hotspot mutations. On each hotspo...
Full CNA data identified by array-CGH in the 50 Wilms tumor samples. CNA calling was performed using...
Figure S3. DNA copy number alterations in the IBC cohort. The genes with DNA copy number alterations...
Supplementary tables. Table S1. Cancer genes in detected amplification regions. Table S2. Cancer gen...
Algorithms S1-S3. Figures S1-S7. Table S4-S5, S7-S11. Supplementary materials. (PDF 1721 kb
Cohorts, ethnicity, and tumor stage of samples used for WES, SNP array, and qPCR. Table S2. Regions ...
Table S1. Genomic regions showing copy number loss or loss/LOH in at least 70% of ATM-associated tum...
Frequency of rs200757797 and rs2740090 in the 1000 Genomes continental groups. (DOCX 13.4 kb
Twenty mutation subtypes that were included in the statistical modeling of hotspot mutation definiti...
TCGA head and neck squamous cell carcinoma clinical information of tumors used in comparisons (nâ=...
Figure S1. The genome-wide copy number aberration frequency profile of the TCGA GBM dataset. (PDF 16...
List of genes selected for copy number validation of 9 focal rearrangements using real-time quantita...
Supplementary Tables. Table S1 lists the number of SNV and indel mutations found in each individual ...
DOI
Add to ORKG