Manifest and cluster files used in Genome Studio analysis of Illumina arrays. Lists the Illumina-supplied manifest and cluster files for each array that were used in Genome Studio analysis. These files were downloaded from http://support.illumina.com/array/downloads.html . (DOCX 57 kb
Supplementary Tables. Table S1 lists the number of SNV and indel mutations found in each individual ...
Figure S4. Comparison of disk space usage between GenESysV and GEMINI. (TIFF 9492 kb
Taqman assays used for CNV assessment at 7 gene loci. Table S3. Cancer-predisposing genes disrupted ...
Overlap of CNV calls from two different algorithms for each array platform with gold standard and CN...
Gold standard and array CNV chromosomal coordinates. Spreadsheet 1 lists the chromosomal coordinates...
Cumulative frequencies of sizes of validated and non-validated CNV calls using platform specific alg...
Table S4. List of Copy Number Variation in Disease Database (CNVD). (XLSX 1074 kb
Table S3. List of Copy Number Variation in Clinvar Database. A collection of the Copy Number Variati...
Additional file 1. Table S1. The sample information of the natural population collected from dbVar a...
ARS library. Number of ARSs (y axis) for each coverage (x axis) in the ARS library, before transform...
Data further supporting the results including additional figures (Figures S1-S18) and tables (Tables...
General characteristics of the four subjects examined in the study. Table S2. Studied tissues and sa...
Table S2. Comparison of query performance between a single computer and a four-node cluster. (DOCX 9...
Full CNA data identified by array-CGH in the 50 Wilms tumor samples. CNA calling was performed using...
Supplementary Table S1. Correlation of PCNV findings from CMA and the QC array in 496 ES cases (DOCX...
Supplementary Tables. Table S1 lists the number of SNV and indel mutations found in each individual ...
Figure S4. Comparison of disk space usage between GenESysV and GEMINI. (TIFF 9492 kb
Taqman assays used for CNV assessment at 7 gene loci. Table S3. Cancer-predisposing genes disrupted ...
Overlap of CNV calls from two different algorithms for each array platform with gold standard and CN...
Gold standard and array CNV chromosomal coordinates. Spreadsheet 1 lists the chromosomal coordinates...
Cumulative frequencies of sizes of validated and non-validated CNV calls using platform specific alg...
Table S4. List of Copy Number Variation in Disease Database (CNVD). (XLSX 1074 kb
Table S3. List of Copy Number Variation in Clinvar Database. A collection of the Copy Number Variati...
Additional file 1. Table S1. The sample information of the natural population collected from dbVar a...
ARS library. Number of ARSs (y axis) for each coverage (x axis) in the ARS library, before transform...
Data further supporting the results including additional figures (Figures S1-S18) and tables (Tables...
General characteristics of the four subjects examined in the study. Table S2. Studied tissues and sa...
Table S2. Comparison of query performance between a single computer and a four-node cluster. (DOCX 9...
Full CNA data identified by array-CGH in the 50 Wilms tumor samples. CNA calling was performed using...
Supplementary Table S1. Correlation of PCNV findings from CMA and the QC array in 496 ES cases (DOCX...
Supplementary Tables. Table S1 lists the number of SNV and indel mutations found in each individual ...
Figure S4. Comparison of disk space usage between GenESysV and GEMINI. (TIFF 9492 kb
Taqman assays used for CNV assessment at 7 gene loci. Table S3. Cancer-predisposing genes disrupted ...