Additional file 3: Table S3. of Genome-wide segregation of single nucleotide and structural variants into single cancer cells

Cell Capture Metrics. This file provides an overview of the number of cells captured and included in the analyses after surpassing quality control criteria, as well as. (PDF 21 kb

Additional file 2: Table S2. of Genome-wide segregation of single nucleotide and structural variants into single cancer cells

List of Somatic Single-Nucleotide Variants Identified in this Sample. This file provides a list of single-nucleotide variants confirmed in the bulk patient sample, as well as the location and number of supporting reads output by VarScan. (XLSX 48 kb

Additional file 4: Table S4. of Genome-wide segregation of single nucleotide and structural variants into single cancer cells

List of Amplicon Primers used in Resequencing. This file provides a list of the primers used for interrogating the bulk and single cell samples for single-nucleotide and structural variants. (XLSX 57 kb

Additional file 1: Table S1. of Genome-wide segregation of single nucleotide and structural variants into single cancer cells

List of Somatic Structural Variants Identified in this Sample. This file provides a list of structural variants confirmed in the bulk patient sample, as well as the location, quality, and breakpoint sequence data output by CREST. (XLSX 52 kb