Table S1 - Comparison of Sequencing Platforms for Single Nucleotide Variant Calls in a Human Sample

The putative allele, the flanking sequence in the genome, PCR and extension primers used in this study are listed in this spreadsheet. The sheet “Only 454” lists the details for locations that were only called using 454 generated sequences, “Only Illumina” refers to the details for locations that were only called by sequences generated using Illumina HiSeq 2000 sequencing, and “Only SOLiD” refers to the details for the locations that were only called by sequences generated using SOLiD 3 ECC technology. “454 and Illumina”, “454 and SOLiD”, and “Illumina and SOLiD” refer to details for locations that were called by only two of the three sequencing platforms that were used in this study. (XLSX)