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Figure 1 | BMC Genomics

Figure 1

From: Whole-exome sequencing of DNA from peripheral blood mononuclear cells (PBMC) and EBV-transformed lymphocytes from the same donor

Figure 1

Summary of the bioinformatic workflow followed. The raw sequence data was aligned to the hg19 human genome build (UCSC). Following the alignment of the sequence data, high-stringency parameters were used to make SNP and indel calls. Following the identification of genetic variants, the interpretation of our results included comparing the two-paired samples sequenced to determine if de novo mutations arise following EBV-transformation of B-lymphocytes.

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BMC Genomics

ISSN: 1471-2164

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