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Fig. 3 | BMC Genomics

Fig. 3

From: Unexpected effects of different genetic backgrounds on identification of genomic rearrangements via whole-genome next generation sequencing

Fig. 3

Candidate SV calls detected in samples of different genetic backgrounds before any filtering process. Top: the number of total SVs including DELs (deletions), CTXs (inter-chromosomal translocations) and others (see details in Additional file 2: Figure S1). Bottom: the number of CTXs in 10 sequenced samples including 6 tumor samples (119J, 125J, 196J, 202J, 46J, and 90J) and 4 control samples (control 1, control 2, kidney and wt B6) plus 129S1 whose sequences were downloaded from Sanger’s Institute (see details in Methods)

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