Fig. 1From: Discovery of large genomic inversions using long range informationSequence signatures used by the Valor algorithm. In the presence of an inverted haplotype in the sequenced genome, we look for both read pair and split clone signatures. Paired-end reads that span the inversion breakpoints will be mapped to the same strand with a large distance between them, instead of the concordant read pairs that map to opposing strands [1, 20]. Large insert clones will show mapping properties similar to the split read sequence signature [36], but since we do not have the full clone sequence, or sufficient coverage to assemble clones, we interrogate lengths of contiguous read mapping (Methods)Back to article page