Figure 1From: ParMap, an algorithm for the identification of small genomic insertions and deletions in nextgen sequencing dataParMap employs reads that are partially mapped to a reference genome to identify genomic variations. These variations include small insertions and deletions of less than 10 nucleotides. When the sequenced read (line 2) is mapped to the reference genome (line 1), the unmatched bases are marked as gaps (line 3), adjacent to position p (Methods).Back to article page