For each assembler we report the number of contigs/scaffolds produced (Ctg), the NG50, the percentage of short (Chaff) contigs (the percentage is computed with respect to the real genome length), the
The table provides a summary of the validation results, both for the INDELs common to the two sequencing datasets used, and the private ones. All INDELs sent for validation were classified as “novel”
Data from the 1000 genomes project (1KGP) and Complete Genomics (CG) have dramatically increased the numbers of known genetic variants and challenge several assumptions about the reference genome and
