| 摘要 |
An apparatus and method for generating a novel sequence in a target genome sequence for generating a novel sequence that does not exist in a reference sequence by using input reads that are not mapped to the reference sequence during genome re-sequencing of a next generation sequencing (NGS) technology. According to the present invention, the novel sequence that is not reflected to the reference sequence of the target genome sequence is generated, and information regarding the novel sequence may be provided. |
