A universal algorithm for de novo decrypting of heterozygous indel sequences: A tool for personalized medicine

This algorithm is unique amongst all the existing algorithms in terms of performing the task of indel detection, size determination, and decrypting simultaneously. This universal approach eliminates the requirement of a reference sequence or sequence tracing and makes this algorithm unique in decrypting unprecedented sequenced genomes. Because of the high frequency of heterozygous indels in human genome, this universal algorithm will greatly reduce the time required for post-sequencing data analysis in whole genome sequencing of an individual for the practice of personalized medicine.