| abstract |
The present invention relates to methods for identifying and/or quantifying low abundance, nucleotide base mutations, insertions, deletions, translocations, splice variants, miRNA variants, alternative transcripts, alternative start sites, alternative coding sequences, Methods of replacing non-coding sequences, alternative splicing, exon insertions, exon deletions, intron insertions, or other rearrangement and/or methylation of nucleotide bases at the genomic level. |