Changes in isoform variants and relative abundancies are an important clue in deciphering how genomic variants drive the phenotypic differences between health and disease. Only long-read sequencing can provide unbiased, direct detection of all the isoforms present in the samples.
Iso-sequencing analysis allows us to generate full length cDNA sequences without assembly. It characterizes transcript isoforms within targeted genes or across an entire transcriptome.
For more information and quotation, kindly contact us at NGS@biobasic-asia.com