The Other Custom Library for High-Throughput Sequencer
□ Our Servies
High-throughput sequencer, also known as next-generation sequencing (NGS), has revolutionized genomic research. In recent years, NGS technology has steadily improved, with costs dropping, providing researchers a wide rang of applications.
In addition to the unique libraries based on our original technologies, DNAFORM also provides flexible library preparation service.
DNAFORM constructs a library for genome sequence according to the applications.
- □Whole genome sequence
A library for optimized for whole-genome sequencing. Genome-wide variation analysis is one of its major applications.
- □De-novo sequence
De novo genome sequencing is used to sequence uncharacterized genomes where there is no reference sequence available, or known genomes where significant structural variation is expected.
- □Target resequencing
Targeted resequencing involves isolation of genomic regions of interest in a sample library, that typically investigate a few (or few dozen) genes to detect germline and somatic variants across large populations.
Combining chromatin immunoprecipitation (ChIP) with massively parallel DNA sequencing, ChIP-Seq allows genome-wide identification of the DNA-associated protein binding sites, It is the effective technique to investigate genomic region involved in gene regulation or chromatin organization.
- □Directional RNA-Seq
- □Non-directional RNA-Seq
RNA-Seq is utilized for quantitative investigation of transcripts and their structure. Non-directional provides information on sequence data of a novel transcript, as well as novel splice variant. Moreover, non-direct RNA-Seq allows detection of anti-sense RNAs that was not available by the directional RNA-Seq.
Small RNA-Seq is utilized for the discovery and profiling of microRNAs and other non-coding RNA on any organism.