Next-Gen Applications
Whole-Genome DeNovo Sequencing
Through a multi-platform approach, a scaffold of your genome is created using the long reads and positional information of the Titanium™ paired-end chemistries. Next, coverage is built up using SOLiD™ V3's high throughput. Finally, Sanger sequencing is used to close any remaining gaps.
Metagenomic Sequencing
Utilizing the long reads of the 454 GS-FLX Titanium system, SeqWright provides reliable metagenomic sequencing services which enable you to efficiently identify nearly all of the microbes present within your environmental samples.
CHiP Sequencing
Leveraging SOLiD 3 and 454 Titanium, SeqWright provides genome-wide digital ChIP-seq services which rapidly identify bound transcription factors and other proteins throughout your genome of interest.
Small RNA Discovery and Profiling
The massive throughput and hundreds of milliions of reads SOLiD™ 3 generates are ideal for profiling known small RNA molecules as well as discovering novel ones.
Whole-Transcriptome Sequencing
The flexibility of both the SOLiD™ and Titanium™ Platforms, with their ability to analyze DNA and RNA, allow for reliable transcriptome analysis for ANY organism for which a reference sequence exists.
Structural Variation Analysis
The positional information provided by SOLiD™ mate-pair or Titanium™ paired-end libraries enable genome-wide scanning for INDELs, Duplications, Rearrangements, and Chromosomal breakpoints.
Deep Resequencing
The accuracy of SOLiD's™ dual-base encoding chemistry make it a powerful tool for resequencing projects. With throughput up to 6GB, we can provide ultra deep re-sequencing coverage and confident SNP detection.
And more... |
