VBiolabs

Illumina Sequencing
VBiolabs leverages the power of Illumina/Solexa Genome Analyzer II to meet  the most demanding sequencing requirements. The Genome analyser is based on massively parallel sequencing of millions of fragments using reversible terminator-based sequencing chemistry. This sequencing technology offers a robust high throughput sequencing system that meets the need for productivity, cost-effectiveness and accuracy among next-generation sequencing technologies.

Illumina Sequencing technology operates with relatively short read lengths (~50 bp/read) thus is specifically suitable for short RNA research applications. In addition, this technology allows 80-100 million reading clusters to be sequenced in one experiment, providing researchers with the capability for whole genome sequencing.

Applications

Genome resequencing
BAC resequencing
Expression profiling
Small RNA identification
ChIP sequencing
Paired ends sequencing

 

Variation analysis:

Microsatellite analysis
Amplified fragment length polymorphism (AFLP)
Loss of heterozygosity (LOH)
Single strand conformation polymorphism (SSCP)

Transcriptome analysis

Serial Analysis of Gene Expression (SAGE) sequencing
Full-length cDNA analyses
Noncoding RNA Sequencing

Technical features

Read-length: up to 50 bp/read
Number of reads/run: 80 million reads/run
Samples/run: 8 channels (1 flowcell)
 
 

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