ADVANCING TODAY FOR A HEALTHIER TOMORROW

In the fight against disease, our NGS solutions provide the valuable insights needed to advance non-clinical healthcare research.  From sequencing a few genes, to the whole exome, to the whole genome, Rapid Genomics provides total NGS solutions focused on high-quality, cost-effective data.

 

WHOLE-GENOME SEQUENCING (WGS)

WGS scans the entire genome for the comprehensive discovery of genetic mutations, structural variants, and copy number variants with a single assay. Rapid Genomics can adjust the sequencing depth to meet research goals and project requirements.

Any sample volume

Tunable sequencing depth

Flexible data reporting

  • FASTQ files
  • Single-nucleotide polymorphisms (SNPs)

Custom data analysis

  • QTL & SNP association mapping
  • Functional gene identification
  • Translational research

CAPTURE-SEQ: EXOME SEQUENCING

Exome sequencing provides efficient, targeted sequencing results to investigate disease, rare disorders, cancer, or population studies. Capture-Seq is more cost-effective than WGS in targeting protein coding regions, without limiting detection range of rare variants.

Any sample volume

Tunable sequencing depth

Multiple exome panels available

  • Agilent Sureselect
  • Roche Nimblegen
  • Illumina® TruSeq DNA Exome
  • Customized panels

Custom data analysis

  • Variant detection & association