Next Generation Sequencing (NGS) has the potential to unlock causative factors from our genetic material. NGS also represents a technological advancement using array-based sequencing that will improve many aspects of scientific research and advance the field of personalized medicine. Because of the sheer magnitude, precision and utilizable nature of the output data, a wealth of information will soon be available from studies completed using NGS. Avance Biosciences offers NGS with Illumina’s high throughput next generation sequencing platforms.
NGS is often done to accurately map genetic variants or mutations. Our genome variation analysis finds all high-confidence SNPs, indels, gene copy numbers, and genomic rearrangements from DNA-seq data. For non-model organisms, we produce annotated genome assemblies with computational post-processing steps to ensure the best possible starting point for future studies.
Genomics & Biological Services
All Avance Services Include
Experienced scientists functioning as project managers or study directors
Controlled laboratory environment to prevent cross-contamination
Rigorous sample tracking and handling procedures to prevent mistakes and cross-contamination
Methods validated per ICH GLP/GMP guidelines – also research grade testing available
Projects customized and tailored to suit your needs
Independent quality unit assuring regulatory compliance
Transparent process flow and weekly report on project progress
Professional project reports ready for regulatory filing
Fast turn-around time & Competitive pricing