Accessing and Analysis of the Human Genome has Never Been Easier
- CLIA certified.
- Scalable to any size of project.
- Fast turnaround times.
- High quality and accurate results.
- FASTQ files 40X.
- BAM and VCF files subject to validation and deliverable specs.
- Personalized medicine and pharmacogenomics.
- Genetic disease screening.
- Tumor analysis.
Neogen® Genomics has been a leader in the innovation of WHGS, which offers the most detailed view into our genetic code. WHGS can evaluate every base in the genome and navigate the complexity of genomic variants that make us unique. Previously a challenging application, human whole-genome sequencing is now one of the simplest. Advances in library preparation, sequencing, bioinformatics, and variant analysis have made it possible to go from sample to report in less than 30 hours.
Contact genomicsinfo@Neogen.com or call 877.443.6489 for more information.