Use the speed and scale of NGS to advance your genomic studies
Genomics
NGS Genomics Services
Whole Genome Sequencing
Discover Single Nucleotide Polymorphisms (SNPs), Copy Number Variation (CNV), and Structural Variation.
Flexible sample type, including FFPE curls or slides, blood, saliva, etc.
Scalable high throughput capability operating in CLIA-lab
Bioinformatic support including QC, Mapping, Markdup, BQSR, Germline Variant Analysis, and more
Epigenomics
Evaluate methylation sites with our comprehensive epigenomic services.
Whole Genome Bisulfite Sequencing (WGBS) and RRBS evaluate DNA methylation sites; ChIP-seq and ATAC-seq inform on accessible areas of chromatin that relate to epigenomic mapping, patterns of epigenetic markers, aberrant methylation characteristics of cancers, and much more.
16s rRNA sequencing
Admera Health’s 16s rRNA-SEQ™ is a proprietary assay that improves upon current techniques.
Lower bias with higher sensitivity and specificity
Detects bacterial and archaeal genera at a broader range
ITS sequencing
Identify fungal species through ITS1 and ITS2 amplification.
Fast turnaround for those studying environmental diversity
Expert bioinformatic support
Metagenomics
Metagenomics offers a powerful lens for viewing the microbial world that has the potential to revolutionize understanding of the entire living world.
Extraction from a variety of sample types including environmental samples
Industry leading turnaround time
Flexible sample input
Shotgun sequencing
Amplicon-seq
Sequencing of targeted amplicons with high quality data output.
CRISPR screening with technical and project support
Automated workflow for high sample volume and data throughput
Custom Panels
Customized solutions for specific targets (e.g. CRISPR screening). Our team of experts will tailor to your specifications.
xGen® target capture products
TruSeq Custom Amplicon Low Input
Agilent Sureselect Custom Bait
CRISPR screening with technical and project support
Whole Exome Sequencing
Most disease-related variants are found in exons, exome sequencing is a method to understand genetic causes of diseases or conditions.
Optimized workflow for FFPE samples
Expert scientific and project support
IDT, SureSelect, Twist Biosciences, Illumina capture options
Mature bioinformatics pipelines
Advantages of Working with Admera Health
Industry Leading
Turnaround Time
Admera Health operates with urgency to deliver data while maintaining industry-leading quality
Flexible Sample Types
Admera Health has optimized workflows to support ultra-low input with challenging samples
Custom Depth of Coverage
Admera Health offers high throughput capabilities to accommodate custom coverages
