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Admera Health
Admera Health is listed as a mid sized business research supplier in the Scientist.com network, with 3 sites in 1 country.
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Sites
3
Countries
1
Services
What this research supplier says it provides, as listed in the Scientist.com network.
Type of company: Mid sized business
Biomarkers
- Biomarker Clinical Utility Evaluate the potential clinical applications of a candidate biomarker.
- Biomarker Services Evaluating normal/abnormal biological conditions and characteristics within the body
- Epigenetics Epigenetics sits at the cutting edge of drug discovery. The ability to modify genomes without changing any sequences with methylation.
- Single Cell Transcriptome Sequencing Detect distinct, rare or abnomal cell types in a heterogenous population.
- Whole Transcriptome Amplification Amplify total RNA from a single cell.
Cell Culture and Characterization
- Single Cell DNA Sequencing Examine genetic variations in a single cell.
- Single Cell Services Request services to perform genomics, transcriptomics, proteomics, metabolomics and cell–cell interactions at the single cell level
Clinical Consulting
- Biomarker Services Consulting Expert advice to conduct solutions for evaluating normal/abnormal biological conditions and characteristics within the body.
Data Science/Bioinformatics
- In Silico Cancer Genomics/Cancer Transcriptomics Analysis Interpret DNA sequencing and microarray data for cancer studies.
DNA & RNA
- Amplicon - HLA Typing Use an amplicon sequencing method to identify allelic variation within the HLA genes.
- Amplicon 16s rRNA Sequencing Identify and compare bacteria present within a given sample.
- Bisulfite Sequencing (RRBS) Analyze genome-wide methylation profiles on a single nucleotide level.
- cDNA library construction Generate a library of recombinant cDNA clones.
- Cell Free DNA Assay Detect known mutations and discover new ones in cell-free plasma DNA.
- ChIP-Sequencing Use chromosome immunoprecipitation to identify DNA-protein binding sites in a genome.
Show all 50 in DNA & RNA
- ChIP-sequencing Profiling Identify where a protein is binding to DNA on a genome-wide scale.
- Cloning/Subcloning Clone or Subclone nucleotide sequence or gene.
- CRISPR Using advanced CRISPR technology, add or delete base pairs at a specifically targeted DNA loci.
- ddPCR-Based Plasma Genotyping Perform noninvasive tumor genotyping.
- De Novo Genome Sequencing Determine the DNA sequence of uncharacterized genomes.
- De Novo Transcriptome Sequencing Identify new genes without the need for a reference genome sequence.
- DNA Extraction Extract DNA from an original source.
- DNA Library Screening Screen genomic or cDNA libraries for positive clones.
- DNA Products Find DNA products including gDNA, cDNA clones, vectors and constructs from mice, insects, yeast, bacteria and viruses.
- DNA Sequencing Determine the nucleotide sequence of DNA samples.
- DNA/RNA Extraction & Purification DNA/RNA Extraction & Purification.
- Exome Sequencing Determine protein-coding nucleotide sequences in a DNA sample.
- Expression Profiling Measure the the expression of thousands of genes at once to create a global picture of cellular function.
- Genomic DNA Purification Isolate genomic DNA from cells or tissue samples.
- In Situ Hybridization Localize specific nucleic acid targets using labeled complementary probes.
- Long Read Sequencing Long read sequencing is used in genomics to sequence long fragments of DNA, enabling the ability to span complex regions of the genome.
- Metagenomic Sequencing Sequence genetic material recovered directly from environmental samples
- Methylation Analysis Determine genomic methylation patterns and analyze methylation in tumors and treated samples.
- miRNA sequencing Identify miRNAs by Next Generation Sequencing and bioinformatic analysis.
- mtDNA Sequencing Use next-generation sequencing (NGS) technology to detect and analyze mitochondrial mutations.
- Mutant Library Generate a library of variants of a single gene.
- NGS: Next Generation Sequencing Sequence millions of template DNA molecules in parallel.
- Nucleic Acid Hybridization Use a nucleic acid probe to identify complementary sequences.
- qPCR Analysis Measure the accumulation of PCR products in real time.
- Quantitative RT PCR Use quantitative reverse transcription polymerase chain reaction to measure absolute and relative mRNA abundance.
- RAD Sequencing Examine a small percentage of the target genome.
- RNA Amplification Produce RNA from pre-clinical and clinical samples for use in gene expression studies.
- RNA Extraction Isolate total RNA or mRNA from cells or tissues
- RNA Profiling Quantify the expression levels of mRNA transcripts, enabling the determination of gene expression patterns.
- RNA Sequencing Use Next Generation Sequencing techniques to Identify RNA transcripts, examine differential expression patterns and analyze splice variants.
- RNA Sequencing/Resequencing Identify RNA transcripts, examine differential expression patterns and analyze splice variants.
- Sanger Sequencing Sequence single strand DNA fragments using DNA Polymerase.
- Sequence Based Methylation Analysis Detect DNA methylation sites within cytosine-phosphate-guanine (CpG) dinucleotides at single base-pair resolution.
- Single Cell RNA Sequencing Quantify mRNA variants in a single cell.
- Single Molecule Real Time Sequencing Monitor the incorporation of fluorescently conjugated nucleotides within zero-mode waveguide (ZMW) chambers.
- SNP Characterization Identify single nucleotide polymorphisms to make genetic associations, analyze disease SNPs and determine LOH.
- Targeted Bisulphite Sequencing Reveal changes in DNA methylation associated with nuclear reprogramming.
- Targeted Sequencing/Resequencing Detect variations in a genome subset.
- TCR Repertoire Sequencing Analyze the T cell receptor repertoire by means of next-generation sequencing.
- Total RNA Sequencing Identify novel RNA transcripts and detect gene expression changes.
- Whole Genome Amplification (WGA) Amplify an entire genome from a single cell.
- Whole Genome Bisulphite Seq Profile genome-wide DNA methylation.
- Whole Genome Profiling Develop sequence-based physical maps for the assembly of genomes.
- Whole Genome Sequencing Determine the entire genetic make-up of an organism.
Show all 79 services
Human Biological Samples
- HBS Asthma For requesting HBS Asthma.
- HBS Leukemia For requesting HBS Leukemia
- Human Fecal Matter Acquire fresh/frozen normal feces based on patient demographics and history.
- Human Leukopaks Obtain enriched leukapheresis-derived products from normal peripheral blood.
- Human Plasma Acquire fresh/frozen human plasma
- Human Red Blood Cells Acquire fresh/frozen normal red blood cells based on patient demographics and history.
Show all 11 in Human Biological Samples
- Human Saliva Acquire fresh/frozen normal saliva based on patient demographics and history.
- Human Urine Acquire fresh/frozen normal urine based on patient demographics and history.
- Human Whole Blood Acquire fresh/frozen normal whole blood based on patient demographics and history.
- Multiple Sclerosis Human RNA Acquire fresh/frozen Multiple Sclerosis RNA based on patient demographics, disease stage, treatment and history.
- Stomach Cancer Human Fixed Tissue Acquire fixed Stomach Cancer tissue based on patient demographics, disease stage, treatment and history.
In Vitro Assays
- Assay Development Construct or create new assays or modify existing ones.
- ImmunoSEQ Assay Unmask the identity of millions of T- and B-cell receptors in a single sample using bias-controlled multiplex PCR amplification, high-throughput sequencing, and sophisticated bioinformatics.
In Vitro Pharmacology
- Drug Target Assays Gain insight into the selectivity and mode-of-action of a compound's pharmacological targets.
- Immuno-oncology Assays Use biochemical, cell based or in vivo assays to measure the activity of immuno-therapy targets.
Scientific Data Services
- Bioinformatics Bioinformatics is a powerful method of storing, retrieving and analyzing biological data.
- Epigenomics Data Analysis Quantify and analyze DNA methylation and/or DNA binding protein data sets.
- In Silico Metagenomics/Metatranscriptomics Data Analysis Use software to analyze genomic information from multiple environmental sources.
- Software Tools Software tool for statistical analysis, data mining, genome annotation or NGS data analysis.
Other services
- New Request
- Website
- www.admerahealth.com
Where it operates
Sites by country, with the cities in each.
-
United States 3 sites
Supplier diversity
SAM.gov small-business designations
Minority-owned
US small-business federal-contractor designation, self-certified in the U.S. federal System for Award Management (SAM.gov). Coverage is limited to matched U.S. small-business suppliers, so an absent designation is not evidence of its absence.
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