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Inocras
Inocras is listed as a small business research supplier in the Scientist.com network, with 2 sites in 1 country.
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Sites
2
Countries
1
Services
What this research supplier says it provides, as listed in the Scientist.com network.
Type of company: Small business
Antibodies
- Antibody Sequencing Sequence cDNA encoding variable heavy (VH) and variable light (VL) domains of a hybridoma cell line.
Biomarkers
- Biomarker Clinical Utility Evaluate the potential clinical applications of a candidate biomarker.
- Biomarker Discovery Identify a biomarker associated with disease progression of disease, effectiveness of therapy or diagnosis of disease or condition.
- Diagnostic Biomarkers Discovery Identify candidate biomarkers indicative of the presence of a disorder.
- Epigenetics Epigenetics sits at the cutting edge of drug discovery. The ability to modify genomes without changing any sequences with methylation.
- Pharmacodynamic Biomarkers Discovery Identify candidate biomarkers indicative of the therapeutic outcome of a drug-target interaction.
- Predictive Biomarkers Discovery Identify candidate biomarkers suggestive of a response to a treatment.
Show all 9 in Biomarkers
- Prognostic Biomarkers Discovery Identify candidate biomarkers representative of disease progression without treatment.
- Single Cell Transcriptome Sequencing Detect distinct, rare or abnomal cell types in a heterogenous population.
- Solid Tumor CDx Design and validate companion diagnostics for solid tumors that help select the most appropriate patients, identify patients at increased risk, or monitor treatment effectiveness.
Cell Culture and Characterization
- Microsatellite Instability Analysis Compare allelic profiles and detect genomic instability.
- Single Cell DNA Sequencing Examine genetic variations in a single cell.
Clinical Trials
- Clinical Trial Design Develop study-related protocols, case report forms (CRFs) and database tools for records management.
- Patient Recruitment Recruit and retain patients for clinical trials.
Companion Diagnostics
- Cervical Cancer CDx Design and validate companion diagnostics for cervical cancer that help select the most appropriate patients, identify patients at increased risk, or monitor treatment effectiveness.
- Pancreatic Cancer CDx Design and validate companion diagnostics for pancreatic cancer that help select the most appropriate patients, identify patients at increased risk, or monitor treatment effectiveness.
Show all 56 services
Data Science/Bioinformatics
- Clinical Trial Integration Analysis The process of combining data from multiple clinical trials to understand categories of drugs and drug behavior in a more global way.
- Discovery In Silico Genomics/Transcriptomics Data Analysis A process that helps make sense of your Genomics/Transcriptomics data
DNA & RNA
- Bisulfite Seq DNA Methylation Analysis Determine DNA methylation status at single-base resolution
- Bisulfite Sequencing (RRBS) Analyze genome-wide methylation profiles on a single nucleotide level.
- Cell Free DNA Assay Detect known mutations and discover new ones in cell-free plasma DNA.
- De Novo Genome Sequencing Determine the DNA sequence of uncharacterized genomes.
- DNA Extraction Extract DNA from an original source.
- DNA Sequencing Determine the nucleotide sequence of DNA samples.
Show all 28 in DNA & RNA
- 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.
- Genotyping Examine a DNA sequence to identify specific genetic varients .
- Integrated Genomics Package Process an entire Genomics Pipeline Project including: Sample Preparation, Target Enrichment, NGS Instrumentation, and Data Analysis from our Bundle of Suppliers
- Methylation Analysis Determine genomic methylation patterns and analyze methylation in tumors and treated samples.
- mtDNA Sequencing Use next-generation sequencing (NGS) technology to detect and analyze mitochondrial mutations.
- NGS: Next Generation Sequencing Sequence millions of template DNA molecules in parallel.
- Non-Bisulfite DNA Methylation Analysis Analyze DNA methylation by methods such as differential enzymatic cleavage or affinity capture
- 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.
- RNAseq and DNAseq library preparation and sequencing DNA/RNA sequencing and preparations
- 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.
- Targeted Sequencing/Resequencing Detect variations in a genome subset.
- 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.
Human Biological Samples
- Human DNA Acquire human DNA.
- Human DNA & RNA Acquire fresh/frozen Human DNA & RNA based on patient demographics, disease stage, treatment and history
- Liquid Biopsy Test and detect either circulating tumor cell-associated biomarkers or circulating tumor DNA.
In Vitro Assays
- Assay Development Construct or create new assays or modify existing ones.
In Vitro Pharmacology
- High Throughput Screening Conduct millions of chemical, genetic or pharmacological tests in a short period of time.
Real World Evidence & Data
- RWD - Genomics Genomic data collected from a patients with different diseases, can be derived from a range of sources.
Scientific Data Services
- Cancer Systems Biology Convert complex molecular data obtained from high-throughput technologies to deducible information.
- Epigenomics Data Analysis Quantify and analyze DNA methylation and/or DNA binding protein data sets.
- Genome Data Analysis Analyze genomic DNA, RNA and protein sequence data.
- NGS: Next Generation Sequencing Data Analysis Use software to interpret data created by RNA-Seq, DNA-Seq, ChIP-Seq and DNA methylation experiments.
- Website
- inocras.com
Where it operates
Sites by country, with the cities in each.
-
United States 2 sites
Work with Inocras on Scientist.com
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