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Genseq
Genseq 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
Agricultural Sciences Research & Development
- Molecular Markers Use of molecular diagnostics to analyze biological markers in the genome and proteome.
Biomarkers
- Biomarker Analytical Validation Assess and optimize the characteristics of a candidate biomarker to ensure reproducibility and consistency.
- Biomarker Clinical Utility Evaluate the potential clinical applications of a candidate biomarker.
- Biomarker Clinical Validation Evaluate the predictive ability of a candidate biomarker for a disorder.
- Biomarker Discovery Identify a biomarker associated with disease progression of disease, effectiveness of therapy or diagnosis of disease or condition.
- Biomarker Services Evaluating normal/abnormal biological conditions and characteristics within the body
- Diagnostic Biomarkers Discovery Identify candidate biomarkers indicative of the presence of a disorder.
Show all 14 in Biomarkers
- Multi-Omics Study Use an integrated multi-omics study to understand a disease mechanism.
- 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.
- Prognostic Biomarkers Discovery Identify candidate biomarkers representative of disease progression without treatment.
- Single Cell quantitative Real Time-PCR Assess gene expression levels and patterns in a single cell.
- 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.
- Whole Transcriptome Amplification Amplify total RNA from a single cell.
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.
- Single Cell Services Request services to perform genomics, transcriptomics, proteomics, metabolomics and cell–cell interactions at the single cell level
Clinical Trials
- Phase 1-3 Studies Design phase 1-3 studies that seek to identify if a drug is safe, effective, and more efficient than other available treatments on the market.
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 104 services
Data Science/Bioinformatics
- Clinical Biomarker Analysis An approach to finding markers that change in response to a drug or that identify a group that responds favorably to a specific therapy. These can be omics, molecular, histologic, radiologic, etc.
- Clinical Companion Diagnostics Analysis The process of finding patients who are likely to respond positively to a drug and designing a diagnostic tool to identify this group of patients before or with a therapy.
- Clinical Data Analysis Analysis that helps you make sense of your clinical data
- Clinical In Silico Genomics/Transcriptomics Data Analysis A process that helps make sense of your omics data
- Clinical Responder Analysis, Patient Stratification The process of identifying patients that are more likely to respond positively to a drug.
- Discovery Bioinformatics Different analytical approaches that make, store, and analyze complex biological data.
Show all 17 in Data Science/Bioinformatics
- Discovery Biomarker Analytics An approach to finding markers that change in response to a drug or that identify a group that responds favorably to a specific therapy. These can be omics, molecular, histologic, radiologic, etc.
- Discovery Data Analysis Analysis that helps you make sense of your discovery data
- Discovery Data Science and Modeling A process that helps make sense of your discovery data
- Discovery In Silico Genomics/Transcriptomics Data Analysis A process that helps make sense of your Genomics/Transcriptomics data
- Discovery Omics Analytics A process to analyze various omics data (genomics, transcriptomics, proteomics, metabolomics, etc.) This can include the integration of different omics data. Helps to better understand the molecular environment...
- Microarray Data Analysis Visualize and analyze microarray data and facilitate data analysis for large experiments.
- Microsatellite Analysis for Normal Tumor Instability (MANTIS) Classify samples by MSI status utilizing NGS data.
- Translational Bioinformatics Different analytical approaches that make, store, and analyze complex biological data.
- Translational Biomarker Discovery An approach to finding markers that change in response to a drug or that identify a group that responds favorably to a specific therapy. These can be omics, molecular, histologic, radiologic, etc.
- Translational In Silico Genomics/Transcriptomics Data Analysis A process that helps make sense of your omics data
- Translational Omics Analytics A process to analyze various omics data (genomics, transcriptomics, proteomics, metabolomics, etc.) This can include the integration of different omics data. Helps to better understand the molecular environment...
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.
- De Novo Transcriptome Sequencing Identify new genes without the need for a reference genome sequence.
- DNA Extraction Extract DNA from an original source.
Show all 46 in DNA & RNA
- DNA Library Screening Screen genomic or cDNA libraries for positive clones.
- DNA Sequencing Determine the nucleotide sequence of DNA samples.
- DNA Synthesis Produce DNA fragments for microarrays, PCR, cloning and expression studies.
- 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.
- Gene/Oligo Synthesis Synthesize oligonucleotide or gene for microarrays, RT-PCR and PCR cloning.
- 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
- 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.
- Methylation Analysis Determine genomic methylation patterns and analyze methylation in tumors and treated samples.
- Methylation Specific PCR Determine the methylation status of a CpG site without the need for base-specific endonucleases.
- 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.
- NGS: Next Generation Sequencing Sequence millions of template DNA molecules in parallel.
- Poly (A) tail Length Profiling (PAL-Seq) Conduct high-throughput sequencing of individual mRNA poly (A) tails.
- 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.
- RNA Services Whether you’re isolating total RNA for whole genome expression analysis by microarray or setting up high content screening by s...
- RNAseq and DNAseq library preparation and sequencing DNA/RNA sequencing and preparations
- 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.
- SNP Characterization Identify single nucleotide polymorphisms to make genetic associations, analyze disease SNPs and determine LOH.
- Spatial Transcriptomics Determine the sub-cellular localization of mRNA molecules. Use this to identify cellular heterogeneity in tissues, tumors, immune cells and the subcellular distribution of transcripts.
- Target Gene Expression Measure expression of a target gene at the protein, RNA and DNA level.
- Targeted Sequencing/Resequencing Detect variations in a genome subset.
- TCR Repertoire Sequencing Analyze the T cell receptor repertoire by means of next-generation sequencing.
- Tissue Microarray Screen large numbers of tissues for the presence or absence of specific molecular markers.
- 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 Sequencing Determine the entire genetic make-up of an organism.
Drug Development
- Bioinformatics Consulting Consulting Services for the science of collecting and analyzing complex biological data
- Pharmacogenetics Consulting Access genomic services required for clinical trials, such as genotyping, genetic variation testing and DNA isolation.
Lab Supplies, Facilities, and Equipment
- Biobanking Store and track biological samples.
Oncology Models
- Hematological Cancer PDX Design and validate companion diagnostics for hematological cancer that help select the most appropriate patients, identify patients at increased risk, or monitor treatment effectiveness.
- Oncology Models Use model organisms to test the therapeutic efficacy of cancer drug candidates.
Pharmacovigilance
- GxP Compliance Monitoring Ensure products or services adhere to a set minimum standard.
Primary Market Research
- GDPR, HIPAA, BHBIA, EphMRA Compliance Ensures compliance with data privacy, ethical, and regional marketing research regulations. Mitigates legal risk and builds trust with participants and clients.
- In-depth interviews (IDIs) One-on-one qualitative interviews conducted with key stakeholders to explore beliefs, decision drivers, and unmet needs. Delivers rich narrative data to inform trial design, product positioning, and message development.
Real World Evidence & Data
- RWD - Oncology Data from oncology patients, can include clinical treatment, diagnosis, among others.
- RWD - Rare Diseases Data from patients with rare diseases, can include clinical treatment, diagnosis, among others.
Scientific Data Services
- Bioinformatics Bioinformatics is a powerful method of storing, retrieving and analyzing biological data.
- Cancer Systems Biology Convert complex molecular data obtained from high-throughput technologies to deducible information.
- Genome Data Analysis Analyze genomic DNA, RNA and protein sequence data.
- Marker Analyses Identify associations between genetic markers and traits of interest to determine markers responsible for human diseases.
- Mutation Data Profiling Guide treatment decisions in cancer based on the identification of genomic mutations .
- NGS: Next Generation Sequencing Data Analysis Use software to interpret data created by RNA-Seq, DNA-Seq, ChIP-Seq and DNA methylation experiments.
Show all 9 in Scientific Data Services
- Pharmaco-genomics Genetic polymorphism contribution to inter-individual variability in drugs' responses and/or adverse events.
- Small RNA Gene Expression Quantify and analyze miRNA, piRNA, siRNA as well as other small nuclear RNAs from small-RNA-seq raw input data sets.
- Software Tools Software tool for statistical analysis, data mining, genome annotation or NGS data analysis.
Other services
- New Request
- Website
- www.genseqgroup.com
Where it operates
Sites by country, with the cities in each.
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Ireland 2 sites
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