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XEGEN

XEGEN is listed as a small consultant research supplier in the Scientist.com network, with 1 site in 1 country.

Search companies, drugs, suppliers and investigators, and follow each one to the others. Individual plan, $249/seat/mo. Card required.

Sites 1

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Type of company: Small consultant

Antibodies

Hybridoma Sequencing/Antibody Sequencing Determine the sequences of monoclonal antibodies.

Biomarkers

Multi-Omics Study Use an integrated multi-omics study to understand a disease mechanism.
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

Chemical and Compound Analysis

Amino Acid Analysis (AAA) Determine protein quantities, relative compositions and amino acid content profiles.

Chemistry, Manufacturing and Controls (CMC)

Targeted Locus Amplification (TLA) Technology This technology enables targeted complete sequencing of any locus of interest.

Clinical Consulting

Biostatistics Consulting Apply statistical theory and mathematical principals to research
Clinical Trial Consulting Consulting services for Clinical trials.

Data Science/Bioinformatics

Biostatistical Design Use statistics to ensure appropriate pre-clinical and clinical study design.
Discovery Statistical and Mathematical Modeling Use mathematical variables and equations to establish relationships between data.
In Silico Cancer Genomics/Cancer Transcriptomics Analysis Interpret DNA sequencing and microarray data for cancer studies.
In Silico Epigenetic Compound Library Screening Use computer-aided methods to discover new compounds against key regulators of epigenetic signaling.
In Silico Nucleic Acid Microarray Analysis Use software to visualize and evaluate gene activity in response to various stimuli.
In Silico Protein Microarray Analysis Use software to visualize and evaluate protein function and expression on a large scale.

Show all 81 services 65 more

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.
Amplified Fragment Length Polymorphism Detection Detect DNA polymorphisms based upon restriction enzyme digestion and PCR.
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.
ChIP-Sequencing Use chromosome immunoprecipitation to identify DNA-protein binding sites in a genome.

Show all 51 in DNA & RNA 45 more

ChIP-sequencing Profiling Identify where a protein is binding to DNA on a genome-wide scale.
Chromatin Interaction Analysis-Paired End Tag Sequencing Sequence DNA using Chromatin Conformation Capture (3C) together with Chromatin Immunoprecipitation (ChIP).
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.
Degradome Sequencing Use parallel analysis of RNA ends (PARE) to detect miRNA targets and analyze patterns of RNA degradation.
DNA Hydroxy Methylation Seq Use epigenetic services to analyze genome-wide DNA hydroxymethylation.
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-lipid interaction analysis Investigate cellular dynamics based on changes in fluorescent properties.
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.
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
Metagenomic Sequencing Sequence genetic material recovered directly from environmental samples
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.
Non-Bisulfite DNA Methylation Analysis Analyze DNA methylation by methods such as differential enzymatic cleavage or affinity capture
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.
Ribosome Profiling Determine which mRNAs are being actively translated using next generation sequencing and specialized messenger RNA (mRNA)
RNA Interference Use small sequences of RNA that correspond to the targeted gene product to inhibit mRNA translation.
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...
RNAscope In Situ Assays Profile single-cell gene expression in situ.
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.
Target Gene Expression Measure expression of a target gene at the protein, RNA and DNA level.
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.
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

General Marketing

Database Management Software Facilitate the collection, tracking and processing of biological facts, statistics and observations.

Protein Sciences

N-terminal Sequencing Determine the amino acid sequence of an intact protein from its N-terminus.

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

Bioinformatics Bioinformatics is a powerful method of storing, retrieving and analyzing biological data.
Discovery Computational Systems Biology Model the interaction of biological system with drug candidates.
Epigenomics Data Analysis Quantify and analyze DNA methylation and/or DNA binding protein data sets.
In Silico Genomics/Transcriptomics Data Analysis Interpret DNA sequencing and microarray data.
In Silico Metagenomics/Metatranscriptomics Data Analysis Use software to analyze genomic information from multiple environmental sources.
Marker Analyses Identify associations between genetic markers and traits of interest to determine markers responsible for human diseases.

Show all 10 in Scientific Data Services 4 more

Metagenomics Data Analysis Deconvolute the genetic content of genomes contained in environmental samples by utilizing whole genome sequencing techniques to provide insight into microbial communities and host phenotypes.
Mutation Data Profiling Guide treatment decisions in cancer based on the identification of genomic mutations .
Pharmaco-genomics Genetic polymorphism contribution to inter-individual variability in drugs' responses and/or adverse events.
Software Tools Software tool for statistical analysis, data mining, genome annotation or NGS data analysis.

Website: xegen.fr

France Gémenos 1 site

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