Genomix4Life
Genomix4Life is an innovative SME specializing in functional genomics and bioinformatics. It offers services in life sciences with bioinformatic and project support, utilizing advanced high-throughput technologies for research and validation of biomarkers, genome and exome analysis, transcriptomics, non-coding RNA, and microbiota. The company is committed to advancing scientific and health research through personalized genomics and bioinformatics solutions.
Industries
Nr. of Employees
small (1-50)
Genomix4Life
Via Salvatore Allende, 84084 Fisciano SA, Italy
Products
Next Generation Sequencing (NGS)
Provides high-throughput sequencing services using platforms like Illumina HiSeq2500, NextSeq 500, MiSeq, and Ion Torrent PGM for applications such as whole genome sequencing, targeted re-sequencing, RNA sequencing, metagenomics, and epigenomics.
Bioinformatics Analysis
Offers bioinformatics services including data analysis, interpretation, and storage to support genomic research and clinical applications.
Microarray Services
Provides microarray-based DNA genotyping and gene expression analysis using platforms like Illumina BeadXpress and iScan.
Biomarker Discovery
Focuses on identifying and characterizing biomarkers for early disease detection, particularly in cancer, to guide therapy choices and monitor disease progression.
Nucleic Acids Isolation
Offers DNA and RNA extraction services to prepare samples for sequencing and other genomic analyses.
Quality Controls
Performs quality control of nucleic acids using instruments like Nanodrop 2000c, Agilent 2100 Bioanalyzer, Agilent 4200 TapeStation, and Qubit 2.0 Fluorometer to ensure sample integrity for sequencing and microarray applications.
Next Generation Sequencing (NGS)
Provides high-throughput sequencing services using platforms like Illumina HiSeq2500, NextSeq 500, MiSeq, and Ion Torrent PGM for applications such as whole genome sequencing, targeted re-sequencing, RNA sequencing, metagenomics, and epigenomics.
Bioinformatics Analysis
Offers bioinformatics services including data analysis, interpretation, and storage to support genomic research and clinical applications.
Microarray Services
Provides microarray-based DNA genotyping and gene expression analysis using platforms like Illumina BeadXpress and iScan.
Biomarker Discovery
Focuses on identifying and characterizing biomarkers for early disease detection, particularly in cancer, to guide therapy choices and monitor disease progression.
Nucleic Acids Isolation
Offers DNA and RNA extraction services to prepare samples for sequencing and other genomic analyses.
Quality Controls
Performs quality control of nucleic acids using instruments like Nanodrop 2000c, Agilent 2100 Bioanalyzer, Agilent 4200 TapeStation, and Qubit 2.0 Fluorometer to ensure sample integrity for sequencing and microarray applications.
Services
Provision of high-throughput sequencing for whole genomes, exomes and targeted panels; sample processing and raw data delivery.
Custom computational analysis of sequencing and omics data, pipeline development and interpretation for research projects.
Single-cell library preparation and analysis for cellular-resolution transcriptomic studies.
Microarray assays and high-throughput omics services including transcriptomics and small RNA analysis.
NGS-based forensic profiling workflows for degraded samples, phenotype prediction, ancestry inference and kinship analyses.
Research support for biomarker identification and validation using high-throughput genomic methods.
Provision of high-throughput sequencing for whole genomes, exomes and targeted panels; sample processing and raw data delivery.
Custom computational analysis of sequencing and omics data, pipeline development and interpretation for research projects.
Single-cell library preparation and analysis for cellular-resolution transcriptomic studies.
Microarray assays and high-throughput omics services including transcriptomics and small RNA analysis.
NGS-based forensic profiling workflows for degraded samples, phenotype prediction, ancestry inference and kinship analyses.
Research support for biomarker identification and validation using high-throughput genomic methods.
Expertise Areas
- Functional genomics
- Next-generation sequencing services
- Bioinformatics and computational analysis
- Single-cell genomics
Key Technologies
- Next-generation sequencing (NGS)
- Single-cell sequencing
- RNA-seq
- Microarray analysis
News & Updates
Participation in a seminar on December 5, 2018, at the Institute of General Pathology, Policlinico Umberto I.
Presentation of the new Smart&Start Incentive by Invitalia on January 30, 2015.
Participation from May 17 to 19, 2016, at the University of Salerno.
Participation from June 20 to 24, 2016, in Belgrade, Serbia.
Participation from September 10 to 12, 2015, in Naples, Italy.
Workshop from June 6 to 10, 2016, at the University of Naples Federico II.
Participation in a seminar on December 5, 2018, at the Institute of General Pathology, Policlinico Umberto I.
Presentation of the new Smart&Start Incentive by Invitalia on January 30, 2015.
Participation from May 17 to 19, 2016, at the University of Salerno.
Participation from June 20 to 24, 2016, in Belgrade, Serbia.
Participation from September 10 to 12, 2015, in Naples, Italy.
Workshop from June 6 to 10, 2016, at the University of Naples Federico II.