GENOMIC INVESTIGATION
NIMGenetics, through its R+D Service, offers Researchers and/or Research groups the development of projects based on the latest technologies.
We offer a wide range of genomic tools, for the analysis of models of different species
Massive Sequencing
Next Generation Sequencing (NGS)
The compromise of NIMGenetics with the clinical translation of the advances on genomic research is endless. NIMGenetics is now offering Services that include the use Next Generation Sequencing based on mixed systems of selection/sequencing (Agilent SureSelect®/Solexa/Illumina). This type of sequencing allows to obtain direct data of the sequence of the genome for their use on functional studies that establish the relationship between the changes of the sequence (variations) and the different phenotypes.
Available choices of NGS approaches:
DNA- Sequencing of human whole exome
DNA- Re-sequencing de human whole genome and exome
DNA- Selective or targeted Sequencing
DNA- Re-sequencing of bacterial whole genome
DNA- Re-sequencing of vegetal and animal whole genome de
RNA-Transcriptome
Epigenomics- Sequencing of whole -bysulphited- genome
Epigenomics- MeDIP and ChIP sequencing
For other options, please contact our specialists
Microarray Research
NIMGenetics, at its R+D Department, will facilate to the researchers the development of projects based on the latest technologies of genomic nature including: experimental design, performance of the experiments and bioinformatic assistance during the analysis.
We offer a wide panel of genomic tools for the analysis of several species.
CGH array
Expression arrays
Methylation arrays
Chip-on-Chip arrays
microRNA arrays
Genotyping (SNPs) arrays
Customizes arrays
Bioinformatic analysis
To obtain more information, please contact NIMGenetics.
