Pay-per-use and flexible bioinformatics: Standard and premium packages to provide the exact desired solution.
Transcriptome

RNA-seq experiments are an efficient way to measure transcriptome data to get information such as how different alleles of a gene are expressed, detect post-transcriptional mutations or identify gene fusions.
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RNAseq Brochure
Assotiation Studies

Genome-wide Assotiation Studies (GWAS) is an examination of many common genetic variants in different individuals to see if any variant is associated with a trait, typically focus on associations between single-nucleotide polymorphisms (SNPs) and traits like major diseases or concrete phenotypes.
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GWAS BrochureChIP-Seq

ChIP–seq is a technique for genome-wide profiling of DNA-binding proteins, histone modifications or nucleosomes. ChIP–seq offers higher resolution, less noise and greater coverage than its array-based predecessor ChIP–chip.
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ChIP-Seq Brochuresmall RNAs

Small non-coding RNAs are typically only ~18–40 nucleotides in length, with a relevant functional impact in developmental timing, cell fate, tumor progression and neurogenesis. With this technology, researcher can detect miRNA profile, discover novel miRNA and create a full characterization of novel classes with an unknown function nowadays.
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miRNA BrochureDe novo Assembly

In such cases where reference genome is not available, the first step implies generating the assembly, called de novo sequencing.
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Denovo Assembly BrochureMetagenomics

Metagenomics is the study of the genetic material recovered directly from environmental samples, to produce a profile of diversity. Discover those microbial biodiversity missed by cultivation-based methods.
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Microarray Analysis

We offer a wide variety of microarray data analysis services, both commercial and customized, for the main applications such as gene expression, epigenetics, SNP discovery, or biomarker assotiation. Contact us for your specific requirements.
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