Our Services

Note: This page was prepared for academic customers. Clients from the biotech / pharmaceutical / therapeutic / molecular diagnosis industries, please visit this web site instead.

We provide bioinformatics services to biomedical researchers in academic institutions, biotech and pharmaceutical industries, clinical facilities and government agencies. In addition to providing advice and assistance in the design and the implementation of bioinformatics-heavy research projects, our bioinformatics team directly carries out bioinformatics projects and bioinformatics-heavy components of research projects for our clients. We serve researchers and in diverse domains involving a wide range of organisms - from medical research using human samples or involving human patients, to animal and plant studies using model or non-model organisms, all the way to research projects focusing on microbial and viral species.

We undertake a wide variety of types of bioinformatics work, including but not limited to: processing, analyzing and interpreting high-throughput biological and medical data - with emphasis on next-generation sequencing (NGS) data, genomics, transcriptomics, proteomics, metabolomics and other omics data, statistical data analysis, data integration for diverse biomedical and other data types - e.g., for purposes of identifying causal relationships or other hidden information between measured variables, statistical modeling, machine learning method development and applications, metagenomics, ecology, phylogenetics, population genetics and other analyses related to evolutionary biology, data mining, customized and advanced analysis method development, specific data structure and algorithm development, informatics, database development and maintenance, software solutions, and IT and infrastructure solutions.

Our team is experienced in handling NGS data from all common platforms - including Illumina, Ion Torrent, 454, SOLiD, PacBio and Oxford Nanopore, and for all common NGS applications - including whole-genome sequencing (mapping-based or assembly-based applications), exome and other targeted sequencing, RNA-seq (mapping-based or de novo assembly-based analysis), ChIP-seq (for transcription factors, RNA PolII and histone modifications), and various sequencing-based DNA methylation applications. We are also experienced in less frequently used NGS applications such as DNase-seq, CLIP-seq, 4C-seq, Hi-C, ChIA-PET, and immunosequencing. Furthermore, we are also capable of assisting in developing novel NGS applications.

We are experienced in handling microarray data from all major array platforms (Affymetrix, Agilent, Illumina and NimbleGen), for various applications including gene expression profiling, DNA methylation analysis, genotyping, and others.

See some of the advantages of using our services at this page.

Please click here to see the qualifications and experiences of our bioinformatics experts.

Click here to see how our bioinformatics experts have interacted with researchers and other clients recently.

Click here to view the list of our current clients and partner institutions.

And click here to see our current clients have evaluated our work.

Find out more about our working cycle, pricing information, read our FAQs, send us an inquiry, chat with us online (during our business hours 9-5 Mon-Fri U.S. Central Time), or reach us in other ways!