We offer tailored bioinformatics services (mainly NGS data analysis) to academic and private organizations. We have a strong academic background with a focus on cutting edge, open source software.
We build up your in-house bioinformatics capacity in 2 ways: First, we provide you with the code underlying the analysis you requested. Second, we can help you to set up (cloud) computing solutions that will allow you to run and extend your analyses on your own.
We replicate recommended analysis pipelines (best practice) or develop novel ones. We put a premium on the biological insights you can get from your data.
Analysis of your RNA-seq data using a "best practice" pipeline (e.g. tophat/cufflinks, DEseq2, ...).
Our analysis includes quantitation (FPKM), differential expression, scatterplots, heatmaps (hierarchical clustering) or PCA (principal component analysis).
We will customize our analysis to your specific needs: we can perform quality control of your raw data, double check your experimental design and provide a written report of our analysis methods (publication-ready).
Price: $150 USD per sample for the first 6 samples, $100 USD per sample for additional samples.
"Best practice" or customized bioinformatics analyses for your genomic data:
SNP and Indel genotyping
Structural variant detection
Detection of somatic mutations
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