Between 2013 and 2016, we received a wide range of inquiries from academic and industry researchers. The selected examples below reflect how we engaged with researchers and offered guidance — even as technologies and best practices were rapidly evolving. While the details may now be dated, the clarity, technical depth, and problem-solving mindset remain as relevant as ever.
For more on what sets us apart, explore 10 key advantages of using our services or browse our bioinformatics blog collection.
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Assembling WGS data for marker identification (4/18/2016)
Genome assembly with PacBio data (4/17/2016)
Statistical considerations for metabolomics data analysis (4/4/2016)
RNA-seq analysis pipeline focusing on long ncRNAs (3/11/2016)
Whole-genome sequencing analysis options for human samples (2/6/2016)
Homology-based search vs. pattern-based search (1/5/2016)
"Advanced" Analysis Options for miRNA-Seq Data (12/23/2015)
Identifying Structural Changes in Genome with Short-Read Sequencing Data (12/12/2015)
A Biomarker or Classification Modeling Project (11/7/2015)
Variant Calling Using RNA-seq Data, and Splice Isoform Analysis (11/2/2015)
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