AA Bio Consulting
NGS Data Analysis for Research Labs
You generate the sequencing data. I turn it into publication-ready results.
Meet the Expert
Founder, AA Bio Consulting
I help research labs analyze their next-generation sequencing data — RNA-seq, whole genome, metagenomics, amplicon — so they can publish faster and move on to the next experiment.
I hold dual master's degrees from Johns Hopkins University in Bioinformatics and Biotechnology Enterprise & Entrepreneurship, and a B.S. in Cell and Molecular Biology from Binghamton University. My background includes designing and managing a bioinformatics database integrating phenotypic and genomic data for tree disease research at SilvaBio, as well as previous roles at Myriad Genetics and Novogene.
If your lab has sequencing data that needs to be processed, analyzed, and turned into figures and methods you can drop straight into a manuscript, that's exactly what I do.
Connect with me on LinkedIn.
Our Services
What I Do
You send me your raw sequencing data. I send you back clean, publication-ready results. The typical project takes 2-4 weeks from FASTQ files to final deliverables.
RNA-Seq & Differential Expression Analysis
QC
Alignment
Normalization
Differential expression
Pathway enrichment
Publication-ready figures and methods
Whole Genome & Variant Analysis
Alignment
Variant calling
Annotation
Filtering for population genomics, crop genetics, conservation biology, or disease-resistance studies.
Metagenomics & Amplicon Analysis
Community profiling
Diversity analysis
Taxonomic characterization for environmental, soil, microbiome, or phycology research.
Custom Pipeline Development
If your lab generates sequencing data regularly, I can build you a reproducible, documented pipeline you run yourself going forward.
Every project includes a results report with figures, a methods section ready for your manuscript, the underlying data files, and a walkthrough call to discuss the findings.
All services can be delivered as fixed-price projects or flexible retainers, depending on your preference.
Your sequencing data shouldn't sit on a hard drive waiting for someone to analyze it.
If your lab has NGS data that needs processing — whether it's a one-time analysis or ongoing support — I can help you move from raw reads to publishable results in weeks, not months.
Contact Us
I work with academic research labs, biotech startups, and agritech teams who need bioinformatics analysis done right.
Reach out to discuss your project or schedule a free 15-minute scope call.