Angstrom Innovation provides rapid, affordable nanopore DNA sequencing with next-day data delivery for biotech and academic labs. The company offers same-day dropbox pickup across the SF Bay Area and mail-in service nationwide, with any plasmid up to 30 kbp sequenced for $7. Their service includes FASTQ data, automated annotations, and plasmid assembly, supported by PhD-level scientists for data interpretation.
- Biotechnology
- Healthcare Technology
Funding
Founders
Product
Problem
Biotech teams and academic labs often face slow turnaround times and high costs when outsourcing DNA sequencing, which delays research progress and strains limited budgets. Traditional sequencing services can take days or weeks to return results, creating bottlenecks in iterative experimental workflows.
Solution
Angstrom Innovation provides high-quality nanopore DNA sequencing with industry-leading prices and rapid turnaround. Customers can order by 3pm Pacific for Bay Area dropbox pickup or have samples arrive by 4pm Pacific via mail-in service, with data returned overnight by 8am the next business day. The service sequences any plasmid up to 30 kbp for a flat $7, including FASTQ data, automated annotations, and plasmid assembly. PhD scientists from top institutions provide expert support to help customers interpret NGS data, build references, and investigate mutations.
Target Audience
Primary customers are biotech teams and academic labs that need fast, affordable DNA sequencing with expert support for data analysis and interpretation.
Features
- Next-day data delivery with orders placed by 3pm Pacific (Bay Area) or samples arriving by 4pm Pacific, with results available by 8am the next morning, Monday–Friday
- Flat-rate pricing of $7 per plasmid up to 30 kbp, including FASTQ data, automated annotations, and plasmid assembly
- Same-day dropbox pickup across the SF Bay Area and mail-in service available from anywhere in the US
- Nanopore sequencing technology for long-read, high-accuracy data generation
- Expert support from PhD scientists for NGS data interpretation, reference building, and mutation analysis