DNA Sequence Analysis Tool - Discovery Questions

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Your Current Workflow

01What does your typical sequence analysis workflow look like today?

Walk me through what you do from the moment you have a sequence to when you get the answers you need.

02What tools do you currently use?

NCBI Web Interface (BLAST, etc.) Geneious SnapGene Benchling Command-line BLAST Custom scripts (Python, R, etc.) Other (please specify below)

03What's the most frustrating or time-consuming part of your current process?

04How often do you perform sequence analysis?

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Your Sequences & Analysis Needs

05What types of sequences do you typically work with?

Gene fragments, full genes, plasmids, primers, genomic regions, etc. What's the typical length?

06What questions are you usually trying to answer?

Identify unknown sequences ("What gene is this?") Verify cloned sequences ("Is this the right clone?") Find similar sequences in other species Check for mutations or variants Verify PCR products Primer design or validation Other (please specify below)

07Which NCBI databases do you query most often?

08Do you need protein translation or just DNA-level analysis?

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Output & Records

09How would you like to receive results?

Email with results Google Sheets / Excel spreadsheet Downloadable PDF report Web interface / dashboard Raw data files (FASTA, JSON, etc.)

10Do you need to keep records for publications or lab notebooks?

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Other Considerations

11Any restrictions on using cloud-based tools with your sequence data?

Unpublished sequences, IP concerns, institutional policies, etc.

12If you could wave a magic wand, what would the perfect tool do for you?

Your Name

Your Email

Responses will be sent to info@joelutai.com

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Thank You!

Your responses have been submitted. We'll review them and get back to you soon with a tailored solution.