SeqBench: DNA sequence analysis in your browser

Paste a DNA sequence or FASTA record and instantly see its composition, reverse complement, translations in all six reading frames, open reading frames, and motif matches.

Open SeqBenchAll tools

Free, no sign-up, and installable on your phone. Runs in your browser at seqbench.gataca.com.

SeqBench showing results for the built-in example
SeqBench with its built-in example loaded.

What you can do with SeqBench

  • Check GC content and length before ordering a synthetic gene
  • Get a reverse complement or RNA transcript without retyping
  • Find open reading frames in a cloned insert or contig
  • Locate restriction sites, promoters, or other motifs, including IUPAC patterns

How to use it

  1. Paste a DNA sequence or FASTA record. Spaces, numbers, and headers are cleaned up automatically.
  2. Read the summary: length, GC and AT content, estimated Tm, and molecular weight.
  3. Switch tabs for the reverse complement, RNA, six-frame translation, or ORF list.
  4. Type a motif to highlight every match on both strands.

Features

  • GC and AT content with a base composition bar
  • Reverse complement and RNA transcription with one-click copy
  • Six-frame translation using the standard genetic code
  • ORF finder with adjustable minimum length
  • IUPAC motif search on both strands
  • Estimated melting temperature and molecular weight
  • Save results as reports, spreadsheets, or sequence files
  • Install it on your phone or computer; works offline

Frequently asked questions

Is SeqBench free?

Yes. SeqBench is free to use with no account or sign-up.

How is the melting temperature estimated?

Short sequences (under 14 bases) use the Wallace rule; longer ones use a GC-based formula. For primer Tm with salt correction, use PrimerBench.

How long can my sequence be?

Analysis works on sequences of any practical length; the colored sequence view shows the first 20,000 bases to keep the page fast.

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Need SeqBench to do more?

We build custom versions and full pipelines for research teams.

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