readhit
Browser-based viewer that maps sequencing reads onto one short reference — an amplicon, gene or plasmid. Reads open as Sanger AB1/ABIF, SCF, FASTA, FASTQ or a SAM somebody else already mapped (gzipped files are unpacked in place); the reference as FASTA, GenBank or a read. Both read orientations are tried automatically. The pileup reports per-position depth, where reads disagree with the target, and the consensus — phred-weighted for capillary reads, which keep their chromatogram under the letters. An optional protein lane translates target and consensus side by side. Reads are placed by minimap2 compiled to WebAssembly, or by the built-in aligner. One read or the whole alignment saves as FASTA. Runs entirely in the browser — files are never uploaded.
Topics
Collections
Details
- License:
- Freeware
- Maturity:
- Emerging
- Cost:
- Free of charge
- Tool Type:
- web application
- Operating Systems:
- Linux, Mac, Windows
- Programming Languages:
- TypeScript
- Added:
- 8/21/2026
- Last Updated:
- 8/21/2026
Operations
Data Inputs & Outputs
Chromatogram visualisation
Inputs
Outputs
Pairwise sequence alignment
Documentation
Training material
https://fishka.bio/readhit/showcaseShowcase gallery — an annotated screenshot per task, from a handful of Sanger reads to an NGS pileup opened from a SAM