genome analysis server

BAM file statistics.

Heuristic barcode generator.

Visualize the per-position base distribution across multiple DNA sequences.

Browse haplotype-resolved data, such as Strand-seq.

Rapid InDel Discovery in Sanger Chromatograms.

Visually align sequences using exact matches.

Padlock probe design for in-situ sequencing.

Assemble trace files with an optional reference sequence.

Pick primers from a DNA sequence.

Tools to handle RDML files.

Sequence alignment browser.

Sanger trace alignment.

Affine gap local and banded global alignment for two DNA sequences.

In-silico PCR amplification on complete genomes.

Trace analysis viewer.

Visualize aligned reads.

Edit DNA sequences, reverse-complement and do restriction digests.