inGAP-sv is a structural variation detection and visualization app. The tool can refine short-read alignment by re-aligning short reads around a putative SV. In addition, it can detect large-size structural variations using paired-end sequencing reads. Further, it allows you to visualize SAM-formatted alignments and SVs.
Sequencher works with all automated DNA sequencers and is widely known for its lightning-fast contig assembly...
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