armintoepfer/split2del
Bioinformatics tool to merge split read alignments to reconstruct large deletions.
Toolkit for PrimerID NGS experiments
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Bioinformatics tool to merge split read alignments to reconstruct large deletions.
SequenceAlignmentFixer, a multitude of alignment statistics and fixes for Next Generation Sequencing (NGS) data. Computes consensus sequence with in-frame deletions and insertions.
Creating profiles for SimSeq from BAM alignments and a set of reference genomes.
Visualisation of viral populations