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Tools using SeqAn

Simon Gene Gottlieb edited this page Sep 28, 2022 · 9 revisions

Tools based on:

Seqan3

  • Raptor - A fast and space-efficient pre-filter for querying very large collections of nucleotide sequences
  • iGenVar - A caller for all types of genetic variation: SNPs, indels and larger structural variations (insertions, deletions, inversions, translocations, CNVs, nested SVs). It uses both Illumina short reads and PacBio long reads for this purpose.
  • Chopper - A tool for partitioning a set of sequences into similar batches.
  • Lambda3 - The Local Aligner for Massive Biological DatA
  • Needle - A fast and space-efficient pre-filter for estimating the quantification of very large collections of nucleotide sequences
  • Mars - Motif-based aligned RNA searcher
  • Minions - Comparison between different methods to simplify sequence data
  • RLM - Read level DNA methylation analysis of bisulfite converted sequencing data
  • SeqAn3 Tools - Some helper tools/Demonstration of the library

Seqan2

  • Lambda - The Local Aligner for Massive Biological DatA
  • Lara - LaRA 2: Lagrangian Relaxed structural Alignment
  • Vaquita - Identifies structural variations using split-reads, discordant read-pairs, soft-clipped reads, and read-depth information
  • SLIMM - Species Level Identification of Microbes from Metagenomes
  • Anise & Basil - Methods for the detection and assembly of novel sequence in high-throughput sequencing data
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