HIT Bioinformatics Centre

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1. HitSV HitSVPublic

   HitSV: Maximizing discovery of structural variants across sequencing technologies

   C 28 1

2. LAMSA LAMSAPublic

   Forked from yangao07/LAMSA

   Long Approximate Matches-based Split Aligner

   C 13 2

3. deSAMBA deSAMBAPublic

   deSAMBA: fast and accurate classification of metagenomics long reads with sparse approximate matches

   C 12 5

4. deBGA deBGAPublic

   Forked from HongzheGuo/deBGA

   de Bruijn Graph-based read aligner

   C 11 5

5. deBWT deBWTPublic

   Forked from DixianZhu/deBWT

   A efficient method to construct BWT index of a given DNA sequence, especially useful for gigantic and high similar genome.

   C 6 1

6. rMETL rMETLPublic

   Forked from tjiangHIT/rMETL

   rMETL - realignment-based Mobile Element insertion detection Tool for Long read

   Python 6