Aggregate results from bioinformatics analyses across many samples into ...
Structural variation caller using third generation sequencing
genes and genomes at your fingertips
Toolset for SV simulation, comparison and filtering
NGMLR is a long-read mapper designed to align PacBio or Oxford Nanopore ...
Run_dbcan V4, using genomes/metagenomes/proteomes of any assembled organ...
:rocket: seqfu - Sequece Fastx Utilities
Reproducible bioinformatics pipelines in python. Import any Unix tool/co...
Chanjo provides a better way to analyze coverage data in clinical sequen...
⛰ covtobed | Convert the coverage track from a BAM file into a BED file