Bioinformatics research at Cardiff University
gw. Genome browser and variant annotation
396dysgu. Toolkit for calling structural variants using short or long reads
115superintervals. Fast interval intersection library
45pywfa. Python wrapper for wavefront alignment using WFA2-lib
39SV_Benchmark_CMRG_GIAB. Structural variant benchmark
24svbench. Benchmark structural variant calls against a reference set
18gwplot. Plot genomics data fast
11SV_benchmark_PacBio_HiFi. Structural variant benchmark using PacBio HiFi reads
6superintervalsr. Fast interval intersection queries
4kmerhash. Convert python string to hashed kmers and back again
3zights. htslib for the zig build system
3RemoveCramTags. Quickly remove tag(s) from SAM/BAM/CRAM files
2sortedintersect. Fast intersection of sorted reference intervals
2fnfi. fnfi is a set of tools for aiding split-read alignment and identify structural variants
2ref_genomes. A collection of reference genomes
1dodi. Cython
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