Toolkit for calling structural variants using short or long reads
Tool to annotate outfiles from ExpansionHunter and TRGT with the pathologic implications of the repeat
A Python library to visualize and analyze long-read transcriptomes
A package for analyzing allele-specific expression in polyploid organisms
Nanopore Direct RNA-seq Transcriptome Assembly
No description available
Quality control tool for long read sequencing data
preqclr is a software tool that reports on quality for long read sequencing data without the use of a reference genome.
