Haplotype-aware analysis toolkit for long-read sequencing data
vechat. Correcting errors in noisy long reads using variation graphs
52Strainline. Full-length de novo viral haplotype reconstruction from noisy long reads
21DiseaseCapsule. Predicting the prevalence of complex genetic diseases from individual genotype profiles using capsule networks
15HERO. Hybrid error correction approach for long reads using overlap graph
11HyLight. HyLight is a strain aware de novo assembly method based on the overlap-layout-consensus (OLC) paradigm that leverages the strengths of NGS and 3rd generation sequencing to rapidly and accurately assemble highly complex metagenomic sequencing data.
8metagenome-asm. Enhancing long read based strain-aware metagenome assembly
2CrossHyLight. CrossHyLight is a strain aware de novo assembly method based on the overlap-layout-consensus (OLC) paradigm that leverages the strengths of NGS and 3rd generation sequencing to rapidly and accurately assemble highly complex metagenomic sequencing data.
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