Bioinformatics, Genomics
compleasm. A genome completeness evaluation tool based on miniprot
256longcallR. longcallR is a tool for SNP calling, haplotype phasing, and allele-specific analysis with long-read RNA-seq data.
94NanoSNP. A deep learning-based SNP calling method to identify SNPs based on low-coverage Nanopore sequencing reads.
21BlockPolish. BlockPolish: accurate polishing of long-read assembly via block divide-and-conquer
17SACall-basecaller. Python
16longcallR-nf. Nextflow
10NeuralPolish. NeuralPolish: a novel Nanopore polishing method based on alignment matrix construction and orthogonal Bi-GRU Networks.
9longcallR-nn. longcallR_nn is a variant caller specifically designed for long-read RNA-seq data, utilizing a ResNet50 model.
7PrimFilt. A long-read RNA-seq internal priming detection and filtering tool
5rust-fastqtl. A Rust reimplementation of the core FastQTL cis-QTL mapping logic.
5longcallR_scripts. Jupyter Notebook
2variant_detection_nf. Nextflow
2BPFGM. BlockPolish feature generation module (BPFGM) is used to divide the draft assembly into blocks from reads-to-assembly alignment and generate feature matrices used for predicting consensus sequence.
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