DeepConsensus uses gap-aware sequence transformers to correct errors in Pacific Biosciences (PacBio) Circular Consensus Sequencing (CCS) data.
- Updated
Mar 11, 2025 - Python
DeepConsensus uses gap-aware sequence transformers to correct errors in Pacific Biosciences (PacBio) Circular Consensus Sequencing (CCS) data.
ClairS - a deep-learning method for long-read somatic small variant calling
Graph-based assembly phasing
ClairS-TO - a deep-learning method for tumor-only somatic variant calling
Long-read splice alignment with high accuracy
Single cell Nanopore sequencing data for Genotype and Phenotype
Bioinformatics pipeline for recovery and analysis of metagenome-assembled genomes
A workflow for enhanced protein isoform detection through integration of long-read RNA-seq and mass spectrometry-based proteomics.
Tool to annotate outfiles from ExpansionHunter and TRGT with the pathologic implications of the repeat
Clair3-RNA - a long-read small variant caller for RNA sequencing data
Melon: metagenomic long-read-based taxonomic identification and quantification using marker genes
NANOME pipeline (Nanopore long-read sequencing consensus DNA methylation detection method and pipeline)
An algorithm for centromere assembly using long error-prone reads
Lemur is a tool for rapid and accurate taxonomic profiling on long-read metagenomic datasets
Lightweight bioinformatics pipeline for microbial genome recovery
A short tandem repeat (STR) genotyping and analysis toolkit for long reads
A framework for extracting telomeric reads from single-molecule sequencing experiments, describing their sequence variation and motifs, and for haplotype inference.
🔬 Genotyping tool for genome-edited samples using nanopore-targeted sequencing
A reproducible and scalable workflow for Long Amplicon Consensus Analysis (LACA)
Coronavirus (SARS-Cov-2) sequencing analysis
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