DeepConsensus uses gap-aware sequence transformers to correct errors in Pacific Biosciences (PacBio) Circular Consensus Sequencing (CCS) data.
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Updated
Oct 9, 2024 - Python
DeepConsensus uses gap-aware sequence transformers to correct errors in Pacific Biosciences (PacBio) Circular Consensus Sequencing (CCS) data.
Assembly and binning of metagenomes
Assembly and intrahost/low-frequency variant calling for viral samples
ClairS - a deep-learning method for long-read somatic small variant calling
Graph-based assembly phasing
Long-read splice alignment with high accuracy
ClairS-TO - a deep-learning method for tumor-only somatic variant calling
Fast and space-efficient taxonomic classification of long reads
Single cell Nanopore sequencing data for Genotype and Phenotype
A workflow for enhanced protein isoform detection through integration of long-read RNA-seq and mass spectrometry-based proteomics.
A pipeline for high-quality bacterial genome construction using ONT sequencing
Bioinformatics pipeline for recovery and analysis of metagenome-assembled genomes
Linear-time de novo Long Read Assembler
scisorseqr is an R-package for processing of single-cell long read data and analyzing differential isoform expression across any two conditions
Efficient and accurate pathogenicity prediction for coding and regulatory structural variants in long-read genome sequencing
Melon: metagenomic long-read-based taxonomic identification and quantification using marker genes
Tool to annotate outfiles from ExpansionHunter and TRGT with the pathologic implications of the repeat
NANOME pipeline (Nanopore long-read sequencing data consensus DNA methylation detection)
An algorithm for centromere assembly using long error-prone reads
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