illumina
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An ultra-fast all-in-one FASTQ preprocessor (QC/adapters/trimming/filtering/splitting/merging...)
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Nov 28, 2024 - C++
SPAdes Genome Assembler
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Mar 11, 2025 - C++
Clair3 - Symphonizing pileup and full-alignment for high-performance long-read variant calling
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Feb 28, 2025 - Python
A collection of scripts and notes related to genomics and bioinformatics
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Feb 10, 2025 - R
Amplicon sequencing analysis workflow using DADA2 and QIIME2
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Mar 12, 2025 - Nextflow
Viral genomics analysis pipelines
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Sep 20, 2024 - Python
Aligns short reads using dynamic seed size with strobemers
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Mar 18, 2025 - C++
Highly parallelised multi-taxonomic profiling of shotgun short- and long-read metagenomic data
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Mar 13, 2025 - Nextflow
Assembly and intrahost/low-frequency variant calling for viral samples
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Jan 27, 2025 - Nextflow
Comprehensive TE insertion identification with WGS/WES data from multiple sequencing technics
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Feb 18, 2025 - Python
Command line utility for manipulating Illumina-generated FASTQ files.
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Feb 28, 2025 - Rust
An accurate and ultra-fast hybrid genome assembler
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Apr 10, 2024 - Perl
ClairS - a deep-learning method for long-read somatic small variant calling
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Feb 27, 2025 - Python
Analysis pipelines for genomic sequencing data
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Mar 17, 2025 - Shell
Allelic decomposition and exact genotyping of highly polymorphic and structurally variant genes
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Feb 12, 2025 - C
ClairS-TO - a deep-learning method for tumor-only somatic variant calling
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Mar 10, 2025 - Python
Multi-platform genome assembly pipeline for Illumina, Nanopore and PacBio reads
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Sep 9, 2024 - Nextflow
Parse Illumina sample sheets with Python
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Mar 20, 2024 - Python
Demultiplexing pipeline for sequencing data
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Mar 6, 2025 - Nextflow
R package for the recount2 project. Documentation website:http://leekgroup.github.io/recount/
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Dec 12, 2024 - R
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