Long read based human genomic structural variation detection with cuteSV
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Updated
Dec 13, 2024 - Python
Long read based human genomic structural variation detection with cuteSV
🌈Scaffold genome sequence assemblies using linked or long read sequencing data
Small variant, structural variant, and short tandem repeat phasing tool for PacBio HiFi reads
SpecHLA reconstructs entire diploid sequences of HLA genes and infers LOH events. It supports HLA-A, -B, -C, -DPA1, -DPB1, -DQA1, -DQB1, and -DRB1 genes. Also, it supports both short- and long-read data.
LRSDAY: Long-read Sequencing Data Analysis for Yeasts
rMETL - realignment-based Mobile Element insertion detection Tool for Long read
rMETL - realignment-based Mobile Element insertion detection Tool for Long read
Pipeline to provide high accuracy single molecule consensus sequences from PacBio data using unique molecular identifiers (UMIs).
The `pacmill` python package is a bioinformatics pipeline that is developed to process microbial 16S amplicon sequencing data and produce PDF reports detailing taxonomical assignments along with other statistics.
A workflow for processing CCS reads of AMF to ASVs using DADA2
Hormiphora californensis genome annotation and supplemental materials related to the genome assembly.
A set of tootkit for dealing with COI amplicons using Pacbio sequencing platform
a streamlit application for graphical analyisis of pacbiohifi reads
profiling pacbiokmers and filtering pacbio kmers
pacbiohifi read analyzer using recursion
De novo repeat inference from long reads
SMP: A Salmonella Methylation analysis Pipeline
pacbiohifi report classifier for any sequencing startups
Inter-sample analysis of SQANTI classifications
pacbioHifi genome assembly benchmarks
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