There are 1 repository under pacbio-sequencing topic.
A battery of methylation tools for PacBio HiFi reads
NanoRepeat: fast and accurate analysis of Short Tandem Repeats (STRs) from Oxford Nanopore sequencing data
Detect and phase minor SNVs from long-read sequencing data
A systematic survey of algorithmic foundations and methodologies across 107 alignment methods (1988-2021), for both short and long reads. We provide a rigorous experimental evaluation of 11 read aligners to demonstrate the effect of these underlying algorithms on speed and efficiency of read alignment. Described by Alser et al. at https://arxiv.org/abs/2003.00110.
genome assembly to pangraphs from illumina to long reads.
Identify and characterize repeat expansions in long read data
pacbio or oxford nanopore long reads repeat coverage estimation.
Patch for LRSDAY v1.6 for Debian-based and SUSE-based OS.
code getter for illumina, pacbio, oxford long reads alignments.
awk code for pacbiohifi alignments from verkko and other genome assembly methods
bcftools for dealing with bcf files.
a conda yaml for the genomehifi-contiguity analysis.
lastz alignment sorting and plotting the alignment length
pattern detection in R using the stringR package for the pacbio and the oxford nanopore reads
long_read_polyATGC_trimmer using regular expression.
a pacbiohifi read check for the quick view of the read types.
pacbiohifi sequencing genomes analysis using the verkko, hifiasm and the genomeasm4pg.