Alternatives and similar repositories for kyber

Users that are interested in kyber are comparing it to the libraries listed below

• wdecoster / phasius
  ☆16Updated 5 months ago
• 1kg-ont-vienna / sv-analysis
  SV analysis of the long-read sequencing data of the 1019 samples of the 1KG-ONT panel
  ☆38Updated 7 months ago
• Parsoa / SVDSS
  Improved structural variant discovery in accurate long reads using sample-specific strings (SFS)
  ☆46Updated 3 months ago
• alejandrogzi / gtfsort
  a lexicographically-based GTF/GFF sorter
  ☆35Updated 7 months ago
• JustinChu / ntsm
  This tools counts the number of specific k-mers within sequence data. The counts can then be compare to other counts to determine to comp…
  ☆30Updated last year
• nanoporegenomics / napu_wf
  WDL workflows for variant calling and assembly using ONT
  ☆38Updated 2 months ago
• jts / smrest
  Tumour-only somatic mutation calling using long reads
  ☆28Updated last year
• noamteyssier / gia
  gia: Genomic Interval Arithmetic
  ☆63Updated last year
• EliseCoopman / methylmap
  Methylmap is a tool for visualization of modified nucleotide frequencies for large cohort sizes.
  ☆21Updated 9 months ago
• pierrepeterlongo / back_to_sequences
  ☆45Updated 3 weeks ago
• HudsonAlpha / fmlrc2
  ☆49Updated 2 years ago
• alignoth / alignoth
  Creating alignment plots from bam files
  ☆69Updated 3 weeks ago
• Psy-Fer / blue-crab
  lossless nanopore pod5 <=> s/blow5 file conversion
  ☆44Updated 3 months ago
• PacificBiosciences / sawfish
  Joint structural variant and copy number variant caller for HiFi sequencing data
  ☆65Updated last month
• micahvista / VACmap
  VACmap: a long-read aligner specifically designed for complex structural variation discovery
  ☆37Updated this week
• pangenome / impg
  implicit pangenome graph
  ☆84Updated last week
• brentp / vcfexpress
  expressions on VCFs
  ☆87Updated 7 months ago
• ACEnglish / kanpig
  Kmer Analysis of Pileups for Genotyping
  ☆34Updated last week
• lh3 / longdust
  Identify long STRs, VNTRs, satellite DNA and other low-complexity regions in a genome
  ☆82Updated 2 weeks ago
• lh3 / panmask
  Easy genomic regions for short-read variant calling
  ☆45Updated 3 months ago
• marbl / T2T-Browser
  Genome browser hub for the T2T genomes and resources
  ☆25Updated 2 months ago
• SouthGreenPlatform / panache
  Panache is a web-based interface designed for the visualization of linearized pangenomes. It can be used to show presence/absence informa…
  ☆45Updated 2 years ago
• PacificBiosciences / svpack
  Structural variant (SV) analysis tools
  ☆39Updated last year
• PacificBiosciences / MethBat
  A battery of methylation tools for PacBio HiFi reads
  ☆44Updated last week
• ComparativeGenomicsToolkit / taffy
  This is a library C/Python/CLI for working with TAF (.taf,.taf.gz) and MAF (.maf) alignment files
  ☆29Updated 3 months ago
• dashnowlab / STRchive
  Short Tandem Repeat disease loci resource
  ☆24Updated this week
• brianli314 / palindrome-finder
  A bioinformatics tool written in Rust to find palindromic sequences in DNA
  ☆38Updated 3 months ago
• natir / fpa
  Filter of Pairwise Alignement
  ☆44Updated 3 years ago
• warp9seq / minimod
  A bioinformatics tool for viewing and calculating base modification frequencies from BAM files
  ☆40Updated this week
• lh3 / calN50
  Compute N50/NG50 and auN/auNG
  ☆33Updated 2 years ago