Alternatives and similar repositories for daylily:

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

• GooglingTheCancerGenome / sv-channels
  Deep learning-based structural variant filtering method
  ☆38Updated last year
• brentp / fraguracy
  overlapping bases in read-pairs from a fragment indicate accuracy and reveal error-prone sites
  ☆31Updated 3 weeks ago
• fulcrumgenomics / fqtk
  Fast FASTQ sample demultiplexing in Rust.
  ☆58Updated last month
• myriad-opensource / samwell
  Samwell: a python package for using genomic files... well
  ☆19Updated 2 years ago
• awslabs / linter-rules-for-nextflow
  Linter rules for Nextflow DSL scripts
  ☆29Updated last month
• dwpeng / filterx
  process any file in tabular format. Fasta/fastq/GTF/GFF/VCF/SAM/BED
  ☆21Updated 2 weeks ago
• InscriptaLabs / BioCantor
  ☆21Updated last year
• brentp / vcfexpress
  expressions on VCFs
  ☆66Updated this week
• telatin / covtobed
  ⛰ covtobed | Convert the coverage track from a BAM file into a BED file
  ☆43Updated 2 years ago
• vembrane / vembrane
  vembrane filters VCF records using python expressions
  ☆58Updated 4 months ago
• rhpvorderman / sequali
  Fast sequencing data quality metrics
  ☆17Updated last month
• jfarek / alignstats
  Comprehensive alignment, whole-genome coverage, and capture coverage statistics.
  ☆19Updated last month
• brentp / tiwih
  simple bioinformatics command-line (t)ools (i) (w)ished (i) (h)ad.
  ☆44Updated last year
• nextflow-io / nf-validation
  Params validation plugin for Nextflow pipelines
  ☆48Updated 5 months ago
• KevinKuchinski / ProbeTools
  Hybridization probe design for targeted genomic sequencing of diverse and hypervariable viral taxa
  ☆23Updated last year
• cpockrandt / PhyloCSFpp
  PhyloCSF++ computes PhyloCSF tracks for whole-genome multiple sequence alignments, scores single MSA, annotates CDS features in GFF/GTF f…
  ☆30Updated 3 years ago
• IARCbioinfo / alignment-nf
  Whole Exome/Whole Genome Sequencing alignment pipeline
  ☆28Updated 4 months ago
• Psy-Fer / blue-crab
  crab go snap snap
  ☆35Updated this week
• alignoth / alignoth
  Creating alignment plots from bam files
  ☆56Updated this week
• jts / bri
  Bam Read Index - Extract alignments from a bam file by readname
  ☆24Updated 9 months ago
• seqeralabs / nf-training-advanced
  Customer workshop materials
  ☆17Updated last year
• brianli314 / palindrome-finder
  A bioinformatics tool written in Rust to find palindromic sequences in DNA
  ☆34Updated this week
• Parsoa / SVDSS
  Improved structural variant discovery in accurate long reads using sample-specific strings (SFS)
  ☆42Updated 3 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…
  ☆28Updated 2 months ago
• fulcrumgenomics / prymer
  Python Primer Design Library
  ☆11Updated this week
• Illumina / witty.er
  What is true, thank you, ernestly. A large variant benchmarking tool analogous to hap.py for small variants.
  ☆30Updated last year
• natir / biotest
  Generate random test data for bioinformatics
  ☆25Updated 7 months ago
• mribeirodantas / NextflowSnippets
  This repository hosts a large collection of Nextflow snippets
  ☆57Updated this week
• BonsonW / slow5curl
  A library and tool for accessing remote BLOW5 files.
  ☆24Updated 3 months ago
• Sentieon / sentieon-models
  Model files for Sentieon variant callers
  ☆14Updated 5 months ago