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
• 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…
  ☆29Updated 3 months ago
• natir / biotest
  Generate random test data for bioinformatics
  ☆25Updated 8 months ago
• InscriptaLabs / BioCantor
  ☆21Updated last year
• brentp / fraguracy
  overlapping bases in read-pairs from a fragment indicate accuracy and reveal error-prone sites
  ☆33Updated last week
• rhpvorderman / sequali
  Fast sequencing data quality metrics
  ☆24Updated 3 weeks ago
• IARCbioinfo / alignment-nf
  Whole Exome/Whole Genome Sequencing alignment pipeline
  ☆28Updated 5 months ago
• Psy-Fer / blue-crab
  crab go snap snap
  ☆37Updated last month
• huangnengCSU / longcallR
  LongcallR is a small variant caller for single molecule long-read RNA-seq data
  ☆44Updated 4 months ago
• seqeralabs / nf-training-advanced
  Customer workshop materials
  ☆17Updated last year
• myriad-opensource / samwell
  Samwell: a python package for using genomic files... well
  ☆20Updated 2 years ago
• noamteyssier / bedrs
  bedtools-like functionality for interval sets in rust
  ☆49Updated 6 months ago
• 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
• nf-core / variantbenchmarking
  Pipeline to evaluate and validate the accuracy of variant calling methods in genomic research
  ☆23Updated this week
• fulcrumgenomics / fgpyo
  Quality of life improvements for Bioinformatics in Python.
  ☆27Updated last week
• sbg / smart-variant-filtering
  ☆30Updated 4 years ago
• ulelab / ultraplex
  Ultra-fast 5' and 3' demultiplexer
  ☆26Updated 10 months ago
• fulcrumgenomics / fqtk
  Fast FASTQ sample demultiplexing in Rust.
  ☆61Updated this week
• brentp / spacepile
  convert reads from repeated measures of same piece of DNA into spaced matricies for deep learners.
  ☆14Updated last year
• alejandrogzi / gtfsort
  a lexicographically-based GTF/GFF sorter
  ☆32Updated 6 months ago
• brianli314 / palindrome-finder
  A bioinformatics tool written in Rust to find palindromic sequences in DNA
  ☆34Updated last month
• telatin / covtobed
  ⛰ covtobed | Convert the coverage track from a BAM file into a BED file
  ☆43Updated 2 years ago
• jts / smrest
  Tumour-only somatic mutation calling using long reads
  ☆26Updated 4 months ago
• Mesh89 / TranSurVeyor
  A transposition caller.
  ☆10Updated last year
• fmalmeida / MpGAP
  Multi-platform genome assembly pipeline for Illumina, Nanopore and PacBio reads
  ☆58Updated 5 months ago
• nickloman / poredb
  ☆19Updated 7 years ago
• Arcadia-Science / seqqc
  A Nextflow pipeline to identify quality control issues with new sequencing data.
  ☆28Updated 2 years ago
• fulcrumgenomics / prymer
  Python Primer Design Library
  ☆12Updated 2 weeks ago
• HudsonAlpha / CSL_public_benchmark
  Location of public benchmarking; primarily final results
  ☆18Updated 2 weeks ago
• Sentieon / sentieon-models
  Model files for Sentieon variant callers
  ☆14Updated last week