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
  ☆39Updated last year
• myriad-opensource / samwell
  Samwell: a python package for using genomic files... well
  ☆20Updated 2 years ago
• vpc-ccg / svict
  Structural Variation and fusion detection using targeted sequencing data from circulating cell free DNA
  ☆28Updated last year
• rhpvorderman / sequali
  Fast sequencing data quality metrics
  ☆26Updated last week
• CoreArray / PySeqArray
  PySeqArray: data manipulation of whole-genome sequencing variants with SeqArray files in Python (pre-release version)
  ☆14Updated 7 years ago
• telatin / covtobed
  ⛰ covtobed | Convert the coverage track from a BAM file into a BED file
  ☆44Updated 3 years ago
• varfish-org / mehari
  VEP-like tool for sequence ontology and HGVS annotation of VCF files
  ☆20Updated this week
• Sentieon / sentieon-models
  Model files for Sentieon variant callers
  ☆16Updated last month
• aprilweilab / picovcf
  Single-header C++ library for fast/low-memory VCF (Variant Call Format) parsing.
  ☆17Updated last week
• AstraZeneca-NGS / simple_sv_annotation
  Simplify snpEff annotations for interesting cases
  ☆22Updated 6 years ago
• daihang16 / nubeamdedup
  Removing PCR duplicates for sequencing reads.
  ☆14Updated 4 years ago
• brentp / fraguracy
  overlapping bases in read-pairs from a fragment indicate accuracy and reveal error-prone sites
  ☆33Updated this week
• jfarek / xatlas
  ☆30Updated 2 years ago
• ljdursi / mergevcf
  Python package and routines for merging VCF files
  ☆29Updated 4 years ago
• aquaskyline / 16GT
  Simultaneous detection of SNPs and Indels using a 16-genotype probabilistic model
  ☆27Updated last year
• grailbio / doppelmark
  NGS duplicate marking
  ☆19Updated 4 years ago
• VCCRI / SVPV
  Structural Variant Prediction Viewer
  ☆34Updated 7 years ago
• kehrlab / PopDel
  Population-wide Deletion Calling
  ☆35Updated last month
• tkzeng / GeneBayes
  ☆25Updated last year
• DecodeGenetics / popSTR
  PopSTR - A Population based microsatellite genotyper
  ☆33Updated last year
• sigven / cacao
  Callable Cancer Loci - assessment of sequencing coverage for actionable and pathogenic loci in cancer
  ☆21Updated 4 years ago
• PacificBiosciences / svpack
  Structural variant (SV) analysis tools
  ☆36Updated 11 months ago
• InscriptaLabs / BioCantor
  ☆22Updated last year
• biosails / pheniqs
  Fast and accurate sequence demultiplexing
  ☆28Updated 3 months ago
• ulelab / ultraplex
  Ultra-fast 5' and 3' demultiplexer
  ☆27Updated last year
• seqeralabs / nf-training-advanced
  Customer workshop materials
  ☆18Updated 2 years ago
• vembrane / vembrane
  vembrane filters VCF records using python expressions
  ☆58Updated this week
• Mesh89 / TranSurVeyor
  A transposition caller.
  ☆10Updated last year
• senzhaocode / FuSViz
  A web-browser app to visualise, interpret and prioritise genomic/transcriptomic structural variations (SVs) of multiple samples.
  ☆10Updated last month
• usnistgov / SVClassify
  Hemang Parikh
  ☆11Updated 9 years ago