Alternatives and similar repositories for VCF2Dis:

Users that are interested in VCF2Dis are comparing it to the libraries listed below

• BGI-shenzhen / RectChr
  Multi-level visualization of genomic statistical variables on rectangular chromosomes
  ☆86Updated 2 months ago
• hardingnj / xpclr
  Code to compute the XP-CLR statistic to infer natural selection
  ☆93Updated 2 years ago
• chenlianfu / geta
  ☆73Updated 7 months ago
• steuernb / NLR-Annotator
  NLR-Annotator upload
  ☆63Updated last year
• 4ureliek / Parsing-RepeatMasker-Outputs
  Few scripts facilitating the extraction of info from Repeat Masker .out files
  ☆78Updated 3 years ago
• xuzhougeng / Genomic_tools
  Genomic related tools
  ☆71Updated 3 years ago
• fanagislab / GCE
  GCE (genomic charactor estimator) is a bayes model based method to estimate the genome size, genomic repeat content and the heterozygsis…
  ☆48Updated 4 years ago
• hewm2008 / VCF2PCACluster
  A new simple and efficient software to PCA and Cluster For popolation VCF File
  ☆68Updated last week
• voichek / kmersGWAS
  A library for running k-mers based GWAS
  ☆106Updated 3 months ago
• qiao-xin / DupGen_finder
  A pipeline used to identify different modes of duplicated gene pairs
  ☆95Updated 4 years ago
• xiaochuanle / MECAT2
  ☆70Updated 4 years ago
• tbenavi1 / genomescope2.0
  Reference-free profiling of polyploid genomes
  ☆112Updated 7 months ago
• speciationgenomics / scripts
  Scripts for analysis used during the course
  ☆87Updated 9 months ago
• YangJianshun / LINKVIEW2
  DNA序列比对结果 可视化展示工具
  ☆45Updated 2 years ago
• wk8910 / bio_tools
  Useful bioinformatic scripts
  ☆54Updated 2 months ago
• tpoorten / dotPlotly
  Generate an interactive dot plot from mummer or minimap alignments
  ☆195Updated last year
• quxiaojian / PGA
  Plastid Genome Annotator
  ☆49Updated 4 years ago
• thlee / SNPhylo
  A pipeline to generate a phylogenetic tree from huge SNP data
  ☆86Updated last year
• nt246 / lcwgs-guide-tutorial
  ☆82Updated 3 years ago
• BGI-shenzhen / Reseqtools
  A Toolkit for analyzing next-generation DNA Re-Sequencing data
  ☆82Updated 3 years ago
• szpiech / selscan
  Haplotype based scans for selection
  ☆120Updated this week
• HongboDoll / TomatoSuperPanGenome
  Here, we sequence and de novo assemble chromosome-scale genomes of nine wild species and two cultivated accessions of tomato and construc…
  ☆50Updated 8 months ago
• YuSugihara / MutMap
  MutMap pipeline to identify causative mutations responsible for a phenotype
  ☆52Updated 2 weeks ago
• YaoZhou89 / TGG
  tomato graph pangenome
  ☆79Updated 2 years ago
• popgenmethods / smcpp
  SMC++ infers population history from whole-genome sequence data.
  ☆159Updated last year
• hyphaltip / genome-scripts
  Genome Scripts used in fungal comparative genomics
  ☆65Updated 4 years ago
• sujaikumar / assemblage
  Tools for working with second gen assemblies, fasta sequences, etc
  ☆92Updated 8 years ago
• mahulchak / svmu
  A program to call variants from genome alignment
  ☆78Updated 10 months ago
• yjx1217 / RMRB
  This is an archive version of old RepBase library (v20170127) for RepeatMasker.
  ☆29Updated 3 years ago
• irusri / Extract-intron-from-gff3
  This script will extract the intron feature gff3 and sequence from gene_exon gff3 and fasta file.
  ☆33Updated 6 years ago