TruvariStructural variant toolkit for VCFs
Stars: ✭ 85 (-7.61%)
SvtyperBayesian genotyper for structural variants
Stars: ✭ 79 (-14.13%)
GenozipCompressor for genomic files (FASTQ, SAM/BAM, VCF, FASTA, GVF, 23andMe...), up to 5x better than gzip and faster too
Stars: ✭ 53 (-42.39%)
16gtSimultaneous detection of SNPs and Indels using a 16-genotype probabilistic model
Stars: ✭ 26 (-71.74%)
Tiledb VcfEfficient variant-call data storage and retrieval library using the TileDB storage library.
Stars: ✭ 26 (-71.74%)
GvannoGeneric germline variant annotation pipeline
Stars: ✭ 23 (-75%)
Helmsmanhighly-efficient & lightweight mutation signature matrix aggregation
Stars: ✭ 19 (-79.35%)
HailScalable genomic data analysis.
Stars: ✭ 706 (+667.39%)
HtslibC library for high-throughput sequencing data formats
Stars: ✭ 529 (+475%)
VcardThis vCard PHP library can easily parse or generate/export vCards as .vcf
Stars: ✭ 333 (+261.96%)
PygenoPersonalized Genomics and Proteomics. Main diet: Ensembl, side dishes: SNPs
Stars: ✭ 261 (+183.7%)
Vcfannoannotate a VCF with other VCFs/BEDs/tabixed files
Stars: ✭ 259 (+181.52%)
VCF-kitVCF-kit: Assorted utilities for the variant call format
Stars: ✭ 94 (+2.17%)
23andme2vcfconvert your 23andme raw file to VCF | DEPRECATED, please see https://github.com/plantimals/2vcf
Stars: ✭ 91 (-1.09%)
OntologiesHome of the Genomic Feature and Variation Ontology (GFVO)
Stars: ✭ 16 (-82.61%)
TypeTEGenotyping of segregating mobile elements insertions
Stars: ✭ 15 (-83.7%)
vcf2gwasPython API for comprehensive GWAS analysis using GEMMA
Stars: ✭ 27 (-70.65%)
SVCollectorMethod to optimally select samples for validation and resequencing
Stars: ✭ 20 (-78.26%)
jannovarAnnotation of VCF variants with functional impact and from databases (executable+library)
Stars: ✭ 42 (-54.35%)
cutevariantA standalone and free application to explore genetics variations from VCF file
Stars: ✭ 61 (-33.7%)
vcf2tsvGenomic VCF to tab-separated values
Stars: ✭ 27 (-70.65%)
fucFrequently used commands in bioinformatics
Stars: ✭ 23 (-75%)
ilusA handy variant calling pipeline generator for whole genome re-sequencing (WGS) and whole exom sequencing data (WES) analysis. 一个简易且全面的 WGS/WES 分析流程生成器.
Stars: ✭ 64 (-30.43%)
cpsrCancer Predisposition Sequencing Reporter (CPSR)
Stars: ✭ 44 (-52.17%)
indelopefind large indels (in the blind spot between GATK/freebayes and SV callers)
Stars: ✭ 38 (-58.7%)
snpstools for reading, writing, merging, and remapping SNPs
Stars: ✭ 57 (-38.04%)
vcfstatsPowerful statistics for VCF files
Stars: ✭ 32 (-65.22%)
spark-vcfSpark VCF data source implementation for Dataframes
Stars: ✭ 15 (-83.7%)
SNPGenieProgram for estimating πN/πS, dN/dS, and other diversity measures from next-generation sequencing data
Stars: ✭ 81 (-11.96%)
2vcfconvert 23andme or Ancestry.com raw genotype calls into VCF format, with dbSNP annotations
Stars: ✭ 42 (-54.35%)
calcardbackupcalcardbackup: moved to https://codeberg.org/BernieO/calcardbackup
Stars: ✭ 67 (-27.17%)
vcf stuff📊Evaluating, filtering, comparing, and visualising VCF
Stars: ✭ 19 (-79.35%)
CuteVCFsimple viewer for variant call format using htslib
Stars: ✭ 30 (-67.39%)
laravel-vcardA fluent builder class for vCard files.
Stars: ✭ 29 (-68.48%)
vembranevembrane filters VCF records using python expressions
Stars: ✭ 46 (-50%)
Variants2NeoantigenA neoantigen calling pipeline begins from variants record file (MAF) (Not maintain now)
Stars: ✭ 27 (-70.65%)
csv2vcf🔧 Simple script in python to convert CSV files to VCF
Stars: ✭ 66 (-28.26%)
cljamA DNA Sequence Alignment/Map (SAM) library for Clojure
Stars: ✭ 85 (-7.61%)
Hap.pyHaplotype VCF comparison tools
Stars: ✭ 249 (+170.65%)
Snippy✂️ ⚡️ Rapid haploid variant calling and core genome alignment
Stars: ✭ 245 (+166.3%)
Cyvcf2cython + htslib == fast VCF and BCF processing
Stars: ✭ 243 (+164.13%)
Vcf2mafConvert a VCF into a MAF, where each variant is annotated to only one of all possible gene isoforms
Stars: ✭ 229 (+148.91%)
HtsjdkA Java API for high-throughput sequencing data (HTS) formats.
Stars: ✭ 220 (+139.13%)
SurvivorToolset for SV simulation, comparison and filtering
Stars: ✭ 180 (+95.65%)
PcgrPersonal Cancer Genome Reporter (PCGR)
Stars: ✭ 168 (+82.61%)
BiosyntaxSyntax highlighting for computational biology
Stars: ✭ 164 (+78.26%)
Vcf2phylipConvert SNPs in VCF format to PHYLIP, NEXUS, binary NEXUS, or FASTA alignments for phylogenetic analysis
Stars: ✭ 126 (+36.96%)
GenomicsA collection of scripts and notes related to genomics and bioinformatics
Stars: ✭ 101 (+9.78%)