proxy.golang.org "variant-calling" keyword
Top 4.4% on proxy.golang.org
2 versions - Latest release: about 2 months ago - 19 stars on GitHub
github.com/nbisweden/workshop-ngsintro v0.0.0-20260903221440-ecc46be2f11e removed
Workshop • Intro to Bioinformatics using NGS data • 5 days2 versions - Latest release: about 2 months ago - 19 stars on GitHub
Top 4.4% on proxy.golang.org
2 versions - Latest release: about 2 months ago - 19 stars on GitHub
github.com/NBISweden/workshop-ngsintro v0.0.0-20260905213029-ab70ea318ac4 removed
Workshop • Intro to Bioinformatics using NGS data • 5 days2 versions - Latest release: about 2 months ago - 19 stars on GitHub
Top 5.1% on proxy.golang.org
11 versions - Latest release: over 1 year ago - 138 stars on GitHub
github.com/andersen-lab/ivar v1.4.4
iVar is a computational package that contains functions broadly useful for viral amplicon-based s...11 versions - Latest release: over 1 year ago - 138 stars on GitHub
Top 1.0% on proxy.golang.org
30 versions - Latest release: over 6 years ago - 595 stars on GitHub
github.com/tseemann/snippy v4.6.0+incompatible
:scissors: :zap: Rapid haploid variant calling and core genome alignment30 versions - Latest release: over 6 years ago - 595 stars on GitHub
Top 5.1% on proxy.golang.org
1 version - Latest release: over 1 year ago - 16 stars on GitHub
github.com/nf-core/pacvar v1.0.0
Longread PacBio sequencing processing for WGS and PureTarget1 version - Latest release: over 1 year ago - 16 stars on GitHub
Top 6.7% on proxy.golang.org
1 version - Latest release: over 6 years ago - 49 stars on GitHub
github.com/nvidia/VariantWorks v0.1.0-rc1
Deep Learning based variant calling toolkit - https://clara-parabricks.github.io/VariantWorks/1 version - Latest release: over 6 years ago - 49 stars on GitHub
Top 6.7% on proxy.golang.org
1 version - Latest release: over 6 years ago - 49 stars on GitHub
github.com/nvidia/variantworks v0.1.0-rc1
Deep Learning based variant calling toolkit - https://clara-parabricks.github.io/VariantWorks/1 version - Latest release: over 6 years ago - 49 stars on GitHub
Top 5.1% on proxy.golang.org
105 versions - Latest release: 7 months ago - 59 stars on GitHub
github.com/clinical-genomics/balsamic v19.0.0+incompatible
Bioinformatic Analysis pipeLine for SomAtic Mutations In Cancer105 versions - Latest release: 7 months ago - 59 stars on GitHub
Top 5.1% on proxy.golang.org
105 versions - Latest release: 7 months ago - 59 stars on GitHub
github.com/Clinical-Genomics/BALSAMIC v19.0.0+incompatible
Bioinformatic Analysis pipeLine for SomAtic Mutations In Cancer105 versions - Latest release: 7 months ago - 59 stars on GitHub
Top 5.1% on proxy.golang.org
120 versions - Latest release: about 2 months ago - 933 stars on GitHub
github.com/TANGHAIBAO/jcvi v1.6.7
Python library to facilitate genome assembly, annotation, and comparative genomics120 versions - Latest release: about 2 months ago - 933 stars on GitHub
Top 5.1% on proxy.golang.org
120 versions - Latest release: about 2 months ago - 933 stars on GitHub
github.com/tanghaibao/jcvi v1.6.7
Python library to facilitate genome assembly, annotation, and comparative genomics120 versions - Latest release: about 2 months ago - 933 stars on GitHub
Top 5.1% on proxy.golang.org
105 versions - Latest release: 6 months ago - 59 stars on GitHub
github.com/Clinical-Genomics/balsamic v19.0.0+incompatible
Bioinformatic Analysis pipeLine for SomAtic Mutations In Cancer105 versions - Latest release: 6 months ago - 59 stars on GitHub
Top 5.1% on proxy.golang.org
3 versions - Latest release: over 4 years ago - 204 stars on GitHub
github.com/nanoporetech/megalodon v2.5.0+incompatible
Megalodon is a research command line tool to extract high accuracy modified base and sequence va...3 versions - Latest release: over 4 years ago - 204 stars on GitHub
Top 5.7% on proxy.golang.org
14 versions - Latest release: about 1 year ago - 281 stars on GitHub
github.com/suhrig/arriba v2.5.1+incompatible
Fast and accurate gene fusion detection from RNA-Seq data14 versions - Latest release: about 1 year ago - 281 stars on GitHub
Top 5.1% on proxy.golang.org
14 versions - Latest release: about 1 year ago - 282 stars on GitHub
github.com/Suhrig/arriba v2.5.1+incompatible
Fast and accurate gene fusion detection from RNA-Seq data14 versions - Latest release: about 1 year ago - 282 stars on GitHub
Top 4.5% on proxy.golang.org
2 versions - Latest release: 9 months ago - 614 stars on GitHub
github.com/nf-core/sarek v0.0.0-20260210112939-e9f175045340 removed
Analysis pipeline to detect germline or somatic variants (pre-processing, variant calling and ann...2 versions - Latest release: 9 months ago - 614 stars on GitHub
Top 5.1% on proxy.golang.org
123 versions - Latest release: 10 days ago - 197 stars on GitHub
github.com/broadinstitute/viral-ngs v3.0.27+incompatible
viral-ngs: command line tools and wrappers for processing raw viral genomic data123 versions - Latest release: 10 days ago - 197 stars on GitHub
Top 9.6% on proxy.golang.org
20 versions - Latest release: 8 months ago - 685 stars on GitHub
github.com/ekg/vcflib v1.0.15
C++ library and cmdline tools for parsing and manipulating VCF files with python and zig bindings20 versions - Latest release: 8 months ago - 685 stars on GitHub
Top 5.1% on proxy.golang.org
1 version - Latest release: over 1 year ago - 52 stars on GitHub
github.com/nf-core/variantbenchmarking v1.0.0
Pipeline to evaluate and validate the accuracy of variant calling methods in genomic research1 version - Latest release: over 1 year ago - 52 stars on GitHub
Top 4.3% on proxy.golang.org
1 version - Latest release: over 3 years ago - 126 stars on GitHub
github.com/nf-core/Raredisease v0.0.0-20230726085548-c371602095ff removed
Call and score variants from WGS/WES of rare disease patients.1 version - Latest release: over 3 years ago - 126 stars on GitHub
Top 4.7% on proxy.golang.org
13 versions - Latest release: over 4 years ago - 127 stars on GitHub
github.com/pacificbiosciences/ccs v6.4.0+incompatible
CCS: Generate Highly Accurate Single-Molecule Consensus Reads (HiFi Reads)13 versions - Latest release: over 4 years ago - 127 stars on GitHub
Top 4.6% on proxy.golang.org
16 versions - Latest release: over 6 years ago - 109 stars on GitHub
github.com/TileDB-Inc/TileDB-VCF v0.4.36
Efficient variant-call data storage and retrieval library using the TileDB storage library.16 versions - Latest release: over 6 years ago - 109 stars on GitHub
Top 4.8% on proxy.golang.org
15 versions - Latest release: over 6 years ago - 109 stars on GitHub
github.com/tiledb-inc/tiledb-vcf v0.4.36
Efficient variant-call data storage and retrieval library using the TileDB storage library.15 versions - Latest release: over 6 years ago - 109 stars on GitHub
Top 5.1% on proxy.golang.org
40 versions - Latest release: 5 months ago - 119 stars on GitHub
github.com/kcleal/dysgu v1.9.0
Toolkit for calling structural variants using short or long reads40 versions - Latest release: 5 months ago - 119 stars on GitHub
Top 5.1% on proxy.golang.org
40 versions - Latest release: 5 months ago - 119 stars on GitHub
github.com/kcleal/Dysgu v1.9.0
Toolkit for calling structural variants using short or long reads40 versions - Latest release: 5 months ago - 119 stars on GitHub
Top 5.1% on proxy.golang.org
12 versions - Latest release: almost 2 years ago - 28 stars on GitHub
github.com/sib-swiss/ngs-variants-training v2024.9.1+incompatible
GitHub for the SIB courses NGS - Genome variant analysis12 versions - Latest release: almost 2 years ago - 28 stars on GitHub
Top 5.1% on proxy.golang.org
12 versions - Latest release: almost 2 years ago - 28 stars on GitHub
github.com/sib-swiss/NGS-variants-training v2024.9.1+incompatible
GitHub for the SIB courses NGS - Genome variant analysis12 versions - Latest release: almost 2 years ago - 28 stars on GitHub
Top 5.1% on proxy.golang.org
3 versions - Latest release: 7 months ago - 7 stars on GitHub
github.com/MPUSP/snakemake-ont-bacterial-variants v1.1.1
A Snakemake workflow for the identification of variants in bacterial genomes using nanopore long-...3 versions - Latest release: 7 months ago - 7 stars on GitHub
Top 5.1% on proxy.golang.org
3 versions - Latest release: 7 months ago - 7 stars on GitHub
github.com/mpusp/snakemake-ont-bacterial-variants v1.1.1
A Snakemake workflow for the identification of variants in bacterial genomes using nanopore long-...3 versions - Latest release: 7 months ago - 7 stars on GitHub
Top 5.1% on proxy.golang.org
61 versions - Latest release: 18 days ago - 151 stars on GitHub
github.com/sequana/sequana v0.25.0
Sequana: a set of Snakemake NGS pipelines61 versions - Latest release: 18 days ago - 151 stars on GitHub
Top 5.1% on proxy.golang.org
20 versions - Latest release: about 2 months ago - 392 stars on GitHub
github.com/HKU-BAL/Clair3 v2.0.3+incompatible
Clair3 - Symphonizing pileup and full-alignment for deep learning-based long-read variant calling20 versions - Latest release: about 2 months ago - 392 stars on GitHub
Top 5.1% on proxy.golang.org
20 versions - Latest release: about 2 months ago - 392 stars on GitHub
github.com/hku-bal/clair3 v2.0.3+incompatible
Clair3 - Symphonizing pileup and full-alignment for deep learning-based long-read variant calling20 versions - Latest release: about 2 months ago - 392 stars on GitHub
Top 9.6% on proxy.golang.org
32 versions - Latest release: over 5 years ago - 327 stars on GitHub
github.com/luntergroup/octopus v0.7.4
Bayesian haplotype-based mutation calling32 versions - Latest release: over 5 years ago - 327 stars on GitHub
Top 9.6% on proxy.golang.org
20 versions - Latest release: 8 months ago - 686 stars on GitHub
github.com/vcflib/vcflib v1.0.15
C++ library and cmdline tools for parsing and manipulating VCF files with python and zig bindings20 versions - Latest release: 8 months ago - 686 stars on GitHub
Top 5.6% on proxy.golang.org
6 versions - Latest release: about 6 years ago - 62 stars on GitHub
github.com/czbiohub/cerebra v1.2.0
A tool for fast and accurate summarizing of variant calling format (VCF) files6 versions - Latest release: about 6 years ago - 62 stars on GitHub
Top 5.1% on proxy.golang.org
15 versions - Latest release: 2 months ago - 1 stars on GitHub
github.com/MPUSP/snakemake-simple-mapping v1.8.0
A Snakemake workflow for the mapping of reads to reference genomes, minimalistic and simple.15 versions - Latest release: 2 months ago - 1 stars on GitHub
Top 5.1% on proxy.golang.org
15 versions - Latest release: 2 months ago - 1 stars on GitHub
github.com/mpusp/snakemake-simple-mapping v1.8.0
A Snakemake workflow for the mapping of reads to reference genomes, minimalistic and simple.15 versions - Latest release: 2 months ago - 1 stars on GitHub
Top 5.0% on proxy.golang.org
24 versions - Latest release: over 1 year ago - 119 stars on GitHub
github.com/moiexpositoalonsolab/grenepipe v0.15.0
A flexible, scalable, and reproducible pipeline to automate variant calling from raw sequence rea...24 versions - Latest release: over 1 year ago - 119 stars on GitHub
Top 5.6% on proxy.golang.org
1 version - Latest release: about 8 years ago - 137 stars on GitHub
github.com/crg-cnag/callings-nf v1.0.0
GATK RNA-Seq Variant Calling in Nextflow1 version - Latest release: about 8 years ago - 137 stars on GitHub
Top 5.6% on proxy.golang.org
1 version - Latest release: about 8 years ago - 137 stars on GitHub
github.com/CRG-CNAG/CalliNGS-NF v1.0.0
GATK RNA-Seq Variant Calling in Nextflow1 version - Latest release: about 8 years ago - 137 stars on GitHub
Top 5.1% on proxy.golang.org
1 version - Latest release: about 8 years ago - 137 stars on GitHub
github.com/CRG-CNAG/CalLINGS-NF v1.0.0
GATK RNA-Seq Variant Calling in Nextflow1 version - Latest release: about 8 years ago - 137 stars on GitHub
Related Keywords
genomics
25
bioinformatics
19
nextflow
7
ngs
7
snakemake
6
rna-seq
6
workflow
6
gatk
5
pacbio
5
pipeline
4
nf-core
4
structural-variation
4
nanopore
4
deep-learning
4
ngs-analysis
4
genome-sequencing
3
somatic-mutations
3
conda
3
cancer
3
illumina
3
snakemake-workflow
3
snakemake-workflows
3
next-generation-sequencing
3
long-read
3
vcf
3
python
3
polishing
2
gene-fusions
2
star
2
virus-integration
2
synteny
2
sequence-alignments
2
rnaseq
2
genetic-maps
2
comparative-genomics
2
blast
2
assembly
2
allmaps
2
unix-shell
2
paired-end
2
structural
2
gene-fusion
2
fusion-genes
2
variant
2
structural-variants
2
bioinformatics-pipeline
2
fusion-gene
2
singularity
2
tutorial
2
course
2
training
2
teaching
2
ont-data
2
ont-models
2
long-reads
2
computational-biology
2
bowtie2
2
variant-detection
2
bwa-mem2
2
tiledb-api
2
tiledb
2
genotyping
2
haplotypecaller
2
vcf-manipulation
2
spark
2
gwas
2
data-science
2
wgs
2
mapping
2
star-alignment
2
wes
1
variant-annotation
1
snv
1
rare-disease
1
diagnostics
1
annotation
1
containers
1
gatk4
1
benchmark
1
small-variants
1
amplicon-sequencing
1
bam
1
docker
1
fastq
1
genome
1
genome-assembly
1
variant-annotations
1
viral
1
viral-ngs
1
puretarget
1
alignment
1
ancient-dna
1
pre-processing
1
reproducible-research
1
somatic
1
scrna-seq
1
mutations
1
target-panels
1
whole-exome-sequencing
1
whole-genome-sequencing
1