cccnrc / plot-VCFLinks
visual analysis of your VCF files
☆38Updated 3 years ago
Alternatives and similar repositories for plot-VCF
Users that are interested in plot-VCF are comparing it to the libraries listed below
Sorting:
- gatk4 RNA variant calling pipeline☆56Updated 2 weeks ago
- A Nextflow Genome-Wide Association Study (GWAS) Pipeline☆36Updated 6 months ago
- GFF3sort: A Perl Script to sort gff3 files and produce suitable results for tabix tools☆51Updated 5 years ago
- Pipeline to evaluate and validate the accuracy of variant calling methods in genomic research☆36Updated 3 weeks ago
- Splice junction analysis and filtering from BAM files☆42Updated 3 years ago
- A nextflow pipeline to perform state-of-the-art genome-wide association studies.☆76Updated 2 months ago
- for visual evaluation of read support for structural variation☆55Updated last year
- A catalogue of available long read sequencing data analysis tools☆83Updated 3 months ago
- Rapid analysis and visualisation for bulk RNA-seq, psuedo-bulk RNA-seq, GeoMx and Proteomic datasets.☆30Updated last year
- For biological deep sequencing data. Decompose a UCSC knownGenes/Ensembl GTF file into transcript regions (i.e. exons, introns, UTRs and…☆36Updated 2 years ago
- POSTRE: Prediction Of STRuctural variant Effects☆28Updated 10 months ago
- my bin directory☆45Updated 3 months ago
- An efficient way to guess the library type of your RNA-Seq data.☆33Updated 3 years ago
- A python parser to simplify and build the VCF (Variant Call Format).☆49Updated last year
- perSVade: personalized Structural Variation detection☆40Updated 3 months ago
- My bioinfo toolbox☆50Updated 10 months ago
- python plotly Circos from VCF☆40Updated last year
- The Zavolab Automated RNA-seq Pipeline☆36Updated 5 months ago
- A software for calculating telomere length☆72Updated 7 years ago
- course about NGS data processing: genomics and transcriptomics☆33Updated 4 years ago
- Workflow to prepare high accuracy single molecule consensus sequences from amplicon data using unique molecular identifiers☆35Updated last year
- Analysis of TE contribution to features (transcripts or simple features). Includes utils to test enrichment.☆29Updated 6 years ago
- An R package for estimating poly(A)-tail lengths in Oxford Nanopore RNA and DNA reads.☆55Updated last year
- Evolutionary Transcriptomics with R☆48Updated last month
- Flexible and efficient parsing, interpreting and editing of sequencing reads☆44Updated 3 weeks ago
- Powerful statistics for VCF files☆73Updated last month
- ☆35Updated 2 years ago
- A tool for accurately detecting actively translating ORFs from Ribo-seq data☆39Updated 11 months ago
- ☆27Updated last year
- A tutorial on structural variant calling for short read sequencing data☆38Updated last year