bcbc-group / CyVerese_SNP_calling_webinarLinks
☆10Updated 4 years ago
Alternatives and similar repositories for CyVerese_SNP_calling_webinar
Users that are interested in CyVerese_SNP_calling_webinar are comparing it to the libraries listed below
Sorting:
- Evolutionary Transcriptomics with R☆45Updated this week
- Pipeline to take VCF through to Selection Analysis.☆58Updated 2 years ago
- A command line tool to compute mapping statistics from a BAM file☆24Updated 3 years ago
- A set of R functions that help faciliate a lot of tedious processing☆18Updated 6 years ago
- ☆17Updated 4 years ago
- A set of workflows written in Nextflow for Genome Annotation.☆45Updated last year
- Splice junction analysis and filtering from BAM files☆40Updated 3 years ago
- Adapters for trimming☆30Updated 6 years ago
- Integrative analysis of structural variations.☆40Updated last year
- Snakemake workflow for Illumina RNA-sequencing experiments - extract population genomic signals from RNA-Seq data☆18Updated 4 months ago
- Relative Abundance of Transcripts: An R package for the detection of Differential Transcript isoform Usage.☆34Updated 3 years ago
- An efficient way to guess the library type of your RNA-Seq data.☆31Updated 2 years ago
- UNDER DEVELOPMENT--- Analysis of long non-coding RNAs from RNA-seq datasets☆34Updated 4 months ago
- ☆30Updated 2 months ago
- Genome wide orthology inference and dNdS estimation☆95Updated last year
- ☆11Updated 3 years ago
- QUILT: Low coverage whole genome sequence imputation with large reference panels☆65Updated 3 weeks ago
- ☆9Updated 7 years ago
- An R framework for phylostratigraphy☆32Updated this week
- A framework to build Software As A Service (SaaS) platforms for Nextflow pipelines.☆17Updated this week
- NGSNGS: Next generation simulator for next generation sequencing data☆53Updated 8 months ago
- Nanopore data analysis in R☆40Updated 2 years ago
- A program for the Maximum-likelihood analysis of population genomic data.☆29Updated 4 years ago
- ☆19Updated last year
- BigWig and BAM utilities☆97Updated last year
- DensityMap is perl tool for the visualization of features density along chromosomes☆18Updated 3 years ago
- A catalogue of available long read sequencing data analysis tools☆78Updated 5 months ago
- an R/Shiny application for interactive creation of non-circular plots of whole genomes☆45Updated 2 months ago
- Code for the Brassica oleracea/rapa/napus genomic comparison☆16Updated 4 years ago
- Flexible Genotyping of Polyploids using Next Generation Sequencing Data☆29Updated 9 months ago