vsbuffalo / bioawk-tutorialLinks
☆44Updated 12 years ago
Alternatives and similar repositories for bioawk-tutorial
Users that are interested in bioawk-tutorial are comparing it to the libraries listed below
Sorting:
- Software for clustering de novo assembled transcripts and counting overlapping reads☆76Updated 3 years ago
- A collection of scripts for processing fastq files in ways to improve de novo transcriptome assemblies, and for evaluating those assembli…☆51Updated last year
- web documentation for Trinotate☆48Updated 2 years ago
- A snakemake pipeline for SV analysis from nanopore genome sequencing☆52Updated 5 years ago
- Pipeline to take VCF through to Selection Analysis.☆58Updated 3 years ago
- a bash pipeline for RAD sequencing☆55Updated 10 months ago
- Toolkit for processing TAB-delimited format☆62Updated last year
- Miscellaneous Bioinformatics scripts etc mostly in Python☆45Updated 2 weeks ago
- Building SuperTranscripts: A linear representation of transcriptome data☆68Updated 4 years ago
- 10x Genomics Linked-Read Diploid De Novo Assembler☆65Updated 7 years ago
- Rank-based Gene Ontology analysis of gene expression data☆43Updated 3 years ago
- Tools for working with second gen assemblies, fasta sequences, etc☆93Updated 9 years ago
- Annocript is a pipeline for the annotation of de-novo generated transcriptomes. It executes BLAST analysis with UniProt, NCBI Conserved …☆56Updated 5 years ago
- Quickly calculate and visualize sequence coverage in alignment files☆101Updated 6 years ago
- Nanopore data analysis in R☆40Updated 2 years ago
- A set of functions to visualise genotypes based on a VCF☆87Updated 3 years ago
- ☆78Updated 11 years ago
- materials for the RNA-Seq workshop on Trinity and Tuxedo, covering de novo and genome-guided transcript assembly and downstream analysis.☆48Updated 9 years ago
- ☆35Updated 2 years ago
- Genome Annotation Without Nightmares☆46Updated 10 months ago
- Bioinformatics tools for dealing with Multiple Alignment Format (MAF) files.☆109Updated 3 years ago
- Julia package powering VIVA, our tool for visualization of genomic variation data. Manual:☆86Updated 2 years ago
- A program for the Maximum-likelihood analysis of population genomic data.☆30Updated 4 years ago
- A catalogue of available long read sequencing data analysis tools☆83Updated 2 months ago
- Repository of common bioinformatics scripts☆39Updated 4 years ago
- ☆63Updated 5 years ago
- A set of workflows written in Nextflow for Genome Annotation.☆46Updated last year
- Pipelines and tools for the processing of ancient and modern HTS data.☆48Updated last month
- LaTeX and associated files for lecture notes used in EEB 5348 at the University of Connecticut☆35Updated 2 years ago
- PrimerTree: Visually Assessing the Specificity and Informativeness of Primer Pairs☆52Updated last month