MonashBioinformaticsPlatform / RNAsik-pipeLinks
RNAsik - more than just a pipeline
☆13Updated last year
Alternatives and similar repositories for RNAsik-pipe
Users that are interested in RNAsik-pipe are comparing it to the libraries listed below
Sorting:
- Homebrew formulae for bioinformatics software only available for Linux☆27Updated 6 years ago
- ☆18Updated 8 years ago
- ☆25Updated 4 years ago
- Qtip: a tandem simulation approach for accurately predicting read alignment mapping qualities☆25Updated 5 years ago
- Prepare Sailfish and Salmon output for downstream analysis☆42Updated 6 years ago
- Making Snakemake workflows into full-fledged command line tools since 1999.☆51Updated 7 years ago
- Snakemake skeleton - Build workflows with Snakemake☆19Updated last year
- Analysis of RNAseq data from (host-associated) microbial mixtures☆12Updated 5 years ago
- Workflows I find helpful for fungal genome annotation☆21Updated 2 years ago
- A pipeline for preprocessing NGS data from Illumina, Nanopore and PacBio technologies☆35Updated last year
- Visualise interstrain recombination from environmental samples.☆26Updated 6 years ago
- ☆10Updated 13 years ago
- SMBL - SnakeMake Bioinformatics Library. Automatic installation of bioinformatics software in your SnakeMake pipelines.☆23Updated 8 years ago
- What's The Function of these genes?☆22Updated 8 years ago
- R Interface to the NCBI SRA metadata☆23Updated 6 years ago
- Metagenomic profiling and phylogenetic distances via common kmers☆42Updated 4 years ago
- prioritize effects of variant annotations from VEP, SnpEff, et al.☆34Updated 9 months ago
- Tool for quick offline batch conversion of Genbank IDs or accessions to taxonomy strings☆14Updated last year
- Accurate, Lightweight Clustering of de novo Transcriptomes using Fragment Equivalence Classes☆31Updated last year
- A program for fast and accurate genome-guided transcripts reconstruction and quantification from RNA-seq (Supporting Pacbio single-end)☆24Updated 4 years ago
- BigWig manpulation tools using libBigWig and htslib☆29Updated last year
- Assembly and intrahost / low-frequency variant calling for viral samples☆15Updated 5 years ago
- Nextflow workshop 2018 -- Training pages -> https://nextflow-io.github.io/nf-hack18/☆18Updated 6 years ago
- variant discovery and annotation using GATK and Ensembl☆17Updated 12 years ago
- UMCU Genetics Nextflow modules☆28Updated 10 months ago
- VIRULIGN: fast codon-correct alignment and annotation of viral genomes☆35Updated 4 years ago
- Malleable All-seeing Journal Of Research Artifacts☆35Updated 2 years ago
- This repository has been archived, currently maintained version is at https://github.com/iii-companion/companion☆21Updated 4 years ago
- Please see https://github.com/chanzuckerberg/czid-workflows for the latest version of CZ ID workflows.☆27Updated 3 years ago
- programs and scripts, mainly python, for analyses related to nucleic or protein sequences☆24Updated last month