goeckslab / isoseq-browserLinks
☆13Updated 8 years ago
Alternatives and similar repositories for isoseq-browser
Users that are interested in isoseq-browser are comparing it to the libraries listed below
Sorting:
- Making Snakemake workflows into full-fledged command line tools since 1999.☆51Updated 7 years ago
- Simplify snpEff annotations for interesting cases☆22Updated 6 years ago
- BigWig manpulation tools using libBigWig and htslib☆29Updated last year
- Samwell: a python package for using genomic files... well☆20Updated 3 years ago
- Demonstrating best practices for bioinformatics command line tools☆26Updated 5 years ago
- Manuscript describing ChronQC is now available online in Bioinformatics☆18Updated 6 years ago
- A web based tool to manage and automate the processing of publicly available datasets.☆39Updated 4 years ago
- Portable WDL workflows for IDseq production pipelines☆32Updated 3 years ago
- Malleable All-seeing Journal Of Research Artifacts☆35Updated 2 years ago
- CheckQC inspects the content of an Illumina runfolder and determines if it passes a set of quality criteria☆28Updated 3 months ago
- conda recipes for genomic data☆84Updated 4 years ago
- A fast, easy way to present complex bioinformatics pipelines to biologists☆11Updated 7 years ago
- Nextflow workshop 2018 -- Training pages -> https://nextflow-io.github.io/nf-hack18/☆18Updated 6 years ago
- Snakemake skeleton - Build workflows with Snakemake☆19Updated last year
- Precursor to SnakeChunks, see https://github.com/SnakeChunks/SnakeChunks. This project has moved and will no longer be edited here.☆11Updated 8 years ago
- Chanjo provides a better way to analyze coverage data in clinical sequencing.☆51Updated 9 months ago
- What's The Function of these genes?☆22Updated 8 years ago
- ☆18Updated 8 years ago
- Prepare Sailfish and Salmon output for downstream analysis☆42Updated 6 years ago
- The command-line interface to GGD☆42Updated 2 years ago
- A Framework to call Structural Variants from NGS based datasets☆22Updated 7 years ago
- Please consider using/contributing to https://github.com/nf-core/sarek☆41Updated 4 years ago
- Accurate, Lightweight Clustering of de novo Transcriptomes using Fragment Equivalence Classes☆31Updated last year
- seqcover allows users to view coverage for hundreds of genes and dozens of samples☆52Updated 4 years ago
- 🍶 Genome assembly with short sequence reads☆25Updated last year
- a Shiny/R application to view and annotate copy number variations☆28Updated 2 years ago
- full taxonomer cython repository☆22Updated 5 years ago
- TreeGrafter is a new software tool for annotating uncharacterized protein sequences, using annotated phylogenetic trees.☆11Updated 2 months ago
- prioritize effects of variant annotations from VEP, SnpEff, et al.☆34Updated 9 months ago
- Ximmer is a system for CNV calling on exome and targeted genomic sequencing☆19Updated 2 weeks ago