ChillarAnand / fadapaLinks
FAstqc DAta PArser - A minimal parser to parse FastQC output data.
☆16Updated 9 years ago
Alternatives and similar repositories for fadapa
Users that are interested in fadapa are comparing it to the libraries listed below
Sorting:
- ☆37Updated 5 years ago
- reference free variant assembly☆34Updated 2 years ago
- prioritize effects of variant annotations from VEP, SnpEff, et al.☆34Updated 8 months ago
- SMBL - SnakeMake Bioinformatics Library. Automatic installation of bioinformatics software in your SnakeMake pipelines.☆23Updated 8 years ago
- Visualise interstrain recombination from environmental samples.☆26Updated 6 years ago
- Homebrew formulae for bioinformatics software only available for Linux☆27Updated 6 years ago
- Stupid Simple Structural Variant View☆25Updated 8 years ago
- sort genomic data☆36Updated 5 years ago
- create a gemini-compatible database from a VCF☆56Updated 4 years ago
- Qtip: a tandem simulation approach for accurately predicting read alignment mapping qualities☆25Updated 5 years ago
- Ococo: the first online variant and consensus caller. Call genomic consensus directly from an unsorted SAM/BAM stream.☆47Updated 6 years ago
- BigWig manpulation tools using libBigWig and htslib☆29Updated last year
- Public Health England SNP calling pipeline.☆37Updated 6 years ago
- DNA assembler developed on FER (Croatia), RBI (Croatia) and GIS (Singapore)☆18Updated 9 years ago
- Please see https://github.com/chanzuckerberg/czid-workflows for the latest version of CZ ID workflows.☆27Updated 3 years ago
- Snakemake library for bioinformatics programs, with a focus on next-generation sequencing☆22Updated 9 years ago
- Docker images of bioinformatics software☆21Updated 8 years ago
- Rapid competitive read demulitplexer. Made with tries.☆23Updated 3 months ago
- Mapping-free variant caller for short-read Illumina data☆19Updated 5 years ago
- ☆19Updated 8 years ago
- FAST: Fast Analysis of Sequences Toolbox☆31Updated 5 years ago
- robust matching of small variant datasets using flexible scoring schemes☆11Updated 5 years ago
- Browser based application for viewing bam alignments☆56Updated 8 years ago
- Color DNA/RNA bases in terminal output☆21Updated 8 years ago
- Nanopore desc☆18Updated 9 years ago
- Reference-free variant discovery in large eukaryotic genomes☆41Updated 4 years ago
- Pipeline for poreathon☆14Updated 10 years ago
- conda recipes for genomic data☆85Updated 4 years ago
- Software for detecting transposable element insertions from next-generation sequencing data☆14Updated 4 years ago
- Course material for the de novo assembly part of the INF-BIO9120 course at Univ. of Oslo Fall 2013☆37Updated 11 years ago