homologus / Pandoras-Toolbox-for-BioinformaticsLinks
A collection of well-known bioinformatics programs.
☆25Updated 10 years ago
Alternatives and similar repositories for Pandoras-Toolbox-for-Bioinformatics
Users that are interested in Pandoras-Toolbox-for-Bioinformatics are comparing it to the libraries listed below
Sorting:
- Chanjo provides a better way to analyze coverage data in clinical sequencing.☆50Updated 5 months ago
- Biological Graphic tool in Python☆34Updated 5 years ago
- Tools for next-generation sequencing analysis☆88Updated 5 years ago
- Stupid Simple Structural Variant View☆25Updated 8 years ago
- A tool to benchmark mappers and different parameters within minutes☆44Updated 5 years ago
- Scalable RNA-seq analysis☆73Updated 4 years ago
- Browser based application for viewing bam alignments☆56Updated 8 years ago
- Visualise interstrain recombination from environmental samples.☆26Updated 6 years ago
- conda recipes for genomic data☆85Updated 3 years ago
- prioritize effects of variant annotations from VEP, SnpEff, et al.☆34Updated 5 months ago
- CLAMMS is a scalable tool for detecting common and rare copy number variants from whole-exome sequencing data.☆29Updated 4 years ago
- An awk-like VCF parser☆56Updated last year
- Run Picard on BAM files and collate 90 metrics into one file.☆41Updated 7 years ago
- Tools for bam file processing☆55Updated 10 years ago
- ☆78Updated 11 years ago
- Variant caller GUI + genetic disease analysis☆22Updated 5 years ago
- The gkno launcher for executing tools or pipelines☆31Updated 8 years ago
- Preprocessing tools for unique molecular index (UMI) sequencing reads☆31Updated 2 years ago
- create a gemini-compatible database from a VCF☆56Updated 4 years ago
- A method to identify structural variation from sequencing data in target regions☆31Updated 4 years ago
- Curated collection of open-source bioinformatics tools☆28Updated 6 years ago
- QC3, a quality control tool designed for DNA sequencing data for raw data, alignment, and variant calling.☆32Updated 9 years ago
- Response to blog post about Salmon☆37Updated 7 years ago
- ☆30Updated 8 years ago
- What's The Function of these genes?☆22Updated 8 years ago
- ☆82Updated 3 years ago
- High-performance error correction for Illumina resequencing data☆71Updated 9 years ago
- Tools to handle reads sequenced with unique molecular identifiers (UMIs).☆30Updated 7 years ago
- a wee tool for random access into BGZF files.