epi2me-labs / ezchartsLinks
☆22Updated 3 weeks ago
Alternatives and similar repositories for ezcharts
Users that are interested in ezcharts are comparing it to the libraries listed below
Sorting:
- a minimal, scriptable genome browser for python☆51Updated 10 months ago
- Read, parse and operate different multiple input file formats with OpenVariant☆14Updated 5 months ago
- Python bindings for the TaxonKit library☆40Updated 4 months ago
- A genome browser in your Jupyter notebook☆31Updated 5 months ago
- Quality of life improvements for Bioinformatics in Python.☆31Updated 3 weeks ago
- Blazing-Fast Bioinformatic Operations on Python DataFrames☆98Updated this week
- Variant-aware CRISPR off-target nomination☆22Updated this week
- A python package and a set of shell commands to handle GTF files☆49Updated last year
- Fast sequencing data quality metrics☆28Updated last month
- BigSeqKit: a parallel Big Data toolkit to process FASTA and FASTQ files at scale☆56Updated 2 years ago
- vembrane filters VCF records using python expressions☆65Updated last month
- Gapless, reference-quality Southern Han Chinese genome assembly and annotation☆12Updated 3 years ago
- The script presents a simple way to visualize features on human chromosome ideograms☆42Updated 5 months ago
- This tools counts the number of specific k-mers within sequence data. The counts can then be compare to other counts to determine to comp…☆30Updated 11 months ago
- 🧬 High-performance VCF file parser and reformatter with VEP annotation support. Converts complex VCF files to analyzable TSV format …☆41Updated 2 months ago
- Blazing fast toolkit to work with .hic and .cool files☆41Updated this week
- Location of public benchmarking; primarily final results☆18Updated 8 months ago
- POSTRE: Prediction Of STRuctural variant Effects☆28Updated 8 months ago
- Ultra-fast 5' and 3' demultiplexer☆28Updated last year
- Processing and plotting tools for genomics data☆21Updated 2 months ago
- Python bindings to spoa☆21Updated 2 months ago
- (WIP) best-practices workflow for rare disease☆62Updated last year
- A tool for simulating random mutations in any genome☆42Updated last year
- A Python package for fast operations on 1-dimensional genomic signal tracks☆23Updated 5 years ago
- A python tool box for fast and accurate quality control, conversion and alignment of nanopore sequencing data☆20Updated 3 years ago
- ☆19Updated last week
- What is true, thank you, ernestly. A large variant benchmarking tool analogous to hap.py for small variants.☆33Updated 2 years ago
- A tool for de novo clustering of long transcriptomic reads☆15Updated 3 years ago
- Fast FASTQ sample demultiplexing in Rust.☆66Updated last week
- Tool package to perform in-silico CRISPR analysis and assessment☆32Updated last month