A lightweight Python graphing API for genomic features
☆15Jul 8, 2022Updated 3 years ago
Alternatives and similar repositories for genome-browser
Users that are interested in genome-browser are comparing it to the libraries listed below. We may earn a commission when you buy through links labeled 'Ad' on this page.
Sorting:
- probability of mendelian error in trios.☆11Jan 27, 2016Updated 10 years ago
- use the noise☆15Apr 15, 2020Updated 5 years ago
- Gene lists related to cancer immunotherapy☆14Sep 11, 2024Updated last year
- sort genomic data☆36Nov 7, 2025Updated 4 months ago
- Stupid Simple (ba)Sh Testing - A functional software testing framwork☆23Nov 8, 2023Updated 2 years ago
- A JBrowse plugin for plotting multiple bigwig subtracks☆12Feb 13, 2022Updated 4 years ago
- ☆12Jun 29, 2018Updated 7 years ago
- Making diploid assembly becomes common practice for genomic study☆30Oct 2, 2017Updated 8 years ago
- Stupid Simple Structural Variant View☆25Nov 21, 2016Updated 9 years ago
- SIMD-parallel BLAST X-drop DP on sequence graphs☆24May 30, 2024Updated last year
- Readability enhancement tool for bioinformatics data file format☆29Jan 9, 2020Updated 6 years ago
- find large indels (in the blind spot between GATK/freebayes and SV callers)☆39Dec 3, 2017Updated 8 years ago
- Numerical Encoding for Human Genetic Variants☆42Jun 8, 2023Updated 2 years ago
- Transfer HiFi read mappings from their own assembly contigs to a standard reference☆38Dec 30, 2025Updated 2 months ago
- pathoscore evaluates variant pathogenicity tools and scores.☆22Mar 25, 2022Updated 3 years ago
- A new web-based HTML5 genome browser. Genome Maps can also browse BAM and VCFs files among other formats.☆27Sep 24, 2013Updated 12 years ago
- A flexible python program for generating figures from regions of the genome.☆13Apr 6, 2019Updated 6 years ago
- A wrapper to Heng Li's kseq/readfq, an efficient FastQ/Fasta parser☆15Jun 28, 2023Updated 2 years ago
- a bioinformatics tool for simulating single-cell genome sequencing data☆10Dec 19, 2019Updated 6 years ago
- A read alignment visualization library for long reads☆10Aug 6, 2022Updated 3 years ago
- Python scripts for Exploratory Data Analysis of Pacific Biosciences sequence data☆18Aug 13, 2014Updated 11 years ago
- Small general purpose library for C and Python with focus on bioinformatics.☆31Sep 15, 2022Updated 3 years ago
- a novel next-generation sequencing simulator using position and genomic contexts based error profiles☆13Dec 18, 2020Updated 5 years ago
- Simply feedforward neural network☆19Oct 4, 2016Updated 9 years ago
- The python binding for D4 format☆16Oct 22, 2021Updated 4 years ago
- horizontal pileup☆16Nov 11, 2022Updated 3 years ago
- Dot2dot: Accurate Whole-Genome Tandem Repeats Discovery☆11Oct 5, 2022Updated 3 years ago
- UCSC Genome Browser Docker Image☆17May 12, 2022Updated 3 years ago
- 🐍 Deep Learning Type Inference of Python Function Signatures using their Natural Language Context☆17May 3, 2024Updated last year
- Genome browser to visualize and analyze genomic data☆13Nov 22, 2021Updated 4 years ago
- Sweep-line algorithm for genomic features. Detect overlaps on large files w/ minimal memory.☆10Sep 13, 2011Updated 14 years ago
- vcf file manipulation☆22Jul 9, 2015Updated 10 years ago
- Python library for talking to Apollo API