listen-now / listen-now-desktopView external linksLinks
listen-now的跨平台桌面客户端，基于Electron开发。
☆28Oct 9, 2018Updated 7 years ago
Alternatives and similar repositories for listen-now-desktop
Users that are interested in listen-now-desktop are comparing it to the libraries listed below
Sorting:
- a little react implementation☆10May 5, 2020Updated 5 years ago
- ☆12Apr 26, 2020Updated 5 years ago
- A local realigner around InDels for MethylSeq data☆12Apr 28, 2016Updated 9 years ago
- Pipeline in place at the UGI for DNA level analysis☆11Aug 29, 2016Updated 9 years ago
- Divine: Prioritizing Genes for Rare Mendelian Disease in Whole Exome Sequencing Data☆13Apr 18, 2019Updated 6 years ago
- visualization tools for exon/junction coverage☆11Dec 30, 2019Updated 6 years ago
- Translocator: local realignment and global remapping enabling accurate translocation detection using single-molecule sequencing long read…☆12Jan 22, 2020Updated 6 years ago
- A protocol to estimate global ancestry starting from raw Illumina data☆11Oct 16, 2019Updated 6 years ago
- Fast, accurate and simple to use command line tool for variant detection in NGS data.☆12Sep 3, 2019Updated 6 years ago
- ☆11Dec 9, 2022Updated 3 years ago
- 使用javascript实现的类似yacc/bison的语法解析器的生成器☆17Nov 20, 2017Updated 8 years ago
- Rails application for storing and parsing clinical exome VCF files. Gene annotations can be retrieved via Biomart integration from Ensemb…☆10May 7, 2017Updated 8 years ago
- Automated ACMG/AMP classification for human variants associated with congenital hearing loss☆11May 14, 2025Updated 9 months ago
- CardiacProfileR: An R package for extraction and visualisation of heart rate profiles from wearable fitness trackers☆12Jun 10, 2018Updated 7 years ago
- Code to reproduce "Detecting liver cancer using cell-free DNA fragmentomes☆11Nov 18, 2022Updated 3 years ago
- Implementation of eBWT using Prefix-free parse (PFP)☆14Jul 14, 2025Updated 7 months ago
- ☆13Jul 3, 2024Updated last year
- Add functional variant annotation to MAF file☆11Nov 20, 2024Updated last year
- ☆13Apr 18, 2022Updated 3 years ago
- Interactive table from gemini output☆10Mar 5, 2019Updated 6 years ago
- Header-only, gzread-like reader for gzip, bz2, and xz.☆11Aug 8, 2018Updated 7 years ago
- 🔨 a tiny but powerful javascript library that performs client-side routing, templating, and REST API communication to help you get your …☆14Oct 23, 2016Updated 9 years ago
- Pan gGnome Viewer☆10Jul 10, 2025Updated 7 months ago
- Fast, efficient, lossless compression of fastq files☆14Jan 4, 2021Updated 5 years ago
- Pipeline for generating RNAseq-based cancer patient reports☆11Feb 4, 2026Updated last week
- ☆11Jun 14, 2023Updated 2 years ago
- A nextflow pipeline for calling and annotating small germline variants from short DNA reads for WES and WGS data☆13Updated this week
- ☆10Jun 9, 2020Updated 5 years ago
- A tool to analyze telomeric reads from WGS or telobait-capture long-read sequencing data☆10Oct 1, 2024Updated last year
- Open Targets Genetics UI☆15Jan 31, 2025Updated last year
- A tool to examine duplicate read characteristics in a BAM file☆12Dec 8, 2017Updated 8 years ago
- A nextflow pipeline for calling exome CNVs☆13Feb 9, 2026Updated last week
- ☆11Apr 3, 2023Updated 2 years ago
- A tool for detecting CNVs from WGS data☆11Jul 9, 2020Updated 5 years ago
- ☆11Aug 6, 2019Updated 6 years ago
- Enabling differential allele-specific analysis☆11Dec 28, 2024Updated last year
- Web application for clinical pharmacogenomic interpretation☆10Mar 3, 2017Updated 8 years ago
- Run-length compressed BWT with LZ77 sampled suffix array☆10Apr 25, 2022Updated 3 years ago
- Code used to process and analyze structural variants and short tandem repeat variants profiled in 719 deeply sequenced whole genomes as p…☆11Jun 25, 2019Updated 6 years ago