Isaac Genome Alignment Software
☆36Apr 7, 2015Updated 10 years ago
Alternatives and similar repositories for isaac_aligner
Users that are interested in isaac_aligner are comparing it to the libraries listed below
Sorting:
- This project is deprecated, please see strelka2 at https://github.com/Illumina/strelka☆37Feb 24, 2017Updated 9 years ago
- The gkno launcher for executing tools or pipelines☆31Jan 17, 2017Updated 9 years ago
- Python interface for Radio Thermostat thermostats☆17Jan 25, 2016Updated 10 years ago
- Ion Torrent SDK Docs☆10Dec 26, 2022Updated 3 years ago
- Utilities to create and analyze gVCF files☆38Mar 21, 2017Updated 9 years ago
- SNAPR: a bioinformatics pipeline for efficient and accurate RNA-seq alignment and analysis☆25Apr 7, 2015Updated 10 years ago
- RNA mapping pipeline☆18Jun 3, 2018Updated 7 years ago
- Demonstrating the PRoot program☆11Jul 29, 2016Updated 9 years ago
- A WGS de novo assembler based on the FMD-index for large genomes☆74Dec 6, 2013Updated 12 years ago
- Aligner for sequencing data☆21Apr 12, 2016Updated 9 years ago
- Fork of https://code.google.com/p/ngs-analysis☆18Sep 14, 2013Updated 12 years ago
- Automated human exome/genome variants detection from FASTQ files☆23Sep 27, 2021Updated 4 years ago
- HPG Aligner is an ultrafast and highly sensitive Next-Generation Sequencing (NGS) mapper which supoprts both DNA and RNA alignment☆34Jul 7, 2017Updated 8 years ago
- Website☆16Aug 30, 2025Updated 6 months ago
- NGS Language Bindings☆120Dec 6, 2023Updated 2 years ago
- an easy deindex tool for illumina multiple barcodes sequencing☆12Jul 30, 2015Updated 10 years ago
- New url: https://github.com/biointec/halvade☆19Apr 19, 2017Updated 8 years ago
- Toolkit to analyze genomic variation data, built on the GATK with Clojure☆66Nov 2, 2015Updated 10 years ago
- The Dinucleotide Quantification Python Package☆11Mar 12, 2022Updated 4 years ago
- Lock-free (Non-blocking) Data Structures in Java☆13Dec 30, 2015Updated 10 years ago
- Go Version of Redis on PMEM☆12Dec 20, 2021Updated 4 years ago
- ☆11Aug 5, 2020Updated 5 years ago
- ☆15Mar 24, 2023Updated 2 years ago
- C++ API & command-line toolkit for working with BAM data☆429May 18, 2025Updated 10 months ago
- This is an old archived repository that we keep for our records. Please use recent GENESIS repository and do not use this one.☆11Sep 15, 2022Updated 3 years ago
- Fast but inaccurate adapter trimmer for Illumina reads☆16Mar 17, 2022Updated 4 years ago
- smith-waterman-gotoh alignment algorithm☆17Sep 1, 2017Updated 8 years ago
- Browser for ExAC consortium data☆106Jan 21, 2022Updated 4 years ago
- Chanjo provides a better way to analyze coverage data in clinical sequencing.☆50Feb 9, 2026Updated last month
- iCodon customizes gene expression based on the codon composition☆15Oct 28, 2023Updated 2 years ago
- A lab management system based on Flask.☆14Aug 19, 2016Updated 9 years ago
- Convert VCF (Variant Call Format) into TCGA MAF (Mutation Annotation Format)☆15Jul 15, 2016Updated 9 years ago
- variant integration methods for the 1000 Genomes Project☆21Jan 16, 2018Updated 8 years ago
- python script to programmatically enrich your data using Enrichr API☆12Jul 5, 2017Updated 8 years ago
- Falcon Accelerated Genomics Pipelines☆15Oct 1, 2019Updated 6 years ago
- Code to run OncoSig Analyses☆18Sep 30, 2020Updated 5 years ago
- The Librarian suite for The Machine from Hewlett Packard Enterprise is the distributed file system that provides access to Fabric-Attache…☆18Jun 7, 2019Updated 6 years ago
- A streamlit app that uses fbprophet for forecasting COVID☆10Dec 8, 2022Updated 3 years ago
- samblaster: a tool to mark duplicates and extract discordant and split reads from sam files.☆238Aug 11, 2021Updated 4 years ago