marbl / HG002Links
A complete diploid human genome
☆120Updated 4 months ago
Alternatives and similar repositories for HG002
Users that are interested in HG002 are comparing it to the libraries listed below
Sorting:
- Wally: Visualization of aligned sequencing reads and contigs☆117Updated last month
- ☆112Updated 3 weeks ago
- Fast and accurate coordinate conversion between assemblies☆113Updated 2 months ago
- Pangenome-based genome inference☆127Updated last month
- A tool for somatic structural variant calling using long reads☆134Updated last month
- Research release basecalling models and configurations☆110Updated 2 weeks ago
- Phased assembly variant caller☆116Updated 6 months ago
- A tool to identify, orient, trim and rescue full length cDNA reads☆82Updated 2 years ago
- pbsv - PacBio structural variant (SV) calling and analysis tools☆149Updated 3 months ago
- Visualise and analyse nanopore (ONT) raw signals☆116Updated 4 months ago
- ClairS - a deep-learning method for long-read somatic small variant calling☆84Updated last month
- A *fast* tool for BAM/CRAM quality evaluation, intended for long reads☆151Updated 2 months ago
- Toolkit for calling structural variants using short or long reads☆104Updated 2 weeks ago
- Jasmine: SV Merging Across Samples☆215Updated 5 months ago
- accurate LiftOver tool for new genome assemblies☆126Updated 9 months ago
- Tandem repeat genotyping and visualization from PacBio HiFi data☆117Updated last month
- Collection of tools for the analysis of CpG data☆82Updated 4 months ago
- Simple pileup-based variant caller☆90Updated last month
- A list of software for pangenomics☆114Updated 3 weeks ago
- ☆114Updated last year
- Tandem repeat expansion detection or genotyping from long-read alignments☆114Updated this week
- Stratification BED files from the Global Alliance for Genomics and Health (GA4GH) Benchmarking Team and the Genome in a Bottle Consortium…☆79Updated 2 years ago
- Dfam Transposable Element Tools Docker container.☆91Updated 3 weeks ago
- ☆48Updated 9 months ago
- vcfdist: Accurately benchmarking phased variant calls☆80Updated last month
- ☆94Updated 2 weeks ago
- PBSIM3: a simulator for all types of PacBio and ONT long reads☆76Updated last month
- Variant calling tool for long-read sequencing data☆110Updated 2 months ago
- Pipeline for calling structural variations in whole genomes sequencing Oxford Nanopore data☆114Updated 3 years ago
- Long read aligner☆115Updated 2 years ago