marbl / HG002
A complete diploid human genome
☆96Updated last month
Related projects ⓘ
Alternatives and complementary repositories for HG002
- Tandem repeat genotyping and visualization from PacBio HiFi data☆105Updated last month
- Stratification BED files from the Global Alliance for Genomics and Health (GA4GH) Benchmarking Team and the Genome in a Bottle Consortium…☆75Updated last year
- A tool to identify, orient, trim and rescue full length cDNA reads☆80Updated 2 years ago
- accurate LiftOver tool for new genome assemblies☆110Updated 3 months ago
- Research release basecalling models and configurations☆103Updated 4 months ago
- Wally: Visualization of aligned sequencing reads and contigs☆108Updated last month
- Pangenome-based genome inference☆111Updated this week
- ClairS - a deep-learning method for long-read somatic small variant calling☆73Updated 3 weeks ago
- A *fast* tool for BAM/CRAM quality evaluation, intended for long reads☆127Updated this week
- Evaluation and polishing workflows for T2T genome assemblies☆104Updated 3 weeks ago
- pbsv - PacBio structural variant (SV) calling and analysis tools☆129Updated last week
- A tool for somatic structural variant calling using long reads☆102Updated this week
- Constructing a pangenome gene graph☆174Updated 3 months ago
- vcfdist: Accurately benchmarking phased variant calls☆76Updated last week
- Variant calling tool for long-read sequencing data☆100Updated 5 months ago
- ☆97Updated last year
- Fast and accurate coordinate conversion between assemblies☆108Updated last month
- Jasmine: SV Merging Across Samples☆180Updated last year
- ☆150Updated last month
- Collection of tools for the analysis of CpG data☆72Updated 8 months ago
- ☆103Updated this week
- Pairwise whole genome aligner☆136Updated this week
- abPOA: an SIMD-based C library for fast partial order alignment using adaptive band☆118Updated last week
- A bioinformatics tool for working with modified bases☆140Updated last month
- GraffiTE is a pipeline that finds polymorphic transposable elements in genome assemblies and/or long reads, and genotypes the discovered …☆112Updated this week
- Visualise and analyse nanopore (ONT) raw signals☆108Updated 2 months ago
- Structural Variant Identification Method using Long Reads☆155Updated 3 years ago
- Same species annotation lift over pipeline.☆96Updated last year
- Comprehensive TE insertion identification with WGS/WES data from multiple sequencing technics☆102Updated 4 months ago
- Dfam Transposable Element Tools Docker container.☆84Updated last month