marbl / HG002Links
A complete diploid human genome
☆140Updated 3 months ago
Alternatives and similar repositories for HG002
Users that are interested in HG002 are comparing it to the libraries listed below
Sorting:
- A tool for somatic structural variant calling using long reads☆160Updated 3 months ago
- Tandem repeat genotyping and visualization from PacBio HiFi data☆131Updated last month
- Wally: Visualization of aligned sequencing reads and contigs☆120Updated 3 months ago
- Fast and accurate coordinate conversion between assemblies☆118Updated 3 months ago
- Visualise and analyse nanopore (ONT) raw signals☆126Updated last month
- Stratification BED files from the Global Alliance for Genomics and Health (GA4GH) Benchmarking Team and the Genome in a Bottle Consortium…☆83Updated 3 years ago
- Pangenome-based genome inference☆153Updated last month
- Yet another k-mer analyzer☆158Updated 3 weeks ago
- accurate LiftOver tool for new genome assemblies☆147Updated last year
- pbsv - PacBio structural variant (SV) calling and analysis tools☆160Updated 10 months ago
- GenMap - Fast and Exact Computation of Genome Mappability☆113Updated last year
- Phased assembly variant caller☆132Updated last year
- Collection of tools for the analysis of CpG data☆103Updated 6 months ago
- Research release basecalling models and configurations☆117Updated 8 months ago
- Detecting genome structural variants with deep learning in single molecule sequencing☆116Updated 9 months ago
- ☆126Updated 2 years ago
- ☆121Updated this week
- A *fast* tool for BAM/CRAM quality evaluation, intended for long reads☆164Updated last week
- Constructing a pangenome gene graph☆203Updated 5 months ago
- A list of software for pangenomics☆165Updated last week
- Structural Variant Identification Method using Long Reads☆181Updated 4 years ago
- Tools for plotting methylation data in various ways☆166Updated last month
- Jasmine: SV Merging Across Samples☆237Updated last year
- Toolkit for calling structural variants using short or long reads☆115Updated last week
- ClairS - a deep-learning method for long-read somatic small variant calling☆102Updated last month
- PBSIM3: a simulator for all types of PacBio and ONT long reads☆98Updated 9 months ago
- Somatic structural variant caller for long-read data☆87Updated 2 months ago
- A tool to identify, orient, trim and rescue full length cDNA reads☆83Updated 3 years ago
- Dfam Transposable Element Tools Docker container.☆101Updated last month
- Variant calling tool for long-read sequencing data☆116Updated 10 months ago