marbl / HG002Links
A complete diploid human genome
☆134Updated 2 weeks ago
Alternatives and similar repositories for HG002
Users that are interested in HG002 are comparing it to the libraries listed below
Sorting:
- Tandem repeat genotyping and visualization from PacBio HiFi data☆125Updated 2 months ago
- A tool for somatic structural variant calling using long reads☆146Updated last week
- Wally: Visualization of aligned sequencing reads and contigs☆118Updated 5 months ago
- Fast and accurate coordinate conversion between assemblies☆116Updated 2 weeks ago
- Phased assembly variant caller☆126Updated 10 months ago
- Pangenome-based genome inference☆147Updated 2 months ago
- pbsv - PacBio structural variant (SV) calling and analysis tools☆159Updated 7 months ago
- Stratification BED files from the Global Alliance for Genomics and Health (GA4GH) Benchmarking Team and the Genome in a Bottle Consortium…☆82Updated 2 years ago
- Yet another k-mer analyzer☆143Updated last year
- Jasmine: SV Merging Across Samples☆227Updated 9 months ago
- accurate LiftOver tool for new genome assemblies☆135Updated last year
- Visualise and analyse nanopore (ONT) raw signals☆122Updated last month
- A tool to identify, orient, trim and rescue full length cDNA reads☆82Updated 3 years ago
- Collection of tools for the analysis of CpG data☆95Updated 3 months ago
- ☆117Updated last month
- PBSIM3: a simulator for all types of PacBio and ONT long reads☆83Updated 5 months ago
- Tools for plotting methylation data in various ways☆160Updated last week
- Detecting genome structural variants with deep learning in single molecule sequencing☆113Updated 6 months ago
- A list of software for pangenomics☆131Updated 2 weeks ago
- Dfam Transposable Element Tools Docker container.☆100Updated 3 weeks ago
- Research release basecalling models and configurations☆114Updated 4 months ago
- Tandem repeat expansion detection or genotyping from long-read alignments☆127Updated last month
- Same species annotation lift over pipeline.☆98Updated 2 years ago
- GenMap - Fast and Exact Computation of Genome Mappability☆113Updated last year
- ☆119Updated last year
- A *fast* tool for BAM/CRAM quality evaluation, intended for long reads☆162Updated last week
- Structural Variant Identification Method using Long Reads☆175Updated 4 years ago
- RNA modifications detection from Nanopore dRNA-Seq data☆87Updated last month
- Toolkit for calling structural variants using short or long reads☆109Updated 2 weeks ago
- GraffiTE is a pipeline that finds polymorphic transposable elements in genome assemblies and/or long reads, and genotypes the discovered …☆200Updated last week