EichlerLab / pavLinks
Phased assembly variant caller
☆125Updated 9 months ago
Alternatives and similar repositories for pav
Users that are interested in pav are comparing it to the libraries listed below
Sorting:
- Pangenome-based genome inference☆146Updated last month
- Tandem repeat genotyping and visualization from PacBio HiFi data☆124Updated last month
- Collection of tools for the analysis of CpG data☆93Updated 2 months ago
- Reference-based variant calling pipeline for a pair of phased haplotype assemblies☆103Updated 4 years ago
- Wally: Visualization of aligned sequencing reads and contigs☆117Updated 5 months ago
- ☆116Updated 2 weeks ago
- Application of pan-genome for population☆109Updated 11 months ago
- Structural Variant Identification Method using Genome Assemblies☆123Updated 3 years ago
- A list of software for pangenomics☆128Updated 2 weeks ago
- Pipeline to convert a haploid assembly into diploid☆103Updated 7 months ago
- Yet another k-mer analyzer☆143Updated last year
- Mapping pipeline for data generated using Arima-HiC☆80Updated last year
- Evaluating genome assemblies☆105Updated last week
- Panacus is a tool for computing statistics for GFA-formatted pangenome graphs☆110Updated last month
- Make colorful identity heatmaps of genomic sequence☆119Updated last year
- accurate LiftOver tool for new genome assemblies☆134Updated last year
- Toolkit for calling structural variants using short or long reads☆109Updated last week
- Structural Variant Identification Method using Long Reads☆173Updated 4 years ago
- Fast and accurate coordinate conversion between assemblies☆115Updated last week
- PBSIM3: a simulator for all types of PacBio and ONT long reads☆81Updated 4 months ago
- A tool for somatic structural variant calling using long reads☆145Updated last month
- Same species annotation lift over pipeline.☆98Updated 2 years ago
- Copy number caller for long read data including SNV utilization☆67Updated 5 months ago
- Few scripts facilitating the extraction of info from Repeat Masker .out files☆83Updated 4 years ago
- Simple pileup-based variant caller☆91Updated 4 months ago
- Structural variant caller for real-time long-read sequencing data☆57Updated 2 years ago
- ☆138Updated 4 months ago
- Constructing a pangenome gene graph☆194Updated last month
- ☆49Updated last year
- VarIant SimulatOR for short, long and linked reads☆48Updated 10 months ago