☆14Nov 11, 2026Updated this week
Alternatives and similar repositories for Himito
Users that are interested in Himito are comparing it to the libraries listed below. We may earn a commission when you buy through links labeled 'Ad' on this page.
Sorting:
- ☆10Jul 2, 2026Updated 4 months ago
- pblab: PacBio HiFi analysis tools☆22Oct 21, 2026Updated 3 weeks ago
- Kmer Analysis of Pileups for Genotyping☆44Jul 16, 2026Updated 3 months ago
- Copy number variant caller and depth visualization utility for PacBio HiFi reads☆51Oct 22, 2024Updated 2 years ago
- Using DNA methylation to resolve cell-specific variant assignments in bulk only long-read sequencing data☆11Oct 7, 2026Updated last month
- Managed hosting for WordPress and PHP on Cloudways • AdManaged hosting for WordPress, Magento, Laravel, or PHP apps, on multiple cloud providers. Deploy in minutes on Cloudways by DigitalOcean.
- KaryoScope: rapid, alignment-free sequence annotation for the pangenome era☆29Nov 5, 2026Updated last week
- Parakit is a tool to analyze the RCCX module, which contain the CYP21A2 gene, using long sequencing reads.☆19Oct 26, 2026Updated 2 weeks ago
- ☆15Sep 15, 2025Updated last year
- rust tool to choose the best read alignment between haploids to a diploid reference genome☆31Oct 20, 2026Updated 3 weeks ago
- online variation graph induction☆12Oct 21, 2025Updated last year
- A method to locate variation clusters☆11Nov 27, 2025Updated 11 months ago
- Fast SAM/BAM sorter.☆12Nov 3, 2026Updated last week
- A tool for sniffing out the differences in vari-Ants☆60Oct 30, 2026Updated last week
- A battery of methylation tools for PacBio HiFi reads☆58Nov 2, 2026Updated last week
- Wordpress hosting with auto-scaling - Free Trial Offer • AdFully Managed hosting for WordPress and WooCommerce businesses that need reliable, auto-scalable performance. Cloudways SafeUpdates now available.
- pangenome alignment, implicit/explicit graph, and variants for human pangenome project release 2☆24Sep 9, 2026Updated 2 months ago
- Small variant, structural variant, and short tandem repeat phasing tool for PacBio HiFi reads☆88Oct 28, 2026Updated 2 weeks ago
- VolcanoSV enables accurate and robust structural variant calling in diploid genomes from single-molecule long read sequencing☆10Sep 8, 2026Updated 2 months ago
- This tools counts the number of specific k-mers within sequence data. The counts can then be compare to other counts to determine to comp…☆32Nov 25, 2024Updated last year
- Plot multiple sequence alignment (MSA)☆17Apr 21, 2026Updated 6 months ago
- Blazingly fast, streaming duplicate detection for NGS data☆22Updated this week
- A wrapper for calling small variants from human germline high-coverage single-sample Illumina data☆14Jul 21, 2019Updated 7 years ago
- Mosaic Genome Assembler☆29Sep 14, 2026Updated last month
- ☆44Jan 14, 2026Updated 9 months ago
- GPUs on demand by Runpod - Special Offer Available • AdRun AI, ML, and HPC workloads on powerful cloud GPUs—without limits or wasted spend. Deploy GPUs in under a minute and pay by the second.
- Nanopore sequencing-based episignature detection☆19Jun 10, 2026Updated 5 months ago
- LongcallD: joint calling and phasing of small, structural and mosaic variants from long reads☆113Jun 25, 2026Updated 4 months ago
- Genotyping of copy number sensitive allele-specific haplotypes☆29Aug 28, 2026Updated 2 months ago
- ☆22May 8, 2026Updated 6 months ago
- Functions to compare a SV call sets against a truth set.☆32Jun 18, 2025Updated last year
- Python package for comparing genome assemblies and read data to the diploid Q100 benchmark☆22Oct 8, 2026Updated last month
- ☆14May 2, 2025Updated last year
- ☆135Nov 1, 2026Updated last week
- Error correction of long reads☆16Jan 30, 2026Updated 9 months ago
- Wordpress hosting with auto-scaling - Free Trial Offer • AdFully Managed hosting for WordPress and WooCommerce businesses that need reliable, auto-scalable performance. Cloudways SafeUpdates now available.
- Svirlpool: structural variant detection from long read sequencing by local assembly☆10Oct 11, 2026Updated last month
- Application of pan-genome for population☆122Oct 26, 2025Updated last year
- A segmentation approach to analyze DNA methylation patterns and identify differentially methylation regions from whole-genome datasets☆22Sep 3, 2026Updated 2 months ago
- bioinformatics toolkit in rust☆118Aug 16, 2026Updated 2 months ago
- ☆33Jun 18, 2026Updated 4 months ago
- Spiritual successor to picard for sequencing qc☆65Updated this week
- Optimal sequence-to-graph alignment with recombinations☆41Apr 28, 2026Updated 6 months ago
Are these results useful?