DNA序列比对结果 可视化展示工具
☆47Oct 10, 2021Updated 5 years ago
Alternatives and similar repositories for LINKVIEW
Users that are interested in LINKVIEW are comparing it to the libraries listed below. We may earn a commission when you buy through links labeled 'Ad' on this page.
Sorting:
- DNA序列比对结果 可视化展示工具☆58Dec 18, 2022Updated 3 years ago
- ☆45May 8, 2024Updated 2 years ago
- ☆16Apr 9, 2021Updated 5 years ago
- ☆14May 22, 2025Updated last year
- Structural Variant Identification Method using Genome Assemblies☆148Sep 16, 2022Updated 4 years ago
- Deploy open-source AI quickly and easily - Special Bonus Offer • AdRunpod Hub is built for open source. One-click deployment and autoscaling endpoints without provisioning your own infrastructure.
- HiC-Hiker: A probabilistic model to determine contig orientation in chromosome-length scaffolds with Hi-C☆26Jan 14, 2021Updated 5 years ago
- Extracting paths from assembly graphs☆26Jun 22, 2026Updated 4 months ago
- ☆78Jun 12, 2020Updated 6 years ago
- A Plant Presence/absence Variants Scanner and Pan-genome Construction Pipeline☆27May 24, 2021Updated 5 years ago
- ☆83Jun 2, 2023Updated 3 years ago
- ☆12Jun 7, 2024Updated 2 years ago
- Create a pseudohaploid assembly from a partially resolved diploid assembly☆32Nov 22, 2019Updated 6 years ago
- ☆11Jan 13, 2021Updated 5 years ago
- Generate an interactive dot plot from mummer or minimap alignments☆219Jan 17, 2024Updated 2 years ago
- 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.
- ☆89Oct 12, 2026Updated 2 weeks ago
- bash script to search for centromeric repeat patterns in PacBio data, using several current tools (trf and R)☆13Dec 1, 2016Updated 9 years ago
- ☆16Jan 10, 2022Updated 4 years ago
- Reference-based variant calling pipeline for a pair of phased haplotype assemblies☆120Jun 6, 2021Updated 5 years ago
- A mass non-curated database of potential telomeric repeat sequences across the eukaryotic tree of life.☆13Oct 10, 2026Updated 2 weeks ago
- WGDI: A user-friendly toolkit for evolutionary analyses of whole-genome duplications and ancestral karyotypes☆176Nov 4, 2025Updated 11 months ago
- B73Ab10 genome assembly methods☆17Jan 21, 2022Updated 4 years ago
- PECAT, a phased error correct and assembly tool☆69Dec 8, 2025Updated 10 months ago
- Code to compute the XP-CLR statistic to infer natural selection☆108Jun 13, 2022Updated 4 years ago
- Simple, predictable pricing with DigitalOcean hosting • AdAlways know what you'll pay with monthly caps and flat pricing. Enterprise-grade infrastructure trusted by 600k+ customers.
- ☆51Jul 23, 2025Updated last year
- A gap-closing software tool that uses long reads to enhance genome assembly.☆251Sep 6, 2024Updated 2 years ago
- Long-reads Gap-free Chromosome-scale Assembler☆79Mar 21, 2023Updated 3 years ago
- Bash scripts and data used in pantranscriptomic paper☆25Oct 21, 2022Updated 4 years ago
- Repository for Colantonio et al., 2022, "Metabolomic Selection for Enhanced Fruit Flavor"☆12Feb 7, 2022Updated 4 years ago
- Draw a dot plot from a paf alignment☆47May 9, 2026Updated 5 months ago
- Close assembly gaps using long-reads at high accuracy.☆52Feb 20, 2024Updated 2 years ago
- ☆37Aug 3, 2026Updated 2 months ago
- A program to call variants from genome alignment☆84Apr 29, 2025Updated last year
- Deploy on Railway without the complexity - Free Credits Offer • AdConnect your repo and Railway handles the rest with instant previews. Quickly provision container image services, databases, and storage volumes.
- ☆30Jul 16, 2022Updated 4 years ago
- RegCloser is a genome gap-closing tool based on the robust regression approach, which is conceptually applicable to de novo assembly of N…☆16Apr 22, 2024Updated 2 years ago
- Nanopore data assembler☆171Mar 27, 2022Updated 4 years ago
- TGSFilter: An ultra-fast and efficient tool for long reads filtering and trimming☆28May 18, 2024Updated 2 years ago
- Synteny and Rearrangement Identifier☆496Jul 1, 2026Updated 3 months ago
- Sensitive alignment of genomes with high sequence diversity, extensive structural polymorphism and whole-genome duplication variation☆203Aug 17, 2026Updated 2 months ago
- ☆42May 19, 2025Updated last year