songbowang125 / SVision-proLinks
☆48Updated 4 months ago
Alternatives and similar repositories for SVision-pro
Users that are interested in SVision-pro are comparing it to the libraries listed below
Sorting:
- Copy number variant caller and depth visualization utility for PacBio HiFi reads☆47Updated last year
- Application of pan-genome for population☆116Updated 2 months ago
- ☆78Updated 5 years ago
- Public Benchmark of Long-Read Structural Variant Caller on PacBio CCS HG002 Data☆51Updated 4 years ago
- A pipeline to de novo assemble the stLFR reads using Supernova Assembler☆20Updated 2 years ago
- C-Phasing/CPhasing: Phasing and scaffolding polyploid genomes based on Pore-C, HiFi-C/CiFi or Hi-C.☆82Updated last week
- Variant annotation and merging pipeline☆41Updated 5 months ago
- A collection of scripts for working with Hi-C data, Juicebox, and other genomic file formats☆69Updated 4 years ago
- A novel genome assembly pipeline based on deep learning☆67Updated last year
- Structural variant caller for real-time long-read sequencing data☆61Updated 3 years ago
- Error correction of ONT transcript reads☆58Updated 2 years ago
- Genome scaffolding based on HiC data in heterozygous and high ploidy genomes☆60Updated last year
- SRF: Satellite Repeat Finder☆101Updated 2 years ago
- Tools for improving the sensitivity and specificity of genome alignments☆58Updated 2 years ago
- Set of tools to manipulate and visualize modified base bam files☆58Updated 3 years ago
- Collection of tools for the analysis of CpG data☆103Updated 6 months ago
- Methylation Phasing for Nanopore Sequencing☆49Updated 2 years ago
- Copy number caller for long read data including SNV utilization☆68Updated 9 months ago
- ☆83Updated 10 months ago
- ☆22Updated 4 years ago
- Code for phasing SVs with SNPs☆52Updated 5 years ago
- tomato graph pangenome☆86Updated 3 years ago
- PhyloAcc a software to detect the changes of conservation of a genomic region☆34Updated 2 months ago
- DNA序列比对结果 可视化展示工具☆57Updated 3 years ago
- A pipeline for isoseq☆23Updated 7 years ago
- ☆45Updated 9 years ago
- Reference-based variant calling pipeline for a pair of phased haplotype assemblies☆105Updated 4 years ago
- Structural Variants Pipeline for Long Reads☆44Updated 7 years ago
- Detecting genome structural variants with deep learning in single molecule sequencing☆116Updated 9 months ago
- Joint structural variant and copy number variant caller for HiFi sequencing data☆69Updated 2 months ago