wjidea / defusion
defusion
☆14Updated 3 years ago
Alternatives and similar repositories for defusion:
Users that are interested in defusion are comparing it to the libraries listed below
- Nucmer from Mummer3 followed by ggplot for nicer and more customisable genome alignment plots.☆11Updated 4 years ago
- An R package for comparative transcriptomic analyses of hybrids and their progenitors☆14Updated 7 months ago
- A loose collection of scripts and utilities for processing and analyzing the Goat reference genome assembly☆11Updated 8 years ago
- parallelLastz: Running Lastz in parallel☆16Updated 7 months ago
- PanEffect is a JavaScript framework to explore variant effects across a pangenome. The tool has two views that allows a user to (1) expl…☆13Updated last year
- A program to generate a graph which presents a simplified representation of several full length genomes☆12Updated 6 years ago
- Simple tools for working with Hi-C data☆17Updated 6 years ago
- Identification of conserved non-coding sequences in plants☆17Updated 3 months ago
- Gene copy number prediction from k-mer frequencies☆13Updated 8 months ago
- ☆12Updated 7 years ago
- HAT is a set of tools for calling de novo variants from whole-genome sequencing data.☆23Updated last year
- SINE annotation tool for plant genomes☆17Updated last year
- Pipeline for genome scaffolding by modelling distributions of HiC pairs☆9Updated 2 years ago
- Scripts to do haplotype analysis on pan genomes.☆21Updated 4 years ago
- Consensus genome annotation using OMA☆23Updated 4 months ago
- ☆15Updated 4 years ago
- Simultaneous multi-sample transcript assembler for RNA-seq data☆17Updated 4 months ago
- Set of script for the paper on the cattle graph genome☆13Updated 2 years ago
- ☆12Updated 10 months ago
- Kmer based genotyper for short reads.☆23Updated 3 years ago
- A comparative genome scaffolding tool☆17Updated 6 years ago
- Tandem Repeats Finder: a program to analyze DNA sequences☆14Updated 2 years ago
- De-novo Assembly Structural Variant Caller☆13Updated 8 years ago
- ☆14Updated last year
- Genome Assembly 102☆14Updated this week
- A reliable gap filling pipeline for draft genomes☆11Updated 5 years ago
- Prefix-renaming FASTA records really fast.☆17Updated 10 months ago
- A framework for extracting telomeric reads from single-molecule sequencing experiments, describing their sequence variation and motifs, a…☆16Updated last year
- Infering ancestral synteny with hierarchical orthologous groups☆14Updated this week
- ☆12Updated 4 years ago