ANGSD / angsdLinks
Program for analysing NGS data.
☆237Updated 3 months ago
Alternatives and similar repositories for angsd
Users that are interested in angsd are comparing it to the libraries listed below
Sorting:
- Convert SNPs in VCF format to PHYLIP, NEXUS, binary NEXUS, or FASTA alignments for phylogenetic analysis☆312Updated last year
- NOVOPlasty - The organelle assembler and heteroplasmy caller☆188Updated last year
- Inference of ploidy and heterozygosity structure using whole genome sequencing data☆271Updated 2 weeks ago
- Genome Assembly and Annotation Service code☆213Updated last year
- ⚡♠️ Assemble bacterial isolate genomes from Illumina paired-end reads☆229Updated 2 years ago
- Fast genome analysis from unassembled short reads☆292Updated last year
- Filtering and trimming of long read sequencing data☆206Updated 2 years ago
- SMC++ infers population history from whole-genome sequence data.☆168Updated last year
- Implementation of the Pairwise Sequentially Markovian Coalescent (PSMC) model☆170Updated 2 years ago
- A simple and fast metassembler and assembly gap filler designed for long molecule based assemblies.☆204Updated 2 years ago
- Generate an interactive dot plot from mummer or minimap alignments☆203Updated last year
- VGP repository for the genome assembly working group☆193Updated last month
- Fast calculation of Patterson's D (ABBA-BABA) and the f4-ratio statistics across many populations/species☆174Updated 6 months ago
- RepeatMasker is a program that screens DNA sequences for interspersed repeats and low complexity DNA sequences.☆262Updated last month
- Tool to plot synteny and structural rearrangements between genomes☆308Updated 2 months ago
- Synteny and Rearrangement Identifier☆390Updated last month
- ☆211Updated 5 months ago
- LTR_retriever is a highly accurate and sensitive program for identification of LTR retrotransposons; The LTR Assembly Index (LAI) is also…☆205Updated this week
- A tool for generating consensus long-read assemblies for bacterial genomes☆324Updated last year
- Pilon is an automated genome assembly improvement and variant detection tool☆367Updated 3 years ago
- Fast and accurately polish the genome generated by long reads.☆226Updated 5 months ago
- Find, circularise and annotate mitogenome from PacBio assemblies☆183Updated last month
- PopLDdecay: a fast and effective tool for linkage disequilibrium decay analysis based on variant call format(VCF) files☆192Updated 10 months ago
- pycoQC computes metrics and generates Interactive QC plots from the sequencing summary report generated by Oxford Nanopore technologies b…☆281Updated 8 months ago
- haplotypic duplication identification tool☆247Updated last year
- Software for painlessly estimating average nucleotide diversity within and between populations☆136Updated last month
- quality filtering tool for long reads☆346Updated last year
- General tools for genomic analyses.☆365Updated 4 months ago
- Effective selection of population size projection for construction of the site frequency spectrum. Convert VCF to dadi/fastsimcoal style …☆154Updated 10 months ago
- ALLHiC: phasing and scaffolding polyploid genomes based on Hi-C data☆177Updated 8 months ago