broadinstitute / pilon
Pilon is an automated genome assembly improvement and variant detection tool
☆345Updated 2 years ago
Alternatives and similar repositories for pilon:
Users that are interested in pilon are comparing it to the libraries listed below
- A tool for generating consensus long-read assemblies for bacterial genomes☆314Updated 8 months ago
- pycoQC computes metrics and generates Interactive QC plots from the sequencing summary report generated by Oxford Nanopore technologies b…☆273Updated 3 months ago
- (Not Offical) BBMap short read aligner, and other bioinformatic tools.☆215Updated 3 years ago
- quality filtering tool for long reads☆310Updated last year
- An overview of all nanopack tools☆230Updated last year
- Eukaryotic Genome Annotation Pipeline☆330Updated last week
- Ultrafast consensus module for raw de novo genome assembly of long uncorrected reads. http://genome.cshlp.org/content/early/2017/01/18/gr…☆276Updated 8 months ago
- Filtering and trimming of long read sequencing data☆197Updated 2 years ago
- RepeatMasker is a program that screens DNA sequences for interspersed repeats and low complexity DNA sequences.☆240Updated 2 months ago
- Bracken (Bayesian Reestimation of Abundance with KrakEN) is a highly accurate statistical method that computes the abundance of species i…☆299Updated 6 months ago
- Tools for fast and flexible genome assembly scaffolding and improvement☆486Updated 11 months ago
- KrakenTools provides individual scripts to analyze Kraken/Kraken2/Bracken/KrakenUniq output files☆326Updated last year
- BRAKER is a pipeline for fully automated prediction of protein coding gene structures with GeneMark-ES/ET/EP/ETP and AUGUSTUS in novel eu…☆374Updated last week
- PacBio Secondary Analysis Tools on Bioconda. Contains list of PacBio packages available via conda.☆259Updated 7 months ago
- A tool to circularize genome assemblies☆235Updated 9 months ago
- MCScanX: Multiple Collinearity Scan toolkit X version. The most popular synteny analysis tool in the world!☆247Updated last month
- NGMLR is a long-read mapper designed to align PacBio or Oxford Nanopore (standard and ultra-long) to a reference genome with a focus on r…☆295Updated 10 months ago
- adapter trimmer for Oxford Nanopore reads☆348Updated 8 months ago
- Tool to plot synteny and structural rearrangements between genomes☆294Updated 2 months ago
- Telomere-to-telomere assembly of accurate long reads (PacBio HiFi, Oxford Nanopore Duplex, HERRO corrected Oxford Nanopore Simplex) and O…☆315Updated this week
- Genome Assembly and Annotation Service code☆206Updated last year
- TransDecoder source☆283Updated 3 months ago
- Sequence correction provided by ONT Research☆435Updated 3 months ago
- Fast and accurately polish the genome generated by long reads.☆217Updated 3 weeks ago
- Fast and accurate de novo assembler for long reads☆376Updated 8 months ago
- Synteny and Rearrangement Identifier☆357Updated last month
- Bacterial ribosomal RNA predictor☆232Updated last year
- Scan contig files against PubMLST typing schemes☆210Updated 2 years ago
- Iso-Seq - Scalable De Novo Isoform Discovery from Single-Molecule PacBio Reads☆200Updated 3 months ago
- 3D de novo assembly (3D DNA) pipeline☆207Updated last year