najoshi / sabreLinks
☆64Updated 5 years ago
Alternatives and similar repositories for sabre
Users that are interested in sabre are comparing it to the libraries listed below
Sorting:
- Building SuperTranscripts: A linear representation of transcriptome data☆68Updated 4 years ago
- Maximum likelihood demultiplexing☆50Updated 11 months ago
- PrimerTree: Visually Assessing the Specificity and Informativeness of Primer Pairs☆52Updated 3 months ago
- ☆78Updated 11 years ago
- Software for clustering de novo assembled transcripts and counting overlapping reads☆76Updated 4 years ago
- A catalogue of available long read sequencing data analysis tools☆85Updated last month
- BigWig and BAM utilities☆102Updated last year
- Evolutionary Transcriptomics with R☆47Updated this week
- ☆96Updated 3 years ago
- A read extraction and realignment tool for next generation sequencing data☆104Updated 3 years ago
- Nanopore data analysis in R☆40Updated 2 years ago
- Quickly calculate and visualize sequence coverage in alignment files☆100Updated 6 years ago
- GFF3sort: A Perl Script to sort gff3 files and produce suitable results for tabix tools☆50Updated 5 years ago
- Software for predicting library complexity and genome coverage in high-throughput sequencing.☆94Updated last month
- Tip and tricks for BAM files☆86Updated 7 years ago
- 10x Genomics Linked-Read Diploid De Novo Assembler☆65Updated 7 years ago
- Toolkit for processing TAB-delimited format☆62Updated last year
- R package for inferring copy number from read depth☆32Updated 3 years ago
- An awk-like VCF parser☆56Updated 2 years ago
- web documentation for Trinotate☆48Updated 3 years ago
- A simple toolset for BED files (warning: CLI may change before bedtk becomes stable)☆143Updated 5 months ago
- Tools and software library developed by the ONT Applications group☆64Updated 5 years ago
- NGSNGS: Next generation simulator for next generation sequencing data☆56Updated last year
- Annocript is a pipeline for the annotation of de-novo generated transcriptomes. It executes BLAST analysis with UniProt, NCBI Conserved …☆56Updated 5 years ago
- High-performance error correction for Illumina resequencing data☆74Updated 9 years ago
- A reference viral database (RVDB)☆26Updated 7 years ago
- Miscellaneous Bioinformatics scripts etc mostly in Python☆45Updated last week
- A collection of command line tools for working with sequencing data☆52Updated 2 weeks ago
- For biological deep sequencing data. Decompose a UCSC knownGenes/Ensembl GTF file into transcript regions (i.e. exons, introns, UTRs and…☆36Updated 2 years ago
- An NGS read trimming tool that is specific, sensitive, and speedy. (production)☆126Updated 9 months ago