nickloman / massive-nanopore-sillinessLinks
Very very long reads, indeed
☆13Updated 8 years ago
Alternatives and similar repositories for massive-nanopore-silliness
Users that are interested in massive-nanopore-silliness are comparing it to the libraries listed below
Sorting:
- Homebrew formulae for bioinformatics software only available for Linux☆27Updated 6 years ago
- reference free variant assembly☆34Updated 2 years ago
- blast, shmlast☆21Updated 5 years ago
- Qtip: a tandem simulation approach for accurately predicting read alignment mapping qualities☆25Updated 6 years ago
- Accurate, Lightweight Clustering of de novo Transcriptomes using Fragment Equivalence Classes☆31Updated last year
- What's The Function of these genes?☆22Updated 8 years ago
- Nanopore desc☆18Updated 9 years ago
- Visualise interstrain recombination from environmental samples.☆26Updated 6 years ago
- A program for fast and accurate genome-guided transcripts reconstruction and quantification from RNA-seq (Supporting Pacbio single-end)☆24Updated 4 years ago
- Accurate and fast taxonomic classification using pseudoaligning☆21Updated 8 years ago
- Indel-aware consensus for aligned BAM☆21Updated 2 months ago
- Mapping-free variant caller for short-read Illumina data☆20Updated 5 years ago
- ☆18Updated 9 years ago
- Stupid Simple Structural Variant View☆25Updated 8 years ago
- Genomic Assemblies Merger for NGS☆26Updated last year
- ☆18Updated 8 years ago
- Classify sequencing reads using MinHash.☆48Updated 5 years ago
- Improved multi-sample transcript abundance estimates using adaptive priors☆20Updated 7 years ago
- An ultra fast and accurate paired-end adapter trimmer that needs no a priori adapter sequences.☆22Updated 4 years ago
- ☆13Updated 8 years ago
- SAMsift: advanced filtering and tagging of SAM/BAM alignments using Python expressions.☆23Updated last month
- Mostly deprecated in favor of : https://github.com/hbc/bcbioRNASeq. Quality control, differential gene/transcript expression and pathway …☆24Updated 7 years ago
- R Interface to the NCBI SRA metadata☆23Updated 6 years ago
- ☆18Updated 7 years ago
- ☆36Updated 5 years ago
- SMBL - SnakeMake Bioinformatics Library. Automatic installation of bioinformatics software in your SnakeMake pipelines.☆23Updated 8 years ago
- Online material and code base for the article Coordinates and Intervals in Graph Based Reference Genomes☆11Updated 8 years ago
- The Genome U-Plot is a JavaScript tool to visualize chromosomal abnormalities in the Human Genome using a U-shape layout.☆32Updated 2 years ago
- A utility for splitting mixed origin NGS reads☆10Updated 4 years ago
- Analysis pipeline for functional metagenomic sequencing data obtained using nanopore sequencing☆12Updated 8 years ago