indexofire / ndafp
New version
☆33Updated 8 years ago
Alternatives and similar repositories for ndafp:
Users that are interested in ndafp are comparing it to the libraries listed below
- Helper scripts for biological data processing from Sentieon☆63Updated 3 months ago
- Snakemake pipelines for nanopore sequencing data archiving and processing☆88Updated 3 years ago
- A simple plot library☆52Updated 7 years ago
- Scripts for next generation sequencing☆48Updated 5 years ago
- Lima - Demultiplex Barcoded PacBio Samples☆65Updated 3 months ago
- This repository houses the code to run SURPI+, a rapid computational pipeline for comprehensive identification of pathogens from clinical…☆40Updated 5 years ago
- Workflow for Building Microsynteny Networks☆50Updated 2 years ago
- Tools for working with second gen assemblies, fasta sequences, etc☆92Updated 8 years ago
- PacBio Assembly Tool Suite: Reads in ⇨ Assembly out☆115Updated 4 years ago
- Pair-End AssembeR☆30Updated 10 years ago
- ☆88Updated 4 years ago
- ☆70Updated 4 years ago
- Simple code snippets and data for the One Flowcell - One Assembly study☆36Updated 7 years ago
- This script will extract the intron feature gff3 and sequence from gene_exon gff3 and fasta file.☆33Updated 6 years ago
- Genome Scripts used in fungal comparative genomics☆65Updated 4 years ago
- ☆32Updated 2 years ago
- Genomic related tools☆71Updated 3 years ago
- Automates running of OrthoMCL software from http://orthomcl.org/common/downloads/software/v2.0/☆80Updated 4 years ago
- My collection of light bioinformatics analysis pipelines for specific tasks☆72Updated 9 months ago
- Accurate and rapid RiboRNA sequences Detector based on deep learning☆105Updated last year
- LRSDAY: Long-read Sequencing Data Analysis for Yeasts☆32Updated 11 months ago
- convert various features into a GFF-like file for use in genome browsers☆69Updated last year
- Software for clustering de novo assembled transcripts and counting overlapping reads☆70Updated 3 years ago
- ☆51Updated 6 years ago
- A method for circular DNA detection based on probabilistic mapping of ultrashort reads☆61Updated 7 months ago
- qcat is a Python command-line tool for demultiplexing Oxford Nanopore reads from FASTQ files.☆78Updated 4 years ago
- 10x Genomics Linked-Read Diploid De Novo Assembler☆65Updated 6 years ago
- A general metagenomics data mining system focus on robust microbiome research☆56Updated 5 months ago
- FEELnc : FlExible Extraction of LncRNA☆85Updated 5 months ago
- PCR Primer Quality Control☆59Updated 11 months ago