ntpz870817 / ChamaeleoLinks
BGI DNA Storage Kit
☆42Updated 4 months ago
Alternatives and similar repositories for Chamaeleo
Users that are interested in Chamaeleo are comparing it to the libraries listed below
Sorting:
- Program designed for DNA storage using Yin-Yang transcoding algorithm☆28Updated last year
- SPIDER-WEB generates coding algorithms with superior error tolerance and real-time information retrieval capacity☆10Updated 11 months ago
- ☆11Updated this week
- ☆63Updated 5 months ago
- Xron - an omni basecaller for ONT reads.☆22Updated 6 months ago
- BaseNet: A Transformer-Based Toolkit for Nanopore Sequencing Signal Decoding☆12Updated 2 months ago
- DeepMod: a deep-learning tool for genomic-scale, strand-sensitive and single-nucleotide based detection of DNA modifications☆104Updated 2 years ago
- List of genome assembly tools☆65Updated last week
- a tool for inferring species tree from sequencing reads☆150Updated 3 months ago
- Renders a collection of sequences into a pangenome graph. https://doi.org/10.1093/bioinformatics/btae609.☆88Updated this week
- ☆14Updated last year
- Detecting methylation using signal-level features from Nanopore sequencing reads of plants☆60Updated 11 months ago
- The first deep learning based Nanopore simulator which can simulate the process of Nanopore sequencing.☆121Updated 4 years ago
- ClairS - a deep-learning method for long-read somatic small variant calling☆84Updated this week
- A dataset of real DNA traces for benchmarking trace reconstruction algorithms☆18Updated 6 months ago
- Codes and results from ONT dRNA benchmarking☆11Updated last year
- RNA modifications detection from Nanopore dRNA-Seq data☆84Updated 2 weeks ago
- Fast and flexible ORF finder☆69Updated 3 years ago
- ✂️ Deep learning-based splice site predictor that improves spliced alignments☆52Updated 3 months ago
- Eukaryotic Genome Annotation Pipeline-External caller scripts and documentation☆136Updated this week
- ClairS-TO - a deep-learning method for tumor-only somatic variant calling☆62Updated 2 months ago
- Nanopore basecalling and consensus decoding☆46Updated 2 years ago
- Align multiple amino acid or nucleotide sequences.☆60Updated 4 years ago
- Catalog of genomic indexes freely available from public clouds☆60Updated last month
- WDL’s and Dockerfiles for assembly QC process☆67Updated 2 weeks ago
- NEAT (NExt-generation Analysis Toolkit) simulates next-gen sequencing reads and can learn simulation parameters from real data.☆56Updated last week
- Training models for basecalling Oxford Nanopore reads☆115Updated 3 years ago
- NANOME pipeline (Nanopore long-read sequencing data consensus DNA methylation detection)☆30Updated last year
- Evaluation and polishing workflows for T2T genome assemblies☆130Updated 7 months ago
- DeepEdit: single-molecule detection and phasing of A-to-I RNA editing events using Nanopore direct RNA sequencing☆17Updated 2 years ago