Skip to content
Open
Changes from all commits
Commits
File filter

Filter by extension

Filter by extension

Conversations
Failed to load comments.
Loading
Jump to
Jump to file
Failed to load files.
Loading
Diff view
Diff view
3 changes: 3 additions & 0 deletions README.md
Original file line number Diff line number Diff line change
Expand Up @@ -65,6 +65,7 @@ List of software packages for Nanopore sequencing data analysis, including basec

- [minimap2](https://github.com/lh3/minimap2) - [C] - [Minimap2: pairwise alignment for nucleotide sequences](https://academic.oup.com/bioinformatics/article/34/18/3094/4994778)
- [Winnowmap](https://github.com/marbl/winnowmap) - [C] - [Weighted minimizer sampling improves long read mapping](https://academic.oup.com/bioinformatics/article/36/Supplement_1/i111/5870473)
- [NGMLR](https://github.com/philres/ngmlr) - [C++] - [Long-read mapper designed to align PacBio or Oxford Nanopore reads to a reference genome with a focus on reads that span structural variations](https://www.nature.com/articles/s41592-018-0001-7)

### Signal analysis

Expand Down Expand Up @@ -102,6 +103,7 @@ List of software packages for Nanopore sequencing data analysis, including basec
- [Clair3](https://github.com/HKU-BAL/Clair3) - [Python/C++] - [Clair3-RNA: a deep learning-based small variant caller for long-read RNA sequencing data](https://www.nature.com/articles/s41467-025-67237-y)
- [Sniffles](https://github.com/fritzsedlazeck/sniffles) - [Python] - [Detection of mosaic and population-level structural variants with Sniffles2](https://www.nature.com/articles/s41587-023-02024-y)
- [whatshap](https://github.com/whatshap/whatshap) - [Python/C++] - [Read-Based Phasing and Analysis of Phased Variants with WhatsHap](https://link.springer.com/protocol/10.1007/978-1-0716-2819-5_8)
- [LongPhase](https://github.com/twolinin/longphase) - [C] - [An ultra-fast program for simultaneously co-phasing SNPs, small indels, large SVs, and (5mC) modifications for Nanopore and PacBio platforms](https://academic.oup.com/bioinformatics/article/38/7/1816/6519151)

### Modification analysis

Expand All @@ -115,6 +117,7 @@ List of software packages for Nanopore sequencing data analysis, including basec
- [mCaller](https://github.com/al-mcintyre/mCaller) - [Python] - [Single-molecule sequencing detection of N6-methyladenine in microbial reference materials](https://www.nature.com/articles/s41467-019-08289-9).
- [DeepSignals](https://github.com/bioinfomaticsCSU/deepsignal) - [Python] - [DeepSignal: detecting DNA methylation state from Nanopore sequencing reads using deep-learning](https://academic.oup.com/bioinformatics/article/35/22/4586/5474907).
- [NanoMod](https://github.com/WGLab/NanoMod) - [Python] - [NanoMod: a computational tool to detect DNA modifications using Nanopore long-read sequencing data](https://bmcgenomics.biomedcentral.com/articles/10.1186/s12864-018-5372-8).
- [MethQC](https://github.com/JMencius/methqc) - [Python] - Quality control for DNA methylation detection in long-read sequencing.

#### RNA modification analysis

Expand Down