Related Experiment Video
Updated: Mar 15, 2026

11:26
Sequencing of mRNA from Whole Blood using Nanopore Sequencing
Published on: June 3, 2019
14.9K
Nanocall: an open source basecaller for Oxford Nanopore sequencing data.
Matei David1, L J Dursi1, Delia Yao1
1Ontario Institute for Cancer Research, Toronto M5G 0A3, Canada.
Bioinformatics (Oxford, England)
|September 11, 2016
Summary
Nanocall is the first open-source, offline basecaller for Oxford Nanopore MinION sequencing data. This free tool enables private analysis of genome sequencing data without an internet connection, offering comparable read identity to cloud-based platforms.
Area of Science:
- Genomics
- Bioinformatics
- Computational Biology
Background:
- The Oxford Nanopore MinION sequencer facilitates field-based genome sequencing.
- Current MinION data analysis relies on the cloud-based Metrichor platform for basecalling.
- There is a need for offline and private analysis solutions for MinION data.
Purpose of the Study:
- To develop an open-source, offline basecaller for Oxford Nanopore MinION sequencing data.
- To provide a freely available alternative to cloud-based basecalling solutions.
- To enable private and efficient analysis of MinION sequencing data.
Main Methods:
- Development of Nanocall, a novel open-source basecaller.
- Testing Nanocall on E.coli and human samples using R7.3 chemistry.
- Evaluation of Nanocall's read identity, efficiency, and processing speed.
Main Results:
- Nanocall achieves approximately 68% read identity, comparable to Metrichor's 1D data.
- The basecaller processes approximately 2500 Kbp per core hour, demonstrating high efficiency.
- Real-time basecalling of a MinION run was achieved on a 4-core desktop computer.
Conclusions:
- Nanocall is the first freely available, open-source, offline basecaller for Oxford Nanopore sequencing.
- The software enables private and efficient analysis of MinION data.
- Future development will focus on integrating 2D read capabilities.
Related Concept Videos
RNA-seq
12.4K
RNA sequencing, or RNA-Seq, is a high-throughput sequencing technology used to study the transcriptome of a cell. Transcriptomics helps to interpret the functional elements of a genome and identify the molecular constituents of an organism. Additionally, it also helps in understanding the development of an organism and the occurrence of diseases.
Before the discovery of RNA-seq, microarray-based methods and Sanger sequencing were used for transcriptome analysis. However, while...
Before the discovery of RNA-seq, microarray-based methods and Sanger sequencing were used for transcriptome analysis. However, while...
12.4K
Sanger Sequencing
777.3K
DNA sequencing is a fundamental technique that is routinely used in the biological sciences. This method can be applied to a range of questions at different scales - from the sequencing of a cloned DNA fragment or the study of a mutation in a gene up to whole-genome sequencing. However, despite the widespread use of sequencing today, it was not until 1977 that Fredrick Sanger and his collaborators developed the chain-termination method to decode DNA sequences. It relies on the separation of a...
777.3K

