ArticleBioinformatics advances2025
Atlantool: a command line tool to retrieve DNA and RNA sequencing reads from BAM files by the read identifier.
Article in Bioinformatics advances, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
What it found
Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.
The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
0 citing papers in PubMed.
No citing paper in PubMed yet.
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
10 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Motivation: DNA or RNA sequencing produce a large volume of data that is usually stored in a Binary Alignment Map (BAM) file format. Processing and analysis of this large genomic data require specialized software tools. The majority of processing requirements involve accessing DNA or RNA data by chromosomal co-ordinates using SAMtools or similar software. However, challenges arise where accessing the data by the sequencing read identifier is required, and as yet there is no reliable, efficient method or tool to do this. Here we present Atlantool, a fast software that can retrieve sequencing reads from a BAM file by the read identifier. Retrieval of sequencing reads using Atlantool requires a simple command line command similar to SAMtools. After a one-time creation of a read identifier index in the same BGZF format as BAM files, retrieval of data by the read identifier appears to be instantaneous. The sequencing reads can be of any length. Atlantool fills the existing need for a reliable tool to efficiently retrieve specific records from high volume DNA or RNA sequencing data and will enable new genomic analyses to be envisaged and carried out. Availability and implementation: Precompiled Atlantool executables are freely available for download from https://github.com/VCCRI/atlantool/releases for Linux, macOS, and Windows platforms, as is a Java JAR file that permits Atlantool to run in a Java environment. The source code and user documentation are available at https://github.com/VCCRI/atlantool/.
Identifiers
What Socratic holds
Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.