Evidence map›Paper›PMID 35551337›Full record

ArticleBioinformatics (Oxford, England)2022

Exodus: sequencing-based pipeline for quantification of pooled variants.

Ilya Vainberg-Slutskin, Noga Kowalsman, Yael Silberberg, Tal Cohen, Jenia Gold, Edith Kario, Iddo Weiner, Inbar Gahali-Sass, Sharon Kredo-Russo, Naomi B Zak and 1 more

Abstract read
In one paragraph

Article in Bioinformatics (Oxford, England), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

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.

2 · The registry

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.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

11 authors.

Ilya Vainberg-SlutskinBiomX Ltd., Ness Ziona 7414002, Israel.
Noga KowalsmanBiomX Ltd., Ness Ziona 7414002, Israel.
Yael SilberbergBiomX Ltd., Ness Ziona 7414002, Israel.
Tal CohenBiomX Ltd., Ness Ziona 7414002, Israel.
Jenia GoldBiomX Ltd., Ness Ziona 7414002, Israel.
Edith KarioBiomX Ltd., Ness Ziona 7414002, Israel.
Iddo WeinerBiomX Ltd., Ness Ziona 7414002, Israel.ORCID 0000-0001-9554-346X
Inbar Gahali-SassBiomX Ltd., Ness Ziona 7414002, Israel.
Sharon Kredo-RussoBiomX Ltd., Ness Ziona 7414002, Israel.
Naomi B ZakBiomX Ltd., Ness Ziona 7414002, Israel.
Merav BassanBiomX Ltd., Ness Ziona 7414002, Israel.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

summaryNext-Generation Sequencing is widely used as a tool for identifying and quantifying microorganisms pooled together in either natural or designed samples. However, a prominent obstacle is achieving correct quantification when the pooled microbes are genetically related. In such cases, the outcome mostly depends on the method used for assigning reads to the individual targets. To address this challenge, we have developed Exodus-a reference-based Python algorithm for quantification of genomes, including those that are highly similar, when they are sequenced together in a single mix. To test Exodus' performance, we generated both empirical and in silico next-generation sequencing data of mixed genomes. When applying Exodus to these data, we observed median error rates varying between 0% and 0.21% as a function of the complexity of the mix. Importantly, no false negatives were recorded, demonstrating that Exodus' likelihood of missing an existing genome is very low, even if the genome's relative abundance is low and similar genomes are present in the same mix. Taken together, these data position Exodus as a reliable tool for identifying and quantifying genomes in mixed samples. Exodus is open source and free to use at: https://github.com/ilyavs/exodus. AVAILABILITY AND IMPLEMENTATION: Exodus is implemented in Python within a Snakemake framework. It is available on GitHub alongside a docker containing the required dependencies: https://github.com/ilyavs/exodus. The data underlying this article will be shared on reasonable request to the corresponding author. SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online.

Indexed as

High-Throughput Nucleotide SequencingSoftwareAlgorithmsGenomeResearch Design

Identifiers

PMID35551337
PMCPMC9191209

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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 OpenQuestion graph.