Evidence map›Paper›PMID 35561201›Full record

ArticleBioinformatics (Oxford, England)2022

SASpector: analysis of missing genomic regions in draft genomes of prokaryotes.

Cédric Lood, Alejandro Correa Rojo, Deniz Sinar, Emma Verkinderen, Rob Lavigne, Vera van Noort

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

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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

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3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Cédric LoodDepartment of Microbial and Molecular Systems, KU Leuven, 3001 Leuven, Belgium.ORCID 0000-0001-7826-3378
Alejandro Correa RojoDepartment of Microbial and Molecular Systems, KU Leuven, 3001 Leuven, Belgium.
Deniz SinarDepartment of Microbial and Molecular Systems, KU Leuven, 3001 Leuven, Belgium.
Emma VerkinderenDepartment of Microbial and Molecular Systems, KU Leuven, 3001 Leuven, Belgium.
Rob LavigneDepartment of Biosystems, KU Leuven, 3001 Leuven, Belgium.
Vera van NoortDepartment of Microbial and Molecular Systems, KU Leuven, 3001 Leuven, Belgium.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

summaryMissing regions in short-read assemblies of prokaryote genomes are often attributed to biases in sequencing technologies and to repetitive elements, the former resulting in low sequencing coverage of certain loci and the latter to unresolved loops in the de novo assembly graph. We developed SASpector, a command-line tool that compares short-read assemblies (draft genomes) to their corresponding closed assemblies and extracts missing regions to analyze them at the sequence and functional level. SASpector allows to benchmark the need for resolved genomes, can be integrated into pipelines to control the quality of assemblies, and could be used for comparative investigations of missingness in assemblies for which both short-read and long-read data are available in the public databases. AVAILABILITY AND IMPLEMENTATION: SASpector is available at https://github.com/LoGT-KULeuven/SASpector. The tool is implemented in Python3 and available through pip and Docker (0mician/saspector). SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online.

Indexed as

High-Throughput Nucleotide SequencingSoftwareGenomeGenomicsSequence Analysis, DNA

Identifiers

PMID35561201
PMCPMC9113259

What OpenQuestion holds

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Registered trials

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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.