Evidence map›Paper›PMID 30684135›Full record

ReviewJournal of applied genetics2019

A crash course in sequencing for a microbiologist.

Aleksandra Kozińska, Paulina Seweryn, Izabela Sitkiewicz

Open access · hybridAbstract readReview
In one paragraph

Review in Journal of applied genetics, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.5field-weighted citation impact, top 17% of its field
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

14 citing papers in PubMed, 28 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Review
  6. Review
  7. The Clinical View onFrontiers in microbiology · 2022
    Review
  8. Article
  9. Review
  10. Review
  11. Review
  12. Article
  13. Sulfation pathways from red to green.The Journal of biological chemistry · 2019
    Review
  14. Review
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

3 authors at 1 institution in 1 country.

Aleksandra KozińskaDepartment of Drug Biotechnology and Bioinformatics, National Medicines Institute, Chelmska 30/34, 00-725, Warszawa, Poland.
Paulina SewerynDepartment of Microbiology and Antibiotics, National Medicines Institute, Chelmska 30/34, 00-725, Warszawa, Poland.
Izabela SitkiewiczDepartment of Drug Biotechnology and Bioinformatics, National Medicines Institute, Chelmska 30/34, 00-725, Warszawa, Poland. i.sitkiewicz@nil.gov.pl.ORCID http://orcid.org/0000-0001-8228-9917
Narodowy Instytut Leków · PL

Funding

Fulbright Commission Senior Award 2018/2019Narodowe Centrum Nauki 2017/27/B/NZ7/00040
6 · The paper itself

Abstract

For the last 40 years, "Sanger sequencing" allowed to unveil crucial secrets of life. However, this method of sequencing has been time-consuming, laborious and remains expensive even today. Human Genome Project was a huge impulse to improve sequencing technologies, and unprecedented financial and human effort prompted the development of cheaper high-throughput technologies and strategies called next-generation sequencing (NGS) or whole genome sequencing (WGS). This review will discuss applications of high-throughput methods to study bacteria in a much broader context than simply their genomes. The major goal of next-generation sequencing for a microbiologist is not really resolving another circular genomic sequence. NGS started its infancy from basic structural and functional genomics, to mature into the molecular taxonomy, phylogenetic and advanced comparative genomics. Today, the use of NGS expended capabilities of diagnostic microbiology and epidemiology. The use of RNA sequencing techniques allows studying in detail the complex regulatory processes in the bacterial cells. Finally, NGS is a key technique to study the organization of the bacterial life-from complex communities to single cells. The major challenge in understanding genomic and transcriptomic data lies today in combining it with other sources of global data such as proteome and metabolome, which hopefully will lead to the reconstruction of regulatory networks within bacterial cells that allow communicating with the environment (signalome and interactome) and virtual cell reconstruction.

Indexed as

DNA, BacterialGenomicsHigh-Throughput Nucleotide SequencingHumansSequence Analysis, DNAWhole Genome SequencingDNA, BacterialMicrobiomeNext-generation sequencingPhylogenetic analysisSanger sequencingStructural genomicsTranscriptomics

Identifiers

PMID30684135
PMCPMC6373407
OpenAlexW2911948650

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.