Evidence map›Paper›PMID 35255084›Full record

ArticlePLoS computational biology2022

Model-based identification of conditionally-essential genes from transposon-insertion sequencing data.

Vishal Sarsani, Berent Aldikacti, Shai He, Rilee Zeinert, Peter Chien, Patrick Flaherty

Open access · goldAbstract read
In one paragraph

Article in PLoS computational biology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.4field-weighted citation impact, top 43% 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

3 citing papers in PubMed, 5 citations in OpenAlex.

  1. Article
  2. Article
  3. 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

6 authors at 2 institutions in 1 country.

Vishal SarsaniDepartment of Mathematics and Statistics, University of Massachusetts Amherst, Amherst, Massachusetts, United States of America.ORCID 0000-0002-9272-3438
Berent AldikactiDepartment of Biochemistry and Molecular Biology, University of Massachusetts Amherst, Amherst, Massachusetts, United States of America.ORCID 0000-0002-8916-8007
Shai HeDepartment of Mathematics and Statistics, University of Massachusetts Amherst, Amherst, Massachusetts, United States of America.
Rilee ZeinertDivision of Molecular and Cellular Biology, Eunice Kennedy Shriver National Institute of Child Health and Human Development, Bethesda, Maryland, United States of America.
Peter ChienDepartment of Biochemistry and Molecular Biology, University of Massachusetts Amherst, Amherst, Massachusetts, United States of America.
Patrick FlahertyDepartment of Mathematics and Statistics, University of Massachusetts Amherst, Amherst, Massachusetts, United States of America.ORCID 0000-0001-6097-6572
University of Massachusetts Amherst · USEunice Kennedy Shriver National Institute of Child Health and Human Development · US

Funding

Regulated Proteolysisin Bacteria Development and Stress ResponseR35GM130320 · NIGMS · UNIVERSITY OF MASSACHUSETTS AMHERST · PI Peter Chien · 2019 to 2026
$3.4M
Chemistry-Biology Interface Predoctoral Training GrantT32GM139789 · NIGMS · UNIVERSITY OF MASSACHUSETTS AMHERST · PI ERIC Robert STRIETER · 2021 to 2026
$3.4M
Learning Conditionally Essential Genetic Networks in the Protein Homeostasis System R01GM135931 · NIGMS · UNIVERSITY OF MASSACHUSETTS AMHERST · PI FLAHERTY, PATRICK · 2019 to 2021
$693k
NIGMS NIH HHS R01 GM135931NIGMS NIH HHS R35 GM130320NIGMS NIH HHS T32 GM139789
6 · The paper itself

Abstract

The understanding of bacterial gene function has been greatly enhanced by recent advancements in the deep sequencing of microbial genomes. Transposon insertion sequencing methods combines next-generation sequencing techniques with transposon mutagenesis for the exploration of the essentiality of genes under different environmental conditions. We propose a model-based method that uses regularized negative binomial regression to estimate the change in transposon insertions attributable to gene-environment changes in this genetic interaction study without transformations or uniform normalization. An empirical Bayes model for estimating the local false discovery rate combines unique and total count information to test for genes that show a statistically significant change in transposon counts. When applied to RB-TnSeq (randomized barcode transposon sequencing) and Tn-seq (transposon sequencing) libraries made in strains of Caulobacter crescentus using both total and unique count data the model was able to identify a set of conditionally beneficial or conditionally detrimental genes for each target condition that shed light on their functions and roles during various stress conditions.

Indexed as

DNA Transposable ElementsGenes, EssentialBayes TheoremHigh-Throughput Nucleotide SequencingMutagenesis, InsertionalDNA Transposable Elements

Identifiers

PMID35255084
PMCPMC8929702
OpenAlexW4220825712

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.