Evidence map›Paper›PMID 40661418›Full record

ArticlebioRxiv : the preprint server for biology2025

Analysis of 3'-seq data from multiple

Quinlan Furumo, Michelle M Meyer

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

2 authors.

Quinlan FurumoBoston College, Department of Biology, Chestnut Hill MA 02467.
Michelle M MeyerBoston College, Department of Biology, Chestnut Hill MA 02467.

Funding

Using Fitness Landscapes to assess RNA Structure-Function Relationships From Inside the CellR01GM134259 · NIGMS · BOSTON COLLEGE · PI MEYER, MICHELLE MARGARET · 2020 to 2023
$1.6M
Interactions between translation inhibiting antibiotics and diverse RNA regulatory mechanism in pathogenic bacteria affect drug sensitivityR21AI148895 · NIAID · BOSTON COLLEGE · PI MEYER, MICHELLE MARGARET, VAN OPIJNEN, TIM · 2020 to 2021
$430k
NIAID NIH HHS R21 AI148895NIGMS NIH HHS R01 GM134259
6 · The paper itself

Abstract

3-prime end sequencing (3'-seq) is a high-throughput sequencing technique that is used to specifically quantify the changes in 3'-end formation of transcripts in bacterial cells, which is increasingly being utilized to address fundamental questions regarding transcription termination and pausing across a range of different bacterial species. However, the growing number of 3'-seq studies is accompanied by an increase in study-specific 3'-seq data analysis approaches. Thus, differences in a number of factors including: experimental design, data collection approaches, analysis methodologies, and interpretation decisions, make it challenging to confidently compare results derived from different studies, even those that were performed on the same organism. To assess the potential severity of these discrepancies, we used PIPETS, a statistically robust and genome-annotation agnostic 3'-seq analysis package, to study

Indexed as

3’-end sequencingEscherichia coliPIPETSsequencing analysisTerm-seq

Identifiers

PMID40661418
PMCPMC12259150

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.