Evidence map›Paper›PMID 35255082›Full record

ArticlePLoS computational biology2022

Constructing benchmark test sets for biological sequence analysis using independent set algorithms.

Samantha Petti, Sean R Eddy

Erratum issuedAbstract 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. An erratum has been issued. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing 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

13 citing papers in PubMed.

  1. Article
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  11. Article
  12. From sequence to function through structure: Deep learning for protein design.Computational and structural biotechnology journal · 2023
    Review
  13. Phage family classification underFrontiers in microbiology · 2022
    Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

2 authors.

Samantha PettiNSF-Simons Center for the Mathematical and Statistical Analysis of Biology, Harvard University, Cambridge, Massachusetts, United States of America.ORCID 0000-0001-8281-8161
Sean R EddyHoward Hughes Medical Institute; Department of Molecular & Cellular Biology; and John A. Paulson School of Engineering and Applied Sciences, Harvard University, Cambridge, Massachusetts, United States of America.ORCID 0000-0001-6676-4706

Funding

HMMER and Infernal: Finding distant homologs of sequences and RNA structuresR01HG009116 · NHGRI · HARVARD UNIVERSITY · PI EDDY, SEAN R · 2016 to 2025
$4.3M
NHGRI NIH HHS R01 HG009116
6 · The paper itself

Abstract

Biological sequence families contain many sequences that are very similar to each other because they are related by evolution, so the strategy for splitting data into separate training and test sets is a nontrivial choice in benchmarking sequence analysis methods. A random split is insufficient because it will yield test sequences that are closely related or even identical to training sequences. Adapting ideas from independent set graph algorithms, we describe two new methods for splitting sequence data into dissimilar training and test sets. These algorithms input a sequence family and produce a split in which each test sequence is less than p% identical to any individual training sequence. These algorithms successfully split more families than a previous approach, enabling construction of more diverse benchmark datasets.

Indexed as

AlgorithmsSequence Analysis

Identifiers

PMID35255082
PMCPMC8929697

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.