Evidence map›Paper›PMID 19478015›Full record

ArticleBioinformatics (Oxford, England)2009

Family classification without domain chaining.

Jacob M Joseph, Dannie Durand

Open access · hybridAbstract read
In one paragraph

Article in Bioinformatics (Oxford, England), 2009. 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
0.8field-weighted citation impact, top 28% 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, 25 citations in OpenAlex.

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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 at 1 institution in 1 country.

Jacob M JosephDepartment of Biological and Computer Sciences, Carnegie Mellon University, Pittsburgh, PA 15213, USA. jacobmj@cmu.edu
Dannie Durand
Carnegie Mellon University · US

Funding

Spatial Patterning During DevelopmentP50GM071508 · NIGMS · PRINCETON UNIVERSITY · PI POWELL, SUSAN M · 2004 to 2013
$30.6M
NIGMS NIH HHS GM-071508NIGMS NIH HHS P50 GM071508
6 · The paper itself

Abstract

motivationClassification of gene and protein sequences into homologous families, i.e. sets of sequences that share common ancestry, is an essential step in comparative genomic analyses. This is typically achieved by construction of a sequence homology network, followed by clustering to identify dense subgraphs corresponding to families. Accurate classification of single domain families is now within reach due to major algorithmic advances in remote homology detection and graph clustering. However, classification of multidomain families remains a significant challenge. The presence of the same domain in sequences that do not share common ancestry introduces false edges in the homology network that link unrelated families and stymy clustering algorithms.

resultsHere, we investigate a network-rewiring strategy designed to eliminate edges due to promiscuous domains. We show that this strategy can reduce noise in and restore structure to artificial networks with simulated noise, as well as to the yeast genome homology network. We further evaluate this approach on a hand-curated set of multidomain sequences in mouse and human, and demonstrate that classification using the rewired network delivers dramatic improvement in Precision and Recall, compared with current methods. Families in our test set exhibit a broad range of domain architectures and sequence conservation, demonstrating that our method is flexible, robust and suitable for high-throughput, automated processing of heterogeneous, genome-scale data.

Indexed as

Sequence Homology, Amino AcidAnimalsComputational BiologyConserved SequenceDatabases, ProteinGenomeHumansMiceProteinsSequence Analysis, ProteinProteins

Identifiers

PMID19478015
PMCPMC2687961
OpenAlexW2133022970

What OpenQuestion holds

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LicenceCC BY-NC
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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.