Evidence map›Paper›PMID 33794760›Full record

ArticleBMC bioinformatics2021

HARVESTMAN: a framework for hierarchical feature learning and selection from whole genome sequencing data.

Trevor S Frisby, Shawn J Baker, Guillaume Marçais, Quang Minh Hoang, Carl Kingsford, Christopher J Langmead

Abstract read
In one paragraph

Article in BMC bioinformatics, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
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4 · The record

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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.

Trevor S Frisby *Computational Biology Department, Carnegie Mellon University, Pittsburgh, PA, USA.
Shawn J Baker *Computational Biology Department, Carnegie Mellon University, Pittsburgh, PA, USA.
Guillaume MarçaisComputational Biology Department, Carnegie Mellon University, Pittsburgh, PA, USA.
Quang Minh HoangComputer Science Department, Carnegie Mellon University, Pittsburgh, PA, USA.
Carl KingsfordComputational Biology Department, Carnegie Mellon University, Pittsburgh, PA, USA. carlk@cs.cmu.edu.
Christopher J LangmeadComputational Biology Department, Carnegie Mellon University, Pittsburgh, PA, USA. cjl@cs.cmu.edu.ORCID http://orcid.org/0000-0001-7521-6736

Funding

VECTOR CORE FACILITYP30CA047904 · NCI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI Jessie Nedrow · 1988 to 2026
$158.0M
Integrated Interdisciplinary, inter-university PhD Program Computational Biology (T32)T32EB009403 · NIBIB · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI BAHAR, IVET, BAR-JOSEPH, ZIV · 2009 to 2023
$4.4M
Data Discovery: Computational Methods for Searching Short-Read Sequencing Experiments - Administrative SupplementR01GM122935 · NIGMS · CARNEGIE-MELLON UNIVERSITY · PI KINGSFORD, CARLETON LEE · 2017 to 2021
$1.2M
Gordon and Betty Moore Foundation GBMF4554NCI NIH HHS P30 CA047904NCI NIH HHS P30CA047904NIBIB NIH HHS T32 EB009403NIGMS NIH HHS R01 GM122935NIH HHS R01GM122935NIH HHS T32 EB009403PA DOH CURE grant 4100070287
6 · The paper itself

Abstract

backgroundSupervised learning from high-throughput sequencing data presents many challenges. For one, the curse of dimensionality often leads to overfitting as well as issues with scalability. This can bring about inaccurate models or those that require extensive compute time and resources. Additionally, variant calls may not be the optimal encoding for a given learning task, which also contributes to poor predictive capabilities. To address these issues, we present HARVESTMAN, a method that takes advantage of hierarchical relationships among the possible biological interpretations and representations of genomic variants to perform automatic feature learning, feature selection, and model building.

resultsWe demonstrate that HARVESTMAN scales to thousands of genomes comprising more than 84 million variants by processing phase 3 data from the 1000 Genomes Project, one of the largest publicly available collection of whole genome sequences. Using breast cancer data from The Cancer Genome Atlas, we show that HARVESTMAN selects a rich combination of representations that are adapted to the learning task, and performs better than a binary representation of SNPs alone. We compare HARVESTMAN to existing feature selection methods and demonstrate that our method is more parsimonious-it selects smaller and less redundant feature subsets while maintaining accuracy of the resulting classifier.

conclusionHARVESTMAN is a hierarchical feature selection approach for supervised model building from variant call data. By building a knowledge graph over genomic variants and solving an integer linear program , HARVESTMAN automatically and optimally finds the right encoding for genomic variants. Compared to other hierarchical feature selection methods, HARVESTMAN is faster and selects features more parsimoniously.

Indexed as

Breast NeoplasmsDeep LearningWhole Genome SequencingGenomeGenomicsHumansFeature selectionHierarchical feature spacesInteger linear programmingKnowledge graphsMachine learning

Identifiers

PMID33794760
PMCPMC8017869

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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.