Evidence map›Paper›PMID 32029803›Full record

ArticleScientific reports2020

Identifying multi-hit carcinogenic gene combinations: Scaling up a weighted set cover algorithm using compressed binary matrix representation on a GPU.

Qais Al Hajri, Sajal Dash, Wu-Chun Feng, Harold R Garner, Ramu Anandakrishnan

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed, 1 pooled it
1.5field-weighted citation impact, top 19% 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

8 citing papers in PubMed, 1 synthesis or guideline pooled it, 18 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. 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

5 authors at 3 institutions in 1 country.

Qais Al Hajri *Department of Electrical and Computer Engineering, Virginia Tech, Blacksburg, VA, 24060, USA.
Sajal Dash *Department of Computer Science, Virginia Tech, Blacksburg, VA, 24060, USA.ORCID http://orcid.org/0000-0001-5308-914X
Wu-Chun FengDepartment of Electrical and Computer Engineering, Virginia Tech, Blacksburg, VA, 24060, USA.
Harold R GarnerDepartment of Biomedical Sciences, Edward Via College of Osteopathic Medicine, Blacksburg, VA, 24060, USA.
Ramu Anandakrishnan *Department of Biomedical Sciences, Edward Via College of Osteopathic Medicine, Blacksburg, VA, 24060, USA. ramu@vt.edu.ORCID http://orcid.org/0000-0003-0422-3984
Virginia Tech · USEdward Via College of Osteopathic Medicine · USSpartanburg Regional Healthcare System · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Despite decades of research, effective treatments for most cancers remain elusive. One reason is that different instances of cancer result from different combinations of multiple genetic mutations (hits). Therefore, treatments that may be effective in some cases are not effective in others. We previously developed an algorithm for identifying combinations of carcinogenic genes with mutations (multi-hit combinations), which could suggest a likely cause for individual instances of cancer. Most cancers are estimated to require three or more hits. However, the computational complexity of the algorithm scales exponentially with the number of hits, making it impractical for identifying combinations of more than two hits. To identify combinations of greater than two hits, we used a compressed binary matrix representation, and optimized the algorithm for parallel execution on an NVIDIA V100 graphics processing unit (GPU). With these enhancements, the optimized GPU implementation was on average an estimated 12,144 times faster than the original integer matrix based CPU implementation, for the 3-hit algorithm, allowing us to identify 3-hit combinations. The 3-hit combinations identified using a training set were able to differentiate between tumor and normal samples in a separate test set with 90% overall sensitivity and 93% overall specificity. We illustrate how the distribution of mutations in tumor and normal samples in the multi-hit gene combinations can suggest potential driver mutations for further investigation. With experimental validation, these combinations may provide insight into the etiology of cancer and a rational basis for targeted combination therapy.

Indexed as

AlgorithmsComputer GraphicsAntineoplastic Combined Chemotherapy ProtocolsBiomarkers, TumorCarcinogenesisComputational BiologyDatasets as TopicHumansMolecular Targeted TherapyMutationNeoplasmsOligonucleotide Array Sequence AnalysisPrecision MedicineTime FactorsBiomarkers, Tumor

Identifiers

PMID32029803
PMCPMC7005272
OpenAlexW3005024090

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.