An accelerated framework for the classification of biological targets from solid-state micropore data. Issue 134 (October 2016)
- Record Type:
- Journal Article
- Title:
- An accelerated framework for the classification of biological targets from solid-state micropore data. Issue 134 (October 2016)
- Main Title:
- An accelerated framework for the classification of biological targets from solid-state micropore data
- Authors:
- Hanif, Madiha
Hafeez, Abdul
Suleman, Yusuf
Mustafa Rafique, M.
Butt, Ali R.
Iqbal, Samir M. - Abstract:
- Highlights: Micro/nanoscale devices that detect biological targets especially for early cancer diagnosis generate large datasets. Challenges like high background noise, slow analysis, and low signal-to-noise ratio make data analysis significantly tedious. A novel algorithm is implemented on GPU that automates the rapid detection of biological targets in larger datasets. The machine-learning approach records events, computes features and classifies future pulses into their respective types. The approach detects cells with an accuracy of 70% and demonstrates a speedup of 3-4X over serial implementation. Abstract: Micro- and nanoscale systems have provided means to detect biological targets, such as DNA, proteins, and human cells, at ultrahigh sensitivity. However, these devices suffer from noise in the raw data, which continues to be significant as newer and devices that are more sensitive produce an increasing amount of data that needs to be analyzed. An important dimension that is often discounted in these systems is the ability to quickly process the measured data for an instant feedback. Realizing and developing algorithms for the accurate detection and classification of biological targets in realtime is vital. Toward this end, we describe a supervised machine-learning approach that records single cell events (pulses), computes useful pulse features, and classifies the future patterns into their respective types, such as cancerous/non-cancerous cells based on the trainingHighlights: Micro/nanoscale devices that detect biological targets especially for early cancer diagnosis generate large datasets. Challenges like high background noise, slow analysis, and low signal-to-noise ratio make data analysis significantly tedious. A novel algorithm is implemented on GPU that automates the rapid detection of biological targets in larger datasets. The machine-learning approach records events, computes features and classifies future pulses into their respective types. The approach detects cells with an accuracy of 70% and demonstrates a speedup of 3-4X over serial implementation. Abstract: Micro- and nanoscale systems have provided means to detect biological targets, such as DNA, proteins, and human cells, at ultrahigh sensitivity. However, these devices suffer from noise in the raw data, which continues to be significant as newer and devices that are more sensitive produce an increasing amount of data that needs to be analyzed. An important dimension that is often discounted in these systems is the ability to quickly process the measured data for an instant feedback. Realizing and developing algorithms for the accurate detection and classification of biological targets in realtime is vital. Toward this end, we describe a supervised machine-learning approach that records single cell events (pulses), computes useful pulse features, and classifies the future patterns into their respective types, such as cancerous/non-cancerous cells based on the training data. The approach detects cells with an accuracy of 70% from the raw data followed by an accurate classification when larger training sets are employed. The parallel implementation of the algorithm on graphics processing unit (GPU) demonstrates a speedup of three to four folds as compared to a serial implementation on an Intel Core i7 processor. This incredibly efficient GPU system is an effort to streamline the analysis of pulse data in an academic setting. This paper presents for the first time ever, a non-commercial technique using a GPU system for realtime analysis, paired with biological cluster targeting analysis. … (more)
- Is Part Of:
- Computer methods and programs in biomedicine. Issue 134(2016)
- Journal:
- Computer methods and programs in biomedicine
- Issue:
- Issue 134(2016)
- Issue Display:
- Volume 134, Issue 134 (2016)
- Year:
- 2016
- Volume:
- 134
- Issue:
- 134
- Issue Sort Value:
- 2016-0134-0134-0000
- Page Start:
- 53
- Page End:
- 67
- Publication Date:
- 2016-10
- Subjects:
- Cancer detection -- Pattern detection and classification -- Run-time systems -- Human cells -- Solid-state micropores/nanopores
Medicine -- Computer programs -- Periodicals
Biology -- Computer programs -- Periodicals
Computers -- Periodicals
Medicine -- Periodicals
Médecine -- Logiciels -- Périodiques
Biologie -- Logiciels -- Périodiques
Biology -- Computer programs
Medicine -- Computer programs
Periodicals
Electronic journals
610.28 - Journal URLs:
- http://www.sciencedirect.com/science/journal/01692607 ↗
http://www.elsevier.com/journals ↗ - DOI:
- 10.1016/j.cmpb.2016.06.001 ↗
- Languages:
- English
- ISSNs:
- 0169-2607
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3394.095000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 406.xml