Evidence map›Paper›PMID 27474041›Full record

ArticleMedical & biological engineering & computing2017

Correlation-based feature selection and classification via regression of segmented chromosomes using geometric features.

Tanvi Arora, Renu Dhir

Abstract read
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Article in Medical & biological engineering & computing, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

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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.

Tanvi AroraDepartment of Computer Science and Engineering, Dr. B.R Ambedkar National Institute of Technology, Jalandhar, Punjab, India. tanviverma@rediffmail.com.
Renu DhirDepartment of Computer Science and Engineering, Dr. B.R Ambedkar National Institute of Technology, Jalandhar, Punjab, India.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The genetic defects in the humans are uncovered by studying the chromosomes, as they are the genetic information carriers. They are non-rigid objects and they appear in different orientations when they are imaged. To find out the genetic defects, the chromosomes are pre-processed so that they are not touching, overlapping, and bent, and the noise is also discarded. The presence of bends, overlaps, or touches makes it difficult to uncover the genetic abnormalities. So there is a need for development of an efficient technique to classify the segmented chromosomes into different types and then pre-process them in order to correct their orientation. In this work, a hybrid classification technique based upon correlation-based feature selection and classification via regression approach, which will classify the segmented chromosomes into five categories viz; straight, overlapping, bent, touching, or noise is presented. The performance evaluation has been done using 1592 segmented chromosomes from Advance Digital Imaging Research data set. The over-all accuracy of 94.78 % has been obtained for the five class problem. The performance of the proposed classifier has been compared with Bayes Net, Naïve Bayes, Radial Bias Feed Forward Network, and k-nearest-neighbour classifiers. Based upon this categorization, different pre-processing techniques will be applied to correct the orientation of the chromosomes.

Indexed as

Bayes TheoremChromosome AberrationsChromosomesGenetic Diseases, InbornHumansChromosomesClassificationFeature extractionFeature selectionGenetic defects

Identifiers

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Registered trials

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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.