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Discovery of large genomic inversions using long range information

BMC Genomics

Jan 12, 2017

Marzieh Eslami RasekhCan Alkan

Abstract

Although many algorithms are now available that aim to characterize different classes of structural variation, discovery of balanced rearrangements such as inversions remains an open problem. This is mainly due to the fact that breakpoints of such events typically lie within segmental d...read more

Mentioned in this Paper

Fluorescent Dyes
Fluorescent in Situ Hybridization
Sequence Inversion
Whole-Genome Shotgun Sequencing
Genome
Projections and Predictions
Segmental Duplications, Genomic
Inversion Mutation Abnormality
Nucleic Acid Sequencing
Genomics
35
49
Paper Details
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Discovery of large genomic inversions using long range information

BMC Genomics

Jan 12, 2017

Marzieh Eslami RasekhCan Alkan

PMID: 28073353

DOI: 10.1186/s12864-016-3444-1

Abstract

Although many algorithms are now available that aim to characterize different classes of structural variation, discovery of balanced rearrangements such as inversions remains an open problem. This is mainly due to the fact that breakpoints of such events typically lie within segmental d...read more

Mentioned in this Paper

Fluorescent Dyes
Fluorescent in Situ Hybridization
Sequence Inversion
Whole-Genome Shotgun Sequencing
Genome
Projections and Predictions
Segmental Duplications, Genomic
Inversion Mutation Abnormality
Nucleic Acid Sequencing
Genomics
35
49

Similar Papers Found In These Feeds

Fluorescence in situ Hybridization (FISH)

Fluorescence in situ hybridization (FISH) is one of the major techniques used to detect of chromosomal aberrations. Here is the latest research.

Chromosomal Duplication

Chromosomal duplication is a result of extra genetic material within the area of the chromosome. The duplication may have no effect or may be expressed in the phenotype of that individual. Some duplications are thought to be of evolutionary selection. Discover the latest research on chromosomal duplication here.

Related Papers

Bioinformatics

Identifying structural variants using linked-read sequencing data

BioinformaticsNovember 8, 2017
Rebecca ElyanowBenjamin J Raphael
Paper Details
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