Computational tools for copy number variation (CNV) detection using next-generation sequencing data: features and perspectives

Copy number variation (CNV) is a prevalent form of critical genetic variation that leads to an abnormal number of copies of large genomic regions in a cell. Microarray-based comparative genome hybridization (arrayCGH) or genotyping arrays have been standard technologies to detect large regions subje...

Celý popis

Uložené v:

Podrobná bibliografia
Vydané v:	BMC bioinformatics Ročník 14; číslo Suppl 11; s. S1
Hlavní autori:	Zhao, Min, Wang, Qingguo, Wang, Quan, Jia, Peilin, Zhao, Zhongming
Médium:	Journal Article
Jazyk:	English
Vydavateľské údaje:	London BioMed Central 13.09.2013 Springer Nature B.V
Predmet:	Algorithms Bioinformatics Biomedical and Life Sciences Computational Biology/Bioinformatics Computer Appl. in Life Sciences DNA Copy Number Variations Exons Genetic diversity Genome Genomics - methods Genotype High-Throughput Nucleotide Sequencing - methods Humans Life Sciences Microarrays Whole Genome Sequencing Data Copy Number Variation Region Copy Number Variation Circular Binary Segmentation Whole Exome Sequencing
ISSN:	1471-2105, 1471-2105
On-line prístup:	Získať plný text
Tagy:	Pridať tag Žiadne tagy, Buďte prvý, kto otaguje tento záznam!

Buďte prvý, kto okomentuje tento záznam!